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Assoc.Prof. Goonnapa Fucharoen

Assoc.Prof. Goonnapa Fucharoen

School of Medical Technology,
Faculty of Associated Medical Sciences,
Khon Kaen University
7003946836: H-INDEX 31
Education Level
  • ปริญญาตรี ()
  • ปริญญาโท ()
Expert
  • Thalassemia and related disorders

Documents

TCI อ้างอิงจาก http://www.tci-thaijo.org/

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SCOPUS

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PUBMED

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TCI

Title Author Year SCOPUS PUBMED ISI TCI
1. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies. Sedgewick, AE
Timofeev, N
Sebastiani, P
So, JC
Ma, ES
Chan, LC
Fucharoen, G
Fucharoen, S
Barbosa, CG
Vardarajan, BN
Farrer, LA
Baldwin, CT
Steinberg, MH
Chui, DH
0
2. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: a molecular and hematological analysis. Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Surapot, S
0
3. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand. Nuntakarn, L
Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Jetsrisuparb, A
Wiangnon, S
0
4. Thalassemia and hemoglobinopathies rather than iron deficiency are major causes of pregnancy-related anemia in northeast Thailand. Sanchaisuriya, K
Fucharoen, S
Ratanasiri, T
Sanchaisuriya, P
Fucharoen, G
Dietz, E
Schelp, FP
0
5. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis. Fucharoen, S
Fucharoen, G
Sae-ung, N
Sanchaisuriya, K
0
6. Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis. Pakdee, N
Yamsri, S
Fucharoen, G
Sanchaisuriya, K
Pissard, S
Fucharoen, S
0
7. A novel ochre mutation in the β-thalassemia gene of a Thai. Identification by direct cloning of the entire β-globin gene amplified using polymerase chain reaction Fucharoen, G.
Fucharoen, P.
Fukumaki, Y.
1989
8. A novel ochre mutation in the beta-thalassemia gene of a Thai. Identification by direct cloning of the entire beta-globin gene amplified using polymerase chain reactions. Fucharoen, S
Fucharoen, G
Fucharoen, P
Fukumaki, Y
1989
9. Heterogeneity of the γ-globin gene sequences in Japanese individuals: Implication of gene conversion in generation of polymorphisms Shiokawa, S
Fucharoen, S
Fucharoen, G
Tomatsu, S
Fukumaki, Y
1989
10. Molecular basis of beta-thalassemia in Thailand: analysis of beta-thalassemia mutations using the polymerase chain reaction. Fucharoen, G.
Laosombat, V.
Jetsrisuparb, A.
Tanphaichitr, V.S.
Suvatte, V.
Fukumaki, Y.
1989
11. A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe. Fucharoen, G.
Fukumaki, Y.
1990
12. Molecular basis of HbE-beta-thalassemia and the origin of HbE in northeast Thailand: identification of one novel mutation using amplified DNA from buffy coat specimens. Fucharoen, G.
Jetsrisuparb, A.
Fukumaki, Y.
1990
13. Molecular characterization and nonradioactive detection of beta-thalassemia in Malaysia Fucharoen, S
Fucharoen, G
Ata, K
Aziz, S
Hashim, S
Hassan, K
Fukumaki, Y
1990
14. Molecular heterogeneity of beta-thalassaemia in the Japanese: identification of two novel mutations. Fucharoen, G.
Fukumaki, Y.
1990
15. Simple non-radioactive method for detecting haemoglobin Constant Spring gene. Fucharoen, S.P.
Fucharoen, G.
Fukumaki, Y.
1990
16. Three-base deletion in exon 3 of the β-globin gene produced a novel variant (β gunma) with a thalassemia-like phenotype Fucharoen, S
Fucharoen, G
Fukumaki, Y
Nakayama, Y
Hattori, Y
Yamamoto, K
Ohba, Y
1990
17. Double heterozygosity of the β-Malay and a novel β-thalassemia gene in a Thai patient Fucharoen, S
Fucharoen, G
Laosombat, V
Fukumaki, Y
1991
18. Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait. Fucharoen, G
Fuchareon, S
Jetsrisuparb, A
Fukumaki, Y
1991
19. Eight-base deletion in exon 3 of the β-globin gene produced a novel variant (β Khon Kaen) with an inclusion body β-thalassemia trait [4] Fucharoen, G.
Fucharoen, S.P.
Jetsrisuparb, A.
Fukumaki, Y.
1991
20. Molecular basis of beta thalassemia in the south of Thailand. Laosombat, V.
Fucharoen, S.P.
Panich, V.
Fucharoen, G.
Nopparatana, C.
Fukumaki, Y.
1992
21. Molecular heterogeneity of beta-thalassemia in Thailand. Fukumaki, Y
Fucharoen, S
Fucharoen, G
Okamoto, N
Ichinose, M
Jetsrisuparb, A
Sriroongrueng, W
Nopparatana, C
Laosombat, V
Panich, V
1992
22. A simple non-radioactive assay for hemoglobin E gene in prenatal diagnosis Fucharoen, S
Fucharoen, G
Ratanasiri, T
Jetsrisuparb, A
Fukumaki, Y
1994
23. Rapid and simultaneous non-radioactive method for detecting alpha-thalassemia 1 (SEA type) and Hb Constant Spring genes. Fucharoen, G.
Fucharoen, S.P.
1994
24. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis. Fucharoen, S
Fucharoen, G
Ratanasiri, T
Jetsrisuparb, A
Fukumaki, Y
1995
25. Expression of hemoglobin E in newborn. Sae-Ung, N.
Fucharoen, G.
Fucharoen, S.P.
1995
26. Molecular basis of alpha (0)-thalassemia in northeast of Thailand. Fucharoen, G
Fucharoen, S
Wanhakit, C
Srithong, W
1995
27. mtDNA polymorphism in East Asian populations, with special reference to the peopling of Japan Horai, S
Murayama, K
Hayasaka, K
Matsubayashi, S
Hattori, Y
Fucharoen, G
Harihara, S
Park, KS
Omoto, K
Pan, IH
1996
28. Beta-globin gene haplotypes in some minor ethnic groups in Thailand. Fucharoen, G.
Fucharoen, S.P.
Chinoluck, P.
Khunsuk, S.
Sanchaisuriya, K.
Sae-Ung, N.
1997
29. Mitochondrial DNA polymorphism in East Asian populations with special reference to the peopling of Japan Fucharoen, G. 1997
30. Molecular and hematological characterization of HbE heterozygote with alpha-thalassemia determinant. Sanchaisuriya, K.
Fucharoen, G.
Sae-Ung, N.
Sae-ue, N.
Baisungneon, R.
Jetsrisuparb, A.
Fucharoen, S.P.
1997
31. Molecular and hematological characterization of HB tak and HB pyrgos in Thailand Fucharoen, S
Fucharoen, G
Sae-ung, N
Sanchaisuriya, K
Fukumaki, Y
1997
32. Atypical hemoglobin H disease in a Thai patient resulting from a combination of α-thalassemia 1 and hemoglobin constant spring with hemoglobin J Bangkok heterozygosity S Fucharoen
K Ayukarn
K Sanchaisuriya
G Fucharoen
2001
33. Mitochondrial DNA polymorphisms in Thailand. G Fucharoen
S Fucharoen
S Horai
2001
34. Molecular characterization of (δβ)°/β°-thalassemia and (δβ)°-thalassemia/hemoglobin E in Thai patients Fucharoen, S.P.
Pengjam, Y.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2001
35. Molecular characterization of (deltabeta)(0)/beta(0)-thalassemia and (deltabeta)(0)-thalassemia/hemoglobin E in Thai patients. Fucharoen, S
Pengjam, Y
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2001
36. Molecular characterization of (delta beta)degrees/beta degrees-thalassemia and (delta beta)degrees-thalassemia/hemoglobin E in Thai patients S Fucharoen
Y Pengjam
S Surapot
G Fucharoen
K Sanchaisuriya
2001
37. Molecular characterization of hemoglobin C in Thailand Sanchaisuriya, K.
Fucharoen, G.
Nattaya Sae-ung, N.
Siriratmanawong, I.
Surapot, S.
Fucharoen, S.P.
2001
38. Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients. S Fucharoen
K Sanchaisuriya
G Fucharoen
S Surapot
2001
39. Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients [1] Fucharoen, S.P.
Sanchaisuriya, K.
Fucharoen, G.
Surapot, S.
2001
40. Simultaneous PCR detection of beta-thalassemia and alpha-thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome Siriratmanawong, N
Fucharoen, G
Sanchaisuriya, K
Ratanasiri, T
Fucharoen, S
2001
41. A simplified screening for alpha-thalassemia 1 (SEA type) using a combination of a modified osmotic fragility test and a direct PCR on whole blood cell lysates Panyasai, S.
Sringam, P.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2002
42. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients. Y Changtrakun
S Fucharoen
K Ayukarn
N Siriratmanawong
G Fucharoen
K Sanchaisuriya
2002
43. Frequency Distribution and Haplotypic Heterogeneity of beta(E)-Globin Gene among Eight Minority Groups of Northeast Thailand. Fucharoen, G.
Fucharoen, S.P.
Sanchaisuriya, K.
Sae-Ung, N.
2002
44. Hb Paksé [(α2) codon 142 (TAA→TAT or Term→Tyr)] in Thai patients with EABart's disease and Hb H disease Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2002
45. Hb Paksé [(alpha2) codon 142 (TAA-->TAT or Term-->Tyr)J in Thai patients with EAbart's disease and Hb H Disease. Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2002
46. Hb Pakse [(alpha 2) codon 142(TAA -> TAT or Term -> Tyr)] in Thai patients with EABart's disease and Hb H disease K Sanchaisuriya
G Fucharoen
S Fucharoen
2002
47. Identification of Hb S in Thai patients Y Changtrakun
V Suksa-ard
G Fucharoen
K Sanchaisuriya
S Fucharoen
2002
48. Molecular analysis of a Thai β-thalassaemia heterozygote with normal haemoglobin A2 level: Implication for population screening S Fucharoen
G Fucharoen
K Sanchaisuriya
Y Pengjam
2002
49. Molecular and hematological characterization of HPFH-6/indian deletion-inversion Gγ(Aγδβ)O -Thalassemia and Gγ(Aγδβ)O -thalassemia/HbE in Thai patients Fucharoen, S.P.
Pengjam, Y.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2002
50. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients. S Fucharoen
Y Pengjam
S Surapot
G Fucharoen
K Sanchaisuriya
2002
51. Molecular characterization of Hb D-Punjab [β121(GH4)Glu → Gln] in Thailand Fucharoen, S.P.
Changtrakun, Y.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2002
52. Molecular characterization of Hb D-Punjab [beta 121(GH4)Glu -> Gln] in Thailand Fucharoen, S
Changtrakun, Y
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2002
53. Molecular characterization of thalassemia intermedia associated with HPFH-6/beta-thalassemia and HPFH-6/Hb E in Thai patients. S Fucharoen
G Fucharoen
K Sanchaisuriya
S Surapot
2002
54. Paternal relationships of modern Asian populations, as viewed from the human Y-chromosomal DNA variation A Tajima
IH Pan
G Fucharoen
S Fucharoen
M Matsuo
K Tokunaga
T Juji
M Hayami
K Omoto
S Horai
2002
55. Three major lineages of Asian Y chromosomes: Implications for the peopling of east and southeast Asia Tajima, A
Pan, IH
Fucharoen, G
Fucharoen, S
Matsuo, M
Tokunaga, K
Juji, T
Hayami, M
Omoto, K
Horai, S
2002
56. Triple heterozygosity of a hemoglobin variant: hemoglobin Pyrgos with other hemoglobinopathies. A Jetsrisuparb
K Sanchaisuriya
G Fucharoen
S Fucharoen
S Wiangnon
P Komwilaisak
2002
57. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family. S Fucharoen
Y Changtrakun
T Ratanasiri
G Fucharoen
K Sanchaisuriya
2003
58. Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families. Fucharoen, S.P.
Sanchaisuriya, K.
Fucharoen, G.
Panyasai, S.
2003
59. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of α-thalassemia in Thailand Sanchaisuriya, K
Fucharoen, G
Sae-ung, N
Jetsrisuparb, A
Fucharoen, S
2003
60. Non-invasive fetal sex determination using a conventional nested PCR analysis of fetal DNA in maternal plasma. Tungwiwat, W.
Fucharoen, G.
Ratanasiri, T.
Sanchaisuriya, K.
Fucharoen, S.P.
2003
61. Prenatal detection of fetal hemoglobin E gene from maternal plasma Fucharoen, G.
Tungwiwat, W.
Ratanasiri, T.
Sanchaisuriya, K.
Fucharoen, S.P.
2003
62. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia. Fucharoen, G.
Sanchaisuriya, K.
Sae-Ung, N.
Fucharoen, S.P.
2004
63. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand. S Chunpanich
K Ayukarn
K Sanchaisuriya
G Fucharoen
S Fucharoen
2004
64. Molecular and hematological characterization of hemoglobin Hope/hemoglobin E and hemoglobin Hope/alpha-thalassemia 2 in Thai patients. Chunpanich, S.
Fucharoen, S.P.
Sachaisuriya, K.
Fucharoen, G.
2004
65. Molecular basis and hematologic characterization of δβ- thalassemia and hereditary persistence of fetal hemoglobin in Thailand Panyasai, S.
Fucharoen, S.P.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2004
66. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand. S Panyasai
S Fucharoen
S Surapot
G Fucharoen
K Sanchaisuriya
2004
67. Multiplex allele-specific PCR assay for differential diagnosis of Hb S, Hb D-Punjab and Hb Tak. K Sanchaisuriya
S Chunpanich
G Fucharoen
S Fucharoen
2004
68. The diverse molecular basis and hematological features of Hb H and AEBart's diseases in Northeast Thailand. S Boonsa
K Sanchaisuriya
G Fucharoen
S Wiangnon
A Jetsrisuparb
S Fucharoen
2004
69. A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy - An alternative approach to electronic blood cell counting Sanchaisuriya, K
Fucharoen, S
Fucharoen, G
Ratanasiri, T
Sanchaisuriya, P
Changtrakul, Y
Ukosanakarn, U
Ussawaphark, W
Schelp, FP
2005
70. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy. K Sanchaisuriya
S Chunpanich
S Fucharoen
G Fucharoen
P Sanchaisuriya
Y Changtrakun
2005
71. Compound heterozygote state for Gγ Aγ(δβ)°-thalassemia and hereditary persistence of fetal hemoglobin Fucharoen, S.P.
Panyasai, S.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2005
72. Compound heterozygote state for (G)gamma(A)gamma(delta beta)degrees-thalassemia and hereditary persistence of fetal hemoglobin Fucharoen, S
Panyasai, S
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2005
73. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: A molecular and hematological analysis Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Surapot, S.
2005
74. Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients Fucharoen, S
Singsanan, S
Sanchaisuriya, K
Fucharoen, G
2005
75. Thalassemia intermedia associated with complex interaction of Hb Beijing [α16(A14)Lys→Asn] and Hb E [β26(B8)Glu→Lys] with a deletional α-thalassemia-1 in a Thai family Fucharoen, S.P.
Chunpanich, S.
Sanchaisuriya, K.
Fucharoen, G.
2005
76. Thalassemia intermedia associated with complex interaction of Hb Beijing [alpha 16(A14)Lys -> Asn] and Hb E [beta 26(B8)Glu -> Lys] with a deletional alpha-thalassemia-1 in a Thai family Fucharoen, S
Chunpanich, S
Sanchaisuriya, K
Fucharoen, G
Kunyanone, N
2005
77. Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma. Warunee Tungwiwat
Supan Fucharcoen
Goonnapa Fucharoen
Thawalwong Ratanasiri
Kanokwan Sanchaisuriya
2006
78. Development of severe anemia during fever episodes in patients with hemoglobin E trait and hemoglobin H disease combinations. A Jetsrisuparb
K Sanchaisuriya
G Fucharoen
S Fucharoen
S Wiangnon
C Jetsrisuparb
J Sirijirachai
K Chansoong
2006
79. Molecular and hematological profiles of hemoglobin EE disease with different forms of α-thalassemia G Fucharoen
J Trithipsombat
S Sirithawee
S Yamsri
Y Changtrakul
K Sanchaisuriya
S Fucharoen
2006
80. Thalassemia and hemoglobinopathies rather than iron deficiency are major causes of pregnancy-related anemia in northeast Thailand Sanchaisuriya, K.
Fucharoen, S.P.
Ratanasiri, T.
Sanchaisuriya, P.
Fucharoen, G.
Dietz, E.
Schelp, F.P.
2006
81. α0-Thalassemia and related disorders in northeast Thailand: A molecular and hematological characterization Sae-ung, N
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2007
82. α/β-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function Chaisue, C
Kitcharoen, S
Wilairat, P
Jetsrisuparb, A
Fucharoen, G
Fucharoen, S
2007
83. Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia. Warunee Tungwiwat
Goonnapa Fucharoen
Supan Fucharoen
Thawalwong Ratanasiri
Kanokwan Sanchaisuriya
Natraya Sae-Ung
2007
84. Coexistence of Southeast Asian ovalocytosis and β-thalassemia: A molecular and hematological analysis Fucharoen, G
Fucharoen, S
Singsanan, S
Sanchaisuriya, K
2007
85. Cutoff values of Hb E and MCV for screening of double heterozygosity for Hb E/alpha(0)-thalassemia Kanokwan Sanchaisuriya
Sunisa Chirakul
Hataichanok Srivorakun
Goonnapa Fucharoen
Yossombat Changtrakun
Supan Fucharoen
2007
86. Effect of the maternal βE-globin gene on hematologic responses to iron supplementation during pregnancy Sanchaisuriya, K
Fucharoen, S
Ratanasiri, T
Sanchaisuriya, P
Fucharoen, G
Dietz, E
Schelp, FP
2007
87. Evaluation of the fetal sex prediction using a conventional PCR analysis of DNA in maternal plasma Warunee Tungwiwat
Goonnapa Fucharoen
Supan Fucharoen
Thawalwong Ratanasiri
Kanokwan Sanchaisuriya
Nattaya Sae-Ung
2007
88. H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers. Yamsri, S.
Sanchaisuriya, K.
Fucharoen, S.P.
Fucharoen, G.
Jetsrisuparb, A.
Wiangnon, S.
Changtrakul, Y.
Sanchaisuriya, P.
2007
89. High prevalence of alpha thalassemia in Thai families with beta thalassemia: Molecular and hematological analysis Goonnapa Fucharoen
Yossombat Changtrakul
Kanokwan Sanchaisuriya
Nattaya Sae-Ung
Supan Fucharoen
Arunee Jetsrisuparb
2007
90. Molecular and hematological features of the Hb constant spring EE bart's disease Supan Fucharoen
Goonnapa Fucharoen
Nattaya Sae-Ung
Kanokwan Sanchaisuriya
2007
91. Molecular characterization and origins of Hb constant spring and Hb Pakse in Southeast Asian populations Sanita Singsanan
Goonnapa Fucharoen
Onekham Savongsy
Kanokwan Sanchaisuriya
Supan Fucharoen
2007
92. Molecular characterization and origins of Hb constant spring and Hb Paksé in Southeast Asian populations Singsanan, S
Fucharoen, G
Savongsy, O
Sanchaisuriya, K
Fucharoen, S
2007
93. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha degrees-thalassemia determinants Nirut Siriratmanawong
Charnchai Pinmuang-Ngam
Goonnapa Fucharoen
Supan Fucharoen
2007
94. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different αo-thalassemia determinants Siriratmanawong, N.
Fucharoen, G.
Fucharoen, S.P.
2007
95. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants. Siriratmanawong, N
Pinmuang-Ngam, C
Fucharoen, G
Fucharoen, S
2007
96. Rapid molecular characterization of Hb queens and Hb siam: Two variants easily misidentified as sickle Hb Fucharoen, S
Singsanan, S
Hama, A
Fucharoen, G
Sanchaisuriya, K
2007
97. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: A molecular and hematological analysis Supan Fucharoen
Goonnapa Fucharoen
Nattaya Sae-ung
Kanokwan Sanchaisuriya
2007
98. Accuracy of fetal gender detection using a conventional nested PCR assay of maternal plasma in daily practice Tungwiwat, W.
Fucharoen, S.P.
Fucharoen, G.
Ratanasiri, T.
Sanchaisuriya, K.
2008
99. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice using two PCR methods G. Fucharoen
R. Karnpean
S. Fucharoen
N. Sae-Ung
K. Sanchaisuriya
2008
100. BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Amanda E. Sedgewick
Nadia Timofeev
Paola Sebastiani
Jason C. C. So
Edmond S. K. Ma
Li Chong Chan
Goonnapa Fucharoen
Supan Fucharoen
Cynara G. Barbosa
Badri N. Vardarajan
Lindsay A. Farrer
Clinton T. Baldwin
Martin H. Steinberg
David H. K. Chui
2008
101. Effective screening for double heterozygosity of Hb E/α0 -thalassemia Kanokwan Sanchaisuriya
Sunisa Chirakul
Hataichanok Srivorakun
Goonnapa Fucharoen
Supan Fucharoen
Yossombat Changtrakul
Pattara Sanchaisuriya
2008
102. Effective screening for thalassemia and hemoglobinopathies among pregnant Laos women S. Fucharoen
O. Savongsy
G. Fucharoen
K. Sanchaisuriya
N. Sae-ung
2008
103. Effect of alpha (0)-thalassemia, beta-thalassemia and hemoglobin E genes on anemia: comparison between males and females S. Yamsri
K. Sanchaisuriya
G. Fucharoen
S. Fucharoen
N. Sae-ung
A. Jetsrisuparp
2008
104. H63D prevalence in Thais, Laotian and Cambodian subjects and its protecting effect on iron deficiency in pregnancy K. Sanchaisuriya
S. Yamsri
S. Fucharoen
G. Fucharoen
P. Sanchaisuriya
O. Savongse
R. Devenish
2008
105. Hemoglobin profiles and hematologic features of thalassemic newborns: Application to screening of α-thalassemia 1 and hemoglobin E Tritipsombut, J
Sanchaisuriya, K
Fucharoen, S
Fucharoen, G
Siriratmanawong, N
Pinmuang-ngam, C
Sanchaisuriya, P
2008
106. Interactions of Hb Q-Thailand with various hemoglobinopathies: molecular and hemoglobin analysis S. Singsanan
G. Fucharoen
S. Fucharoen
S. Yamsri
K. Sanchaisuriya
N. Sae-ung
2008
107. Stability of red blood cell parameters in carriers of alpha-thalassemia, beta-thalassemia and hemoglobin E N. Sae-ung
K. Soontornwisai
T. Junthakorn
G. Fucharoen
K. Sanchaisuriya
S. Fucharoen
2008
108. Thalassemia and hemoglobinopathies in pregnant Lao women: carrier screening, prevalence and molecular basis. Onekham Savongsy
Supan Fucharoen
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Nattaya Sae-ung
2008
109. Accurate Prenatal Diagnosis of Hb Bart's Hydrops Fetalis in Daily Practice with a Double-Check PCR System Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
Sae-Ung, N.
Sanchaisuriya, K.
Ratanasiri, T.
2009
110. Analysis of fetal blood using capillary electrophoresis system: A simple method for prenatal diagnosis of severe thalassemia diseases Srivorakun, H
Fucharoen, G
Sae-Ung, N
Sanchaisuriya, K
Ratanasiri, T
Fucharoen, S
2009
111. Complex interaction of Hb e [β26(B8)Glu→Lys], Hb Korle-Bu [β73(E17)Asp→Asn] and a deletional α-thalassemia-1 in pregnancy Siriratmanawong, N.
Chansri, W.
Singsanan, S.
Fucharoen, G.
Fucharoen, S.P.
2009
112. COMPLEX INTERACTION OF Hb E [beta 26(B8)Glu -> Lys], Hb KORLE-BU [beta 73(E17)Asp -> Asn] AND A DELETIONAL alpha-THALASSEMIA-1 IN PREGNANCY Siriratmanawong, N
Chansri, W
Singsanan, S
Fucharoen, G
Fucharoen, S
2009
113. EFFECT OF IRON FORTIFIED MILK ON HEMATOLOGICAL CHANGES IN NON-IRON DEFICIENT THAI-SCHOOL CHILDREN K. Sanchaisuriya
N. Panomai
P. Sanchaisuriya
S. Lowirakorn
S. Yamsri
G. Fucharoen
S. Fucharoen
F. Schelp
2009
114. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand Lalana Nuntakarn
Supan Fucharoen
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Arunee Jetsrisuparb
Surapon Wiangnon
2009
115. Prenatal Diagnosis of Hemoglobin Bart's Hydrops Fetalis with Gap-PCR System Response Rossarin Karnpean
Goonnapa Fucharoen
Supan Fucharoen
Nattaya Sae-ung
Kanokwan Sanchaisuriya
Thawalwong Ratanasiri
2009
116. Response to Dr. Dong-Zhi Li Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
Sae-Ung, N.
Sanchaisuriya, K.
Ratanasiri, T.
2009
117. Compound Heterozygous Hb TakHb e Causes Secondary Erythrocytosis in a Thai Family Teawtrakul, N.
Sirijirachai, C.
Chansung, G.
Chansung, G.
Fucharoen, G.
2010
118. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family. Nattiya Teawtrakul
Chittima Sirijirachai
Ganjana Chansung
Goonnapa Fucharoen
2010
119. Hemoglobin Q-Thailand related disorders: Origin, molecular, hematological and diagnostic aspects Singsanan, S
Karnpean, R
Fucharoen, G
Sanchaisuriya, K
Sae-Ung, N
Fucharoen, S
2010
120. Improvement of alpha(0) - Thalassemia Screening Using Combined Osmotic Fragility, Dichlorophenolindophenol and Hb H Inclusion Tests Chaibunruang, A
Pornphannukool, S
Sae-Ung, N
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2010
121. Improvement of αo-thalassemia screening using combined osmotic fragility, dichlorophenolindophenol and Hb H inclusion tests Chaibunruang, A.
Pornphannukool, S.
Sae-Ung, N.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2010
122. Interactions of hemoglobin Lepore (δβ hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis Chaibunruang, A.
Srivorakun, H.
Fucharoen, S.P.
Fucharoen, G.
Sae-Ung, N.
Sanchaisuriya, K.
2010
123. Interactions of hemoglobin Lepore (delta beta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis Chaibunruang, A
Srivorakun, H
Fucharoen, S
Fucharoen, G
Sae-ung, N
Sanchaisuriya, K
2010
124. Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Sae-Ung, N.
Ratanasiri, T.
Fucharoen, S.P.
2010
125. Secondary erythrocytosis caused by hemoglobin Tak/(δβ)0-thalassemia syndrome. Prakobkaew, N
Singsanan, S
Fucharoen, G
Surapot, S
Fucharoen, S
2010
126. Secondary erythrocytosis caused by hemoglobin Tak/(δβ)- thalassemia syndrome Prakobkaew, N.
Singsanan, S.
Fucharoen, G.
Surapot, S.
Fucharoen, S.P.
2010
127. Secondary Erythrocytosis Caused by Hemoglobin Tak/(delta beta)(0)-Thalassemia Syndrome Nattaphol Prakobkaew
Sanita Singsanan
Goonnapa Fucharoen
Satja Surapot
Supan Fucharoen
2010
128. Thalassemia and iron deficiency in a group of northeast Thai school children: relationship to the occurrence of anemia Panomai, N
Sanchaisuriya, K
Yamsri, S
Sanchaisuriya, P
Fucharoen, G
Fucharoen, S
Schelp, FP
2010
129. Anemia, iron deficiency and thalassemia among adolescents in Northeast Thailand: Results from two independent surveys Anupong Pansuwan
Goonnapa Fucharoen
Supan Fucharoen
Boonmee Himakhun
Samrit Dangwiboon
2011
130. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α +-thalassemia Srivorakun, H
Fucharoen, G
Puangplruk, R
Kheawon, N
Fucharoen, S
2011
131. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [alpha 63(E12)Ala -> Val], a novel alpha 2-globin chain variant with Hb E [beta 26(B8)Glu -> Lys] and a deletional alpha(+)-thalassemia Hataichanok Srivorakun
Goonnapa Fucharoen
Rawiwan Puangplruk
Napat Kheawon
Supan Fucharoen
2011
132. Evaluation of the URIT-2900 Automated Hematology Analyzer for screening of thalassemia and hemoglobinopathies in Southeast Asian populations Karnpean, R.
Pansuwan, A.
Fucharoen, G.
Fucharoen, S.P.
2011
133. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand. Supawadee Yamsri
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Nattaya Sae-ung
Supan Fucharoen
2011
134. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of β-thalassemia in northeast Thailand Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Sae-Ung, N.
Fucharoen, S.P.
2011
135. Hb phimai [β72(E16)Ser→Thr]: A novel β-globin structural variant found in association with Hb constant spring in pregnancy Singsanan, S
Srivorakun, H
Fucharoen, G
Puangplruk, R
Fucharoen, S
2011
136. Hb PHIMAI [beta 72(E16)Ser -> Thr]: A NOVEL beta-GLOBIN STRUCTURAL VARIANT FOUND IN ASSOCIATION WITH Hb CONSTANT SPRING IN PREGNANCY Sanita Singsanan
Hataichanok Srivorakun
Goonnapa Fucharoen
Rawiwan Puangplruk
Supan Fucharoen
2011
137. Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects Chaibunruang, A
Fucharoen, G
Jetsrisuparb, A
Fucharoen, S
2011
138. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system. G. Fucharoen
H. Srivorakun
S. Singsanan
S. Fucharoen
2011
139. Thalassemia and hemoglobinopathies in Southeast Asian newborns: diagnostic assessment using capillary electrophoresis system Srivorakun, H.
Fucharoen, G.
Changtrakul, Y.
Komwilaisak, P.
Fucharoen, S.P.
2011
140. A spurious haemoglobin A1c result associated with double heterozygote for haemoglobin Raleigh (β1[NA1]Val → Ala) and α+-thalassaemia Singha, K
Fucharoen, G
Chaibunruang, A
Netnee, P
Fucharoen, S
2012
141. A spurious haemoglobin A(1c) result associated with double heterozygote for haemoglobin Raleigh (beta 1[NA1]Val -> Ala) and alpha(+)-thalassaemia Kritsada Singha
Goonnapa Fucharoen
Attawut Chaibunruang
Paripat Netnee
Supan Fucharoen
2012
142. DEMONSTRATION OF HB CONSTANT SPRING AND HB E-CONSTANT SPRING ON CAPILLARY ELECTROPHORESIS SYSTEM Supawadee Yamsri
Patcharawadee Prayalaw
Nattaya Sae-ung
Goonnapa Fucharoen
Supan Fucharoen
2012
143. FETAL RED BLOOD CELLS PARAMETERS IN THALASSEMIA AND HB E RELATED DISORDERS Rossarin Karnpean
Goonnapa Fucharoen
Supan Fucharoen
2012
144. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals. Chaibunruang, A.
Fucharoen, G.
Fucharoen, S.P.
2012
145. FIRST DESCRIPTION OF A Hb A(2) VARIANT IN THAILAND. IDENTIFICATION OF Hb A(2)-MELBOURNE [delta 43(CD2)Glu -> Lys] IN THAI INDIVIDUALS Attawut Chaibunruang
Goonnapa Fucharoen
Supan Fucharoen
2012
146. Genetic origin and interaction of the Filipino beta(0)-thalassemia with Hb E and alpha-thalassemia in a Thai family Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2012
147. Genetic origin and interaction of the Filipino β⁰-thalassemia with Hb E and α-thalassemia in a Thai family. Yamsri, S
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2012
148. Hb H DISEASE WITH VARIOUS beta HEMOGLOBINOPATHIES: MOLECULAR, HEMATOLOGICAL AND DIAGNOSTIC ASPECTS Fucharoen, S
Fucharoen, G
2012
149. Micromapping of thalassemia and hemoglobinopathies in diferent regions of Northeast Thailand and Vientaine, Laos People's Democratic Republic Jaruwan Tritipsombut
Kanokwan Sanchaisuriya
Prachatip Phollarp
Dalouny Bouakhasith
Pattara Sanchaisuriya
Goonnapa Fucharoen
Supan Fucharoen
Frank P. Schelp
2012
150. Micromapping of thalassemia and hemoglobinopathies in diferent regions of northeast Thailand and Vientiane, Laos People's Democratic Republic. Tritipsombut, J
Sanchaisuriya, K
Phollarp, P
Bouakhasith, D
Sanchaisuriya, P
Fucharoen, G
Fucharoen, S
Schelp, FP
2012
151. Phenotypic expression of hemoglobins A(2), E and F in various hemoglobin E related disorders Sae-Ung, N.
Srivorakun, H.
Fucharoen, G.
Yamsri, S.
Sanchaisuriya, K.
Fucharoen, S.P.
2012
152. Phenotypic expression of hemoglobins A₂, E and F in various hemoglobin E related disorders. Sae-ung, N
Srivorakun, H
Fucharoen, G
Yamsri, S
Sanchaisuriya, K
Fucharoen, S
2012
153. PREVALENCE OF SOUTHEAST ASIAN OVALOCYTOSIS IN THAI POPULATION Lalitpatch Ngouprommin
Nattaya Sae-ung
Supan Fucharoen
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
2012
154. PROFICIENCY TESTING PROGRAM OF HEMOGLOBIN ANALYSIS FOR PREVENTION AND CONTROL OF THALASSEMIA IN THAILAND: 2 YEARS OF EXPERIENCE Anupong Pansuwan
Rossarin Karnpean
Goonnapa Fucharoen
Supan Fucharoen
2012
155. RAPID SCREENING FOR ALPHA(0)-THALASSEMIA (SEA AND THAI DELETIONS) USING A COMBINED OSMOTIC FRAGILITY TEST AND REAL-TIME PCR Attawut Chaibunruang
Goonnapa Fucharoen
Supan Fucharoen
2012
156. THALASSEMIA AND IRON DEFICIENCY IN RELATION TO ANEMIA AND MICROCYTOSIS AMONG NORTHEAST-THAI AND LAOTIAN PREGNANT WOMEN Jaruwan Tritipsombut
Kanokwan Sanchaisuriya
Prachatip Phollarp
Dalouny Bouakhasith
Pattara Sanchaisuriya
Goonnapa Fucharoen
Supan Fucharoen
Frank Schelp
2012
157. ALPHA-AND BETA-GLOBIN MRNA ANALYSIS: APPLICATION TO CHARACTERIZATION OF EIGHT HEMOGLOBIN VARIANTS FOUND IN THAILAND Kritsada Singha
Goonnapa Fucharoen
Supan Fucharoen
2013
158. AN UNUSUAL FORM OF THE AEBART'S DISEASE: MOLECULAR AND HEMATOLOGICAL CHARACTERISTICS Rossarin Karnpean
Attawut Chaibunruang
Goonnapa Fucharoen
Supan Fucharoen
2013
159. A proficiency testing program of hemoglobin analysis in prevention and control of severe hemoglobinopathies in Thailand. Karnpean, R.
Fucharoen, G.
Pansuwan, A.
Changtrakul, D.
Fucharoen, S.P.
2013
160. Association of Hb thailand [α56(E5)Lys→Thr] and Hb phnom penh [α117(GH5)-Ile-α118(H1)] with α;0-Thalassemia: Molecular and hematological features and differential diagnosis Singha, K
Srivorakun, H
Fucharoen, G
Changtrakul, Y
Komwilaisak, P
Jetsrisuparb, A
Puangplruk, R
Fucharoen, S
2013
161. ASSOCIATION OF Hb THAILAND [alpha 56(E5)Lys -> Thr] AND Hb PHNOM PENH [alpha 117(GH5)-Ile-alpha 118(H1)] WITH alpha(0)-THALASSEMIA: MOLECULAR AND HEMATOLOGICAL FEATURES AND DIFFERENTIAL DIAGNOSIS Kritsada Singha
Hataichanok Srivorakun
Goonnapa Fucharoen
Yossombat Changtrakul
Patcharee Komwilaisak
Arunee Jetsrisuparb
Rawiwan Puangplruk
Supan Fucharoen
2013
162. Burden of anemia in relation to thalassemia and iron deficiency among Vietnamese pregnant women. Siridamrongvattana, S.
Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, G.
Fucharoen, S.P.
Schelp, F.P.
2013
163. Fetal Red Blood Cell Parameters in Thalassemia and Hemoglobinopathies Karnpean, R
Fucharoen, G
Fucharoen, S
Ratanasiri, T
2013
164. FIVE HEMOGLOBIN VARIANTS IN A DOUBLE HETEROZYGOTE FOR ALPHA-AND BETA-GLOBIN CHAIN DEFECTS Supan Fucharoen
Kritsada Singha
Goonnapa Fucharoen
2013
165. Molecular and hematological characteristics of a novel form of α-globin gene triplication: The hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2 Singha, K
Fucharoen, G
Jetsrisuparb, A
Fucharoen, S
2013
166. Molecular and hematological characteristics of a novel form of alpha-globin gene triplication: The hemoglobin St.Luke's-Thailand [alpha 95(G2)Pro -> Arg] or Hb St. Luke's [A2] HBA2 Kritsada Singha
Goonnapa Fucharoen
Arunee Jetsrisuparb
Supan Fucharoen
2013
167. Molecular and hematological studies in a large cohort of α(0)-thalassemia in northeast Thailand: data from a single referral center. Attawut Chaibunruang
Simaporn Prommetta
Supawadee Yamsri
Goonnapa Fucharoen
Nattaya Sae-ung
Kanokwan Sanchaisuriya
Supan Fucharoen
2013
168. MOLECULAR BASES AND FREQUENCIES OF HEMOGLOBIN VARIANTS FOUND IN THAILAND: A RETROSPECTIVE DATA FROM A SINGLE REFERRAL CENTER IN NORTHEAST THAILAND Hataichanok Srivorakun
Kritsada Singha
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2013
169. No evidence for role of common anion exchanger 1 mutations on the severity difference in HB E-β-Thalassemia disease in Northeast Thailand Lalitpatch Ngouprommin
Nattaya Sae-ung
Supan Fucharoen
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Arunee Jetsrisuparb
2013
170. POSITIVE RATE OF THALASSEMIA IN NON-ANEMIC BLOOD SAMPLES WITH FLAGGING OF RED BLOOD CELL INDICES BY AUTOMATED CELL ANALYZER. Nattaya Sae-ung
Waraporn Chaichote
Wannisa Lhodsunthia
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2013
171. Prenatal and post-natal screening of β-thalassemia and hemoglobin E genes in Thailand using denaturing high performance liquid chromatography. Prajantasen, T.
Fucharoen, S.P.
Fucharoen, G.
Siriratmanawong, N.
2013
172. SECONDARY SCRENING OF ALPHA-THALASSEMIA 1USING A MODIFIED HB H INCLUSION BODY TEST Goonnapa Fucharoen
Khomsom Yooyen
Attawut Chaibunroung
Supan Fucharoen
2013
173. THALASSEMIA AND HEMOGLOBINOPATHIES IN THUA THIEN HUE PROVINCE, CENTRAL VIETNAM Nguyen, HV
Sanchaisuriya, K
Nguyen, D
Phan, HT
Siridamrongvattana, S
Sanchaisuriya, P
Fucharoen, S
Fucharoen, G
Schelp, FP
2013
174. A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration Srivorakun, H.
Singha, K.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2014
175. A newly modified hemoglobin h inclusion test as a secondary screening for α0-thalassemia in southeast asian populations Goonnapa Fucharoen
Khomsan Yooyen
Attawut Chaibunruang
Supan Fucharoen
2014
176. ARKRAY ADAMS A1c HA-8180T Analyzer for Diagnosis of Thalassemia and Hemoglobinopathies Common in Southeast Asia. Srivorakun, H.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2014
177. CONFIRMATION OF HB F ON AUTOMATED HEMOGLOBIN ANALYZER BY USING RAPID HB F TEST Goonnapa Fucharoen
Wachiraporn Taweenan
Supan Fucharoen
2014
178. DIFFERENTIATION OF HB E-DBO-THALASSEMIA AND HB E-BO-THALASSEMIA BY HB-ANALYSIS USING CAPILLARY ELECTROPHORESIS Supan Fucharoen
Nattaphol Prakobkaew
Goonnapa Fucharoen
2014
179. Five Hemoglobin Variants in a Double Heterozygote for alpha- and beta-Globin Chain Defects Singha, K
Fucharoen, G
Fucharoen, S
2014
180. Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis Ngouprommin, L
Sae-Ung, N
Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Jetsrisuparb, A
2014
181. Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand Chaibunruang, A
Karnpean, R
Fucharoen, G
Fucharoen, S
2014
182. GENOTYPE AND PHENOTYPE DIVERSITY OF THALASSEMIA AMONG POSITIVE-SCREENED LAOTIAN COUPLES Kasama Wongprachum
Kanokwan Sanchaisuriya
Maneelay Dethvongphanh
Boualay Norcharoen
Bousanit Htalongsengchan
Virak Vidamaly
Pattara Sanchaisuriya
Supan Fucharoen
Goonnapa Fucharoen
Frank P. Schelp
2014
183. HIGH HB F DETERMINANTS IN THAILAND: HEMATOLOGICAL AND MOLECULAR ANALYSIS Nattaphol Prakobkaew
Supan Fucharoen
Goonnapa Fucharoen
Nirut Siriratmanawong
2014
184. Interaction of hemoglobin Grey Lynn (Vientiane) with a non-deletional α(+)-thalassemia in an adult Thai proband. Kritsada Singha
Goonnapa Fucharoen
Supan Fucharoen
2014
185. Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: interaction of the β-globin erythroid Krüppel-like factor binding site mutation with Hb E and α(+)-thalassemia. Prajantasen, T
Teawtrakul, N
Fucharoen, G
Fucharoen, S
2014
186. Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: Interaction of the β-globin erythroid krüppel-like factor binding site mutation with Hb e and α+-thalassemia Prajantasen, T.
Teawtrakul, N.
Fucharoen, G.
Fucharoen, S.P.
2014
187. Molecular Characterization of a beta-Thalassemia Intermedia Patient Presenting Inferior Vena Cava Thrombosis: Interaction of the beta-Globin Erythroid Kruppel-Like Factor Binding Site Mutation with Hb E and alpha(+)-Thalassemia Thanet Prajantasen
Nattiya Teawtrakul
Goonnapa Fucharoen
Supan Fucharoen
2014
188. Red blood cell microparticles in hemoglobin E disorders Chaichote, W.
Sae-Ung, N.
Fucharoen, G.
Fucharoen, S.P.
2014
189. Routine screening for α-thalassaemia using an immunochromatographic strip assay for haemoglobin Bart's. Patcharawadee Prayalaw
Goonnapa Fucharoen
Supan Fucharoen
2014
190. Routine screening for a-thalassaemia using an immunochromatographic strip assay for haemoglobin bart’s Prayalaw, P.
Fucharoen, G.
Fucharoen, S.P.
2014
191. VALIDATION OF THE CUTOFF VALUES OF THE MEAN CORPUSCULAR VOLUME AND MEAN CORPUSCULAR HEMOGLOBIN ON FOUR AUTOMATED ANALYZERS FOR THALASSEMIA SCREENING Chaninthorn Chaitripop
Kanokwan Sanchaisuriya
Sakoun Inthavong
Supan Fucharoen
Goonnapa Fucharoen
Yossombut Changtrakul
Pattara Sanchaisuriya
2014
192. Variability of hemoglobin F expression in hemoglobin EE disease: Hematological and molecular analysis Naruwat Pakdee
Supawadee Yamsri
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Serge Pissard
Supan Fucharoen
2014
193. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations. Yamsri, S.
Singha, K.
Prajantasen, T.
Taweenan, W.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2015
194. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization. Singha, K
Fucharoen, G
Hama, A
Fucharoen, S
2015
195. A novel (A)gamma delta beta(0)-thalassemia caused by DNA deletion-inversion-insertion of the beta-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization Kritsada Singha
Goonnapa Fucharoen
Abdulloh Hama
Supan Fucharoen
2015
196. A novel Aγδβ0-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization Singha, K.
Fucharoen, G.
Hama, A.
Fucharoen, S.P.
2015
197. Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis Jomoui, W
Fucharoen, G
Sanchaisuriya, K
Nguyen, VH
Fucharoen, S
2015
198. High resolution melting analytical platform for rapid prenatal and postnatal diagnosis of beta-thalassemia common among Southeast Asian population Prajantasen, T.
Fucharoen, S.P.
Fucharoen, G.
2015
199. Interaction of Hb Grey Lynn (Vientiane) [alpha 91(FG3)Leu > Phe (alpha 1)] with Hb E [beta 26(B8) Glu > Lys] and alpha(+)-thalassemia: Molecular and Hematological Analysis Singha, K
Fucharoen, G
Fucharoen, S
2015
200. Interaction of Hb Grey Lynn (Vientiane) [α91(FG3)Leu>Phe (α1)] with Hb E [β26(B8) Glu>Lys] and α+-thalassemia: Molecular and hematological analysis Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2015
201. Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening. Panyasai, S.
Fucharoen, G.
Fucharoen, S.P.
2015
202. Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome. Tepakhan, W.
Yamsri, S.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2015
203. Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome Tepakhan, W.
Yamsri, S.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2015
204. Kruppel-like factor 1 mutations and expression of hemoglobins F and A(2) in homozygous hemoglobin E syndrome Wanicha Tepakhan
Supawadee Yamsri
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2015
205. Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women. Wongprachum, K.
Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, S.P.
Fucharoen, G.
Schelp, F.P.
2015
206. Red blood cell microparticles in hemoglobin E disorders. Chaichote, W.
Sae-Ung, N.
Fucharoen, G.
Fucharoen, S.P.
2015
207. Two Independent Genetic Origins of beta(+)-Thalassemia Due to-31 A to G Mutation in Thai and Japanese Populations Worrawalan Lerttham
Goonnapa Fucharoen
Supawadee Yamsri
Supan Fucharoen
2015
208. A MARKEDLY HIGH PROPORTION OF ALPHA-(0)-THALASSEMIA AND BETA-THALASSEMIA AMONG VIETNAMESE ETHNIC MINORITIES WITH MICROCYTOSIS: A COMMUNITY-BASED SURVEY IN NORTHERN VIETNAM Mai Anh Tuan
Kanokwan Sanchaisuriya
Nguyen Kieu Giang
Nguyen Tien Dung
Nguyen Van Son
Hoang Khai Lap
Pattara Sanchaisuriya
Supan Fucharoen
Goonnapa Fucharoen
2016
209. FLT3-ITD Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand. Fucharoen, G.
Sirijerachai, C.
Chainansamit, S.O.
Wiangnon, S.
2016
210. Hemoglobin Variants in Northern Thailand: Prevalence, Heterogeneity and Molecular Characteristics. Panyasai, S.
Fucharoen, G.
Fucharoen, S.P.
2016
211. INITIATION OF SCREENING PROGRAM FOR THALASSEMIA AT COMMUNITY LEVEL IN LAO PEOPLE'S DEMOCRATIC REPUBLIC: A GENOTYPE-PHENOTYPE DIVERSITY AMONG REPRODUCTIVE-AGE LAOTIAN WOMEN Konekeo Somphathabansouk
Kanokwan Sanchaisuriya
Virack Vidamaly
Pattara Sanchaisuriya
Supan Fucharoen
Goonnapa Fucharoen
2016
212. Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women Kasama Wongprachum
Kanokwan SanchaiSuriya
Maneelay Dethvongphanh
Boualay Norcharoen
Bousanit Htalongsengchan
Virack Vidarnaly
Pattara Sanchaisuriya
Supan Fucharoen
Goonnapa Fucharoen
Frank P. Schelp
2016
213. Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-beta-Thalassemia in Northeast Thailand Yamsri, S.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2016
214. Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder. Tepakhan, W.
Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2016
215. Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand Prayalaw, P.
Teawtrakul, N.
Jetsrisuparb, A.
Pongudom, S.
Fucharoen, G.
Fucharoen, S.P.
2016
216. PILOT SCREENING PROGRAM FOR THALASSEMIA IN A COUNTRY WITH LIMITED RESOURCES: A COLLABORATION MODEL BETWEEN CLOSE NEIGHBORING COUNTRIES Kasama Wongprachum
Kanokwan Sanchaisuriya
Virak Vidamaly
Souphathay Sorpasirth
Maneelay Dethvongphanh
Boualay Norcharoen
Bousanit Htalongsengchan
Goonnapa Fucharoen
Supan Fucharoen
Frank P. Schelp
Sastri Saowakontha
Pattara Sanchaisuriya
2016
217. Thalassemia Screening Using Different Automated Blood Cell Counters: Consideration of Appropriate Cutoff Values Sanchaisuriya, K.
Fucharoen, G.
Sanchaisuriya, P.
Changtrakun, Y.
Fucharoen, S.P.
2016
218. Co-inheritance of α(0) -thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications. K. Singha
H. Srivorakun
G. Fucharoen
S. Fucharoen
2017
219. Co-inheritance of α0-thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications Singha, K.
Srivorakun, H.
Fucharoen, G.
2017
220. DEVELOPMENT OF A PROFICIENCY TESTING PROGRAM FOR INITIAL THALASSEMIA SCREENING IN THAILAND Supan Fucharoen
Simaporn Prommetta
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Supawadee Yamsri
Attawut Chaibunruang
2017
221. Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system. H. Srivorakun
G. Fucharoen
K. Sanchaisuriya
S. Fucharoen
2017
222. DIFFERENTIATION OF HOMOZYGOUS HB E AND HOMOZYGOUS HB E WITH alpha(0)-THALASSEMIA BY MEANS OF HB A(2) LEVEL Kritsada Singha
Goonnapa Fucharoen
Supan Fucharoen
2017
223. DOUBLE CHECK PCR SYSTEMS FOR ACCURATE PRENATAL DIAGNOSIS OF HB BART & RSQUO; S HYDROPS FETALIS CAUSED BY (-(SEA)) & ALPHA;(0)-THALASSEMIA Wittaya Jomoui
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Patnaree Charoenwijitkul
Jitpanu Maneesarn
Supan Fucharoen
2017
224. Evaluation of staff performance and interpretation of the screening program for prevention of thalassemia Prommetta, S
Sanchaisuriya, K
Fucharoen, G
Yamsri, S
Chaiboonroeng, A
Fucharoen, S
2017
225. Genetic origin of alpha(0)-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome Jomoui, W
Fucharoen, G
Sanchaisuriya, K
Charoenwijitkul, P
Maneesarn, J
Xu, X
Fucharoen, S
2017
226. INITIATION OF APPROPRIATE SCREENING TESTS FOR SEVERE THALASSEMIA PREVENTION AT COMMUNITY LEVEL IN CAMBODIA Kimhaung Cheng
Arunee Jetsrisuparb
Supan Fucharoen
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Pattara Sanchaisuriya
2017
227. Molecular analysis of haemoglobin E in Southeast Asian populations Wittaya Jomoui
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Nga Thi Nguyen
Hoa Van Nguyen
Supan Fucharoen
2017
228. Novel interactions of two α-Hb variants with SEA deletion α(0)-thalassemia: hematological and molecular analyses. Srivorakun, H
Singha, K
Fucharoen, G
Fucharoen, S
2017
229. PILOT SCREENING PROGRAM FOR THALASSEMIA CARRIERS AT COMMUNITY LEVEL IN LAO PEOPLE'S DEMOCRATIC REPUBLIC Sanchaisuriya, K.
Fucharoen, S.P.
Fucharoen, G.
Schelp, F.P.
Sanchaisuriya, P.
2017
230. Screening of (-SEA) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies. Jomoui, W
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2017
231. Screening of (-(SEA)) alpha-thalassaemia using an immunochromatographic strip assay for the zeta-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies Wittaya Jomoui
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2017
232. Screening of (-SEA) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2017
233. Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups. Nga Thi Nguyen
Kanokwan Sanchaisuriya
Pattara Sanchaisuriya
Hoa Van Nguyen
Hoa Thi Thuy Phan
Goonnapa Fucharoen
Supan Fucharoen
2017
234. APPLICATION OF A NEW PORTABLE NEPHELOMETER FOR SCREENING THALASSEMIA IN COUNTRIES WITH LIMITED RESOURCES Jutatip Jamnok
Kanokwan Sanchaisuriya
Supawadee Yamsri
Goonnapa Fucharoen
Supan Fucharoen
Florian J. Schweigert
Pattara Sanchaisuriya
2018
235. Clinical Course of Homozygous Hemoglobin Constant Spring in Pediatric Patients Komvilaisak, P.
Jetsrisuparb, A.
Fucharoen, G.
Komwilaisak, R.
Jirapradittha, J.
Kiatchoosakun, P.
2018
236. EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin E-β0-thalassemia. Singha, K
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2018
237. EE score: An index for simple differentiation of homozygous hemoglobin e and hemoglobin E-β-thalassemia Singha, K.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2018
238. EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin -thalassemia Kritsada Singha
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2018
239. Effect of health education on severe thalassemia prevention and control in communities in Cambodia Fucharoen, S.P.
Sanchaisuriya, K.
Fucharoen, G.
Sanchaisuriya, P.
Jetsrisuparb, A.
2018
240. Elevations of Thrombotic Biomarkers in Hemoglobin H Disease Siriyakorn Chansai
Supan Fucharoen
Goonnapa Fucharoen
Arunee Jetsrisuparb
Worawan Chumpia
2018
241. Fetal anemia causing hydrops fetalis from an alpha-globin variant: Homozygous hemoglobin constant spring Komvilaisak, P.
Jetsrisuparb, A.
Wiangnon, S.
Jirapradittha, J.
Kiatchoosakun, P.
Fucharoen, G.
2018
242. Molecular Characteristics of Hb New York [113(G15)ValGlu, HBB: c.341T > A] in Thailand Attawut Chaibunruang
Kritsada Singha
Hataichanok Srivorakun
Goonnapa Fucharoen
Supan Fucharoen
2018
243. Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand. Chaibunruang, A
Singha, K
Srivorakun, H
Fucharoen, G
Fucharoen, S
2018
244. Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand Chaibunruang, A.
Singha, K.
Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
2018
245. Novel interactions of two alpha-Hb variants with SEA deletion alpha(0)-thalassemia: hematological and molecular analyses Hataichanok Srivorakun
Kritsada Singha
Goonnapa Fucharoen
Supan Fucharoen
2018
246. Novel interactions of two α-Hb variants with SEA deletion α0-thalassemia: hematological and molecular analyses Srivorakun, H.
Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2018
247. PHENOTYPIC EXPRESSION OF HB F, HB A(2) AND HB E IN THALASSEMIC AND NON-THALASSEMIC LAOTIAN CHILDREN AGED 6-24 MONTHS Benchawan Kingchaiyaphum
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Attawut Chaibunruang
Guy-Marino Hinnouho
Maxwell A. Barffour
Kimberly Ryan Wessells
Sonja Y. Hess
Sengchanh Kounnavong
Supan Fucharoen
2018
248. PRENATAL DIAGNOSIS OF SEVERE THALASSEMIA DISEASES USING DIRECT PCR ON AMNIOTIC FLUID SPECIMEN Phongsathorn Wichian
Supawadee Yamsri
Sudarat Kingpha
Suphatsak Phonamatarungrueang
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Supan Fucharoen
2018
249. Prevalence of thalassemia among newborns: A Re-visited after 20 Years of a Prevention and Control Program in Northeast Thailand Attawut Chaibunruang
Kanda Sornkayasit
Mattanee Chewasateanchai
Peerayoot Sanugul
Goonnapa Fucharoen
Supan Fucharoen
2018
250. RETICULOCYTE PARAMETERS IN THALASSEMIC AND NON-THALASSEMIC WOMEN OF REPRODUCTIVE AGE: APPLICABILITY TO PREDICTING IRON DEFICIENCY Jutatip Jamnok
Kanokwan Sanchaisuriya
Chaninthorn Chaitriphop
Pattara Sanchaisuriya
Goonnapa Fucharoen
Supan Fucharoen
2018
251. Whole Blood PCR for Rapid Screening of alpha(0)-Thalassemia Phongsathorn Wichian
Supawadee Yamsri
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Supan Fucharoen
2018
252. Whole blood PCR for rapid screening of α0-thalassemia Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2018
253. Whole Blood PCR for Rapid Screening of α-Thalassemia. Wichian, P
Yamsri, S
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2018
254. WHOLE BLOOD PCR KIT FOR RAPID IDENTIFICATION OF alpha(0)-THALASSEMIA Supawadee Yamsri
Phongsathorn Wichian
Rossarin Karnpean
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Supan Fucharoen
2018
255. Differentiation of homozygous hemoglobin E and hemoglobin E-(0)-thalassemia in children Areeda Arong
Greetapop Wangwok
Kritsada Singha
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Supan Fucharoen
2019
256. Differentiation of homozygous hemoglobin E and hemoglobin E-β 0 -thalassemia in children Singha, K.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2019
257. Differentiation of homozygous hemoglobin E and hemoglobin E-β -thalassemia in children. Arong, A
Wangwok, G
Singha, K
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2019
258. Dominant β-thalassaemia with unusually high Hb A2 and Hb F caused by βcD121(-G) (HBB:c.364delG) in exon 3 of β-globin gene Singha, K.
Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
2019
259. Erythrocyte indices in a large cohort of β-thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia Singha, K
Taweenan, W
Fucharoen, G
Fucharoen, S
2019
260. Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia Disease without α-Thalassemia. Yamsri, S.
Teawtrakul, N.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2019
261. Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G > A;92+7A > G]): a novel form of Hb E-beta-thalassaemia syndrome Singha, K
Fucharoen, G
Fucharoen, S
2019
262. Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G>A;92+7A>G]): A novel form of Hb E-β-thalassaemia syndrome Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2019
263. Molecular characteristics of alpha(+)-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics Thanyaornwanya Charoenwijitkul
Kritsada Singha
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Phuthita Thepphitak
Preawwalee Wintachai
Rossarin Karnpean
Supan Fucharoen
2019
264. Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics Singha, K.
Fucharoen, G.
Sanchaisuriya, K.
Karnpean, R.
Fucharoen, S.P.
2019
265. Molecular characteristics of α-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics. Charoenwijitkul, T
Singha, K
Fucharoen, G
Sanchaisuriya, K
Thepphitak, P
Wintachai, P
Karnpean, R
Fucharoen, S
2019
266. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia Srivorakun, H.
Chaibunruang, A.
Singha, K.
Tomanakarn, K.
Fucharoen, G.
Fucharoen, S.P.
2019
267. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α-Thalassemia. Pyae, AC
Srivorakun, H
Chaibunruang, A
Singha, K
Tomanakarn, K
Fucharoen, G
Fucharoen, S
2019
268. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of ?(+)-Thalassemia Aye Chan Pyae
Hataichanok Srivorakun
Attawut Chaibunruang
Kritsada Singha
Kanchana Tomanakarn
Goonnapa Fucharoen
Supan Fucharoen
2019
269. Presentation of Compound Heterozygous Hemoglobin Constant Spring and Hemoglobin Pakse in Neonates Komvilaisak, P
Jetsrisuparb, A
Fucharoen, G
Komwilaisak, R
Jirapradittha, J
Kiatchoosakun, P
2019
270. Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam Anh, TM
Sanchaisuriya, K
Kieu, GN
Tien, DN
Thu, HBT
Sanchaisuriya, P
Fucharoen, S
Fucharoen, G
Schelp, FP
2019
271. A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders Jomoui, W
Tepakhan, W
Yamsri, S
Srivorakun, H
Fucharoen, G
Fucharoen, S
2020
272. Factors associated with anaemia and iron deficiency among women of reproductive age in Northeast Thailand: a cross-sectional study Jamnok, J
Sanchaisuriya, K
Sanchaisuriya, P
Fucharoen, G
Fucharoen, S
Ahmed, F
2020
273. Hemoglobins F, A(2), and E levels in Laotian children aged 6-23 months with Hb E disorders: Effect of age, sex, and thalassemia types Benchawan Kingchaiyaphum
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Attawut Chaibunruang
Sonja Y. Hess
Guy-Marino Hinnouho
Maxwell A. Barffour
Kimbery R. Wessells
Sengchanh Kounnavong
Supan Fucharoen
2020
274. Hemoglobins F, A2, and E levels in Laotian children aged 6-23 months with Hb E disorders: Effect of age, sex, and thalassemia types Sanchaisuriya, K.
Fucharoen, G.
Chaibunruang, A.
Fucharoen, S.P.
2020
275. Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic. Singha, K.
Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
2020
276. Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects Singha, K.
Wiangnon, S.
Fucharoen, G.
Jetsrisuparb, A.
Komwilaisak, P.
Fucharoen, S.P.
2020
Count 168 157 178 1

Title Authors Year Publication name Cited count
< 2015 2016 2017 2018 2019 2020 Total
1. A novel ochre mutation in the β-thalassemia gene of a Thai. Identification by direct cloning of the entire β-globin gene amplified using polymerase chain reaction Fucharoen, G.
Fucharoen, P.
Fukumaki, Y.
1989 Journal of Biological Chemistry
14 (264), pp. 7780-7783
2. Heterogeneity of the γ-globin gene sequences in Japanese individuals: Implication of gene conversion in generation of polymorphisms Fucharoen, G.
Fukumaki, Y.
1989 Journal of Biochemistry
2 (105), pp. 184-189
3. Molecular basis of β-thalassemia in Thailand: analysis of β-thalassemia mutations using the polymerase chain reaction Fucharoen, G.
Laosombat, V.
Jetsrisuparb, A.
Tanphaichitr, V.S.
Suvatte, V.
Fukumaki, Y.
1989 Human Genetics
1 (84), pp. 41-46
4. A single nucleotide deletion in codon 123 of the β-globin gene causes an inclusion body β-thalassaemia trait: A novel elongated globin chain β(Makabe) Fucharoen, G.
Fukumaki, Y.
1990 British Journal of Haematology
3 (75), pp. 393-399
5. Molecular basis of HbE-β-thalassemia and the origin of HbE in northeast Thailand: Identification of one novel mutation using amplified DNA from buffy coat specimens Fucharoen, G.
Jetsrisuparb, A.
Fukumaki, Y.
1990 Biochemical and Biophysical Research Communications
2 (170), pp. 698-704
6. Molecular characterization and nonradioactive detection of beta-thalassemia in Malaysia Fucharoen, S.P.
Fucharoen, G.
Fukumaki, Y.
1990 Acta Haematologica
2 (84), pp. 82-88
7. Molecular heterogeneity of β-thalassaemia in the Japanese: Identification of two novel mutations Fucharoen, G.
Fukumaki, Y.
1990 British Journal of Haematology
1 (74), pp. 101-107
8. Simple non-radioactive method for detecting haemoglobin Constant Spring gene Fucharoen, S.P.
Fucharoen, G.
Fukumaki, Y.
1990 The Lancet
8704 (335), pp. 1527
9. Three-base deletion in exon 3 of the β-globin gene produced a novel variant (β gunma) with a thalassemia-like phenotype Fucharoen, G.
Fukumaki, Y.
1990 Blood
9 (76), pp. 1894-1896
10. Double heterozygosity of the β-Malay and a novel β-thalassemia gene in a Thai patient Fucharoen, S.P.
Fucharoen, G.
Laosombat, V.
Fukumaki, Y.
1991 American Journal of Hematology
2 (38), pp. 142-144
11. Eight-base deletion in exon 3 of the β-globin gene produced a novel variant (β Khon Kaen) with an inclusion body β-thalassemia trait [4] Fucharoen, G.
Fucharoen, S.P.
Jetsrisuparb, A.
Fukumaki, Y.
1991 Blood
2 (78), pp. 537-539
12. Molecular basis of beta thalassemia in the South of Thailand Laosombat, V.
Fucharoen, S.P.
Panich, V.
Fucharoen, G.
Nopparatana, C.
Fukumaki, Y.
1992 American Journal of Hematology
3 (41), pp. 194-198
13. Molecular heterogeneity of beta-thalassemia in Thailand. Fukumaki, Y.
Fucharoen, G.
Jetsrisuparb, A.
Nopparatana, C.
Laosombat, V.
Panich, V.
1992 The Southeast Asian journal of tropical medicine and public health
(23 Suppl 2), pp. 14-21
14. A simple non-radioactive assay for hemoglobin E gene in prenatal diagnosis Fucharoen, S.P.
Fucharoen, G.
Ratanasiri, T.
Jetsrisuparb, A.
Fukumaki, Y.
1994 Clinica Chimica Acta
1-2 (229), pp. 197-203
15. Rapid and simultaneous non-radioactive method for detecting α-thalassemia 1 (SEA type) and Hb Constant Spring genes Fucharoen, G.
Fucharoen, S.P.
1994 European Journal of Haematology
3 (53), pp. 186-187
16. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis. Fucharoen, S.P.
Fucharoen, G.
Ratanasiri, T.
Jetsrisuparb, A.
Fukumaki, Y.
1995 The Southeast Asian journal of tropical medicine and public health
(26 Suppl 1), pp. 278-281
17. Expression of hemoglobin E in newborn. Sae-Ung, N.
Fucharoen, G.
Fucharoen, S.P.
1995 The Southeast Asian journal of tropical medicine and public health
(26 Suppl 1), pp. 246-248
18. Molecular basis of alpha (0)-thalassemia in northeast of Thailand. Fucharoen, G.
Fucharoen, S.P.
Wanhakit, C.
Srithong, W.
1995 The Southeast Asian journal of tropical medicine and public health
(26 Suppl 1), pp. 249-251
19. mtDNA polymorphism in East Asian populations, with special reference to the peopling of Japan Hayasaka, K.
Fucharoen, G.
Park, K.
1996 American Journal of Human Genetics
3 (59), pp. 579-590
20. Beta-globin gene haplotypes in some minor ethnic groups in Thailand Fucharoen, G.
Fucharoen, S.P.
Chinoluck, P.
Khunsuk, S.
Sanchaisuriya, K.
Sae-Ung, N.
1997 Southeast Asian Journal of Tropical Medicine and Public Health
(28), pp. 115-119
21. Mitochondrial DNA polymorphism in East Asian populations with special reference to the peopling of Japan Fucharoen, G. 1997 Japanese Journal of Human Genetics
1 (42), pp. 51
22. Molecular and hematological characterization of HBE heterozygote with α-thalassemia determinant Sanchaisuriya, K.
Fucharoen, G.
Sae-Ung, N.
Sae-ue, N.
Baisungneon, R.
Jetsrisuparb, A.
Fucharoen, S.P.
1997 Southeast Asian Journal of Tropical Medicine and Public Health
(28), pp. 100-103
23. Molecular and hematological characterization of HB tak and HB pyrgos in Thailand Fucharoen, S.P.
Fucharoen, G.
Sae-Ung, N.
Sanchaisuriya, K.
Fukumaki, Y.
1997 Southeast Asian Journal of Tropical Medicine and Public Health
(28), pp. 110-114
24. Atypical hemoglobin H disease in a Thai patient resulting from a combination of α-thalassemia 1 and hemoglobin constant spring with hemoglobin J Bangkok heterozygosity Fucharoen, S.P.
Ayukarn, K.
Sanchaisuriya, K.
Fucharoen, G.
2001 European Journal of Haematology
5 (66), pp. 312-316
25. Mitochondrial DNA polymorphisms in Thailand Fucharoen, G.
Fucharoen, S.P.
2001 Journal of Human Genetics
3 (46), pp. 115-125
26. Molecular characterization of hemoglobin C in Thailand Sanchaisuriya, K.
Fucharoen, G.
Nattaya Sae-ung, N.
Siriratmanawong, I.
Surapot, S.
Fucharoen, S.P.
2001 American Journal of Hematology
3 (67), pp. 189-193
27. Molecular characterization of (δβ)°/β°-thalassemia and (δβ)°-thalassemia/hemoglobin E in Thai patients Fucharoen, S.P.
Pengjam, Y.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2001 European Journal of Haematology
4 (67), pp. 258-262
28. Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients [1] Fucharoen, S.P.
Sanchaisuriya, K.
Fucharoen, G.
Surapot, S.
2001 Haematologica
6 (86), pp. 657-658
29. Simultaneous PCR detection of β-thalassemia and α-thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome Siriratmanawong, N.
Fucharoen, G.
Sanchaisuriya, K.
Ratanasiri, T.
Fucharoen, S.P.
2001 Clinical Biochemistry
5 (34), pp. 377-380
30. A simplified screening for α-thalassemia 1 (SEA type) using a combination of a modified osmotic fragility test and a direct PCR on whole blood cell lysates Panyasai, S.
Sringam, P.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2002 Acta Haematologica
2 (108), pp. 74-78
31. Compound heterozygosity for Hb Korle-Bu (β73; Asp-Asn) and Hb E (β26; Glu-Lys) with a 3.7-kb deletional α-thalassemia in Thai patients Changtrakun, Y.
Fucharoen, S.P.
Ayukarn, K.
Siriratmanawong, N.
Fucharoen, G.
Sanchaisuriya, K.
2002 Annals of Hematology
7 (81), pp. 389-393
32. Frequency distribution and haplotypic heterogeneity of βE-globin gene among eight minority groups of northeast Thailand Fucharoen, G.
Fucharoen, S.P.
Sanchaisuriya, K.
Sae-Ung, N.
2002 Human Heredity
1 (53), pp. 18-22
33. Hb Paksé [(α2) codon 142 (TAA→TAT or Term→Tyr)] in Thai patients with EABart's disease and Hb H disease Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2002 Hemoglobin
3 (26), pp. 227-235
34. Molecular analysis of a Thai β-thalassaemia heterozygote with normal haemoglobin A2 level: Implication for population screening Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Pengjam, Y.
2002 Annals of Clinical Biochemistry
1 (39), pp. 44-49
35. Molecular and hematological characterization of HPFH-6/indian deletion-inversion Gγ(Aγδβ)O -Thalassemia and Gγ(Aγδβ)O -thalassemia/HbE in Thai patients Fucharoen, S.P.
Pengjam, Y.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2002 American Journal of Hematology
2 (71), pp. 109-113
36. Molecular characterization of Hb D-Punjab [β121(GH4)Glu → Gln] in Thailand Fucharoen, S.P.
Changtrakun, Y.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2002 Hemoglobin
3 (26), pp. 261-269
37. Molecular characterization of thalassemia intermedia associated with HPFH-6/β-thalassemia and HPFH-6/Hb E in Thai patients Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Surapot, S.
2002 Acta Haematologica
3 (108), pp. 157-161
38. Three major lineages of Asian Y chromosomes: Implications for the peopling of east and southeast Asia Tajima, A.
Fucharoen, G.
Fucharoen, S.P.
Tokunaga, K.
2002 Human Genetics
1 (110), pp. 80-88
39. Triple heterozygosity of a hemoglobin variant: Hemoglobin pyrgos with other hemoglobinopathies Jetsrisuparb, A.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
Wiangnon, S.
Komwilaisak, P.
2002 International Journal of Hematology
1 (75), pp. 35-39
40. Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family Fucharoen, S.P.
Changtrakun, Y.
Ratanasiri, T.
Fucharoen, G.
Sanchaisuriya, K.
2003 European Journal of Haematology
5 (70), pp. 304-309
41. Interaction of hemoglobin E and several forms of α-thalassemia in Cambodian families Fucharoen, S.P.
Sanchaisuriya, K.
Fucharoen, G.
Panyasai, S.
2003 Haematologica
10 (88), pp. 1092-1098
42. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of α-thalassemia in Thailand Sanchaisuriya, K.
Fucharoen, G.
Sae-Ung, N.
Jetsrisuparb, A.
Fucharoen, S.P.
2003 Annals of Hematology
10 (82), pp. 612-616
43. Non-invasive fetal sex determination using a conventional nested PCR analysis of fetal DNA in maternal plasma Tungwiwat, W.
Fucharoen, G.
Ratanasiri, T.
Sanchaisuriya, K.
Fucharoen, S.P.
2003 Clinica Chimica Acta
1-2 (334), pp. 173-177
44. Prenatal detection of fetal hemoglobin E gene from maternal plasma Fucharoen, G.
Tungwiwat, W.
Ratanasiri, T.
Sanchaisuriya, K.
Fucharoen, S.P.
2003 Prenatal Diagnosis
5 (23), pp. 393-396
45. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia Fucharoen, G.
Sanchaisuriya, K.
Sae-Ung, N.
Fucharoen, S.P.
2004 Bulletin of the World Health Organization
5 (82), pp. 364-372
46. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [α27(B8) Glu-Asp] and a deletional α-thalassaemia 2 in Thailand Chunpanich, S.
Ayukarn, K.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2004 Clinical and Laboratory Haematology
5 (26), pp. 355-358
47. Molecular and hematological characterization of hemoglobin hope/hemoglobin E and hemoglobin hope/α-Thalassemia 2 in Thai patients Chunpanich, S.
Fucharoen, S.P.
Sachaisuriya, K.
Fucharoen, G.
2004 Laboratory Hematology
4 (10), pp. 215-220
48. Molecular basis and hematologic characterization of δβ- thalassemia and hereditary persistence of fetal hemoglobin in Thailand Panyasai, S.
Fucharoen, S.P.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2004 Haematologica
7 (89), pp. 777-781
49. Multiplex allele-specific PCR assay for differential diagnosis of Hb S, Hb D-Punjab and Hb Tak Sanchaisuriya, K.
Chunpanich, S.
Fucharoen, G.
Fucharoen, S.P.
2004 Clinica Chimica Acta
1-2 (343), pp. 129-134
50. The diverse molecular basis and hematological features of Hb H and AEBart's diseases in northeast Thailand Boonsa, S.
Sanchaisuriya, K.
Fucharoen, G.
Wiangnon, S.
Jetsrisuparb, A.
Fucharoen, S.P.
2004 Acta Haematologica
3 (111), pp. 149-154
51. A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy: An alternative approach to electronic blood cell counting Sanchaisuriya, K.
Fucharoen, S.P.
Fucharoen, G.
Ratanasiri, T.
Sanchaisuriya, P.
Changtrakul, Y.
Ukosanakarn, U.
Schelp, F.P.
2005 American Journal of Clinical Pathology
1 (123), pp. 113-118
52. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy Sanchaisuriya, K.
Chunpanich, S.
Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, P.
Changtrakun, Y.
2005 European Journal of Haematology
3 (74), pp. 221-227
53. Compound heterozygote state for Gγ Aγ(δβ)°-thalassemia and hereditary persistence of fetal hemoglobin Fucharoen, S.P.
Panyasai, S.
Surapot, S.
Fucharoen, G.
Sanchaisuriya, K.
2005 American Journal of Hematology
2 (80), pp. 119-123
54. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: A molecular and hematological analysis Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Surapot, S.
2005 Blood Cells, Molecules, and Diseases
2 (35), pp. 196-200
55. Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients Fucharoen, S.P.
Singsanan, S.
Sanchaisuriya, K.
Fucharoen, G.
2005 Clinical and Laboratory Haematology
3 (27), pp. 184-189
56. Thalassemia intermedia associated with complex interaction of Hb Beijing [α16(A14)Lys→Asn] and Hb E [β26(B8)Glu→Lys] with a deletional α-thalassemia-1 in a Thai family Fucharoen, S.P.
Chunpanich, S.
Sanchaisuriya, K.
Fucharoen, G.
2005 Hemoglobin
1 (29), pp. 77-83
57. Development and application of a real-time quantitative PCR for prenatal detection of fetal α0-Thalassemia from maternal plasma Tungwiwat, W.
Fucharoen, S.P.
Fucharoen, G.
Ratanasiri, T.
Sanchaisuriya, K.
2006 Annals of the New York Academy of Sciences
(1075), pp. 103-107
58. Development of severe anemia during fever episodes in patients with hemoglobin E trait and hemoglobin H disease combinations Jetsrisuparb, A.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
Wiangnon, S.
Jetsrisuparb, C.
Sirijirachai, J.
Chansoong, K.
Chansung, G.
2006 Journal of Pediatric Hematology/Oncology
4 (28), pp. 249-253
59. Molecular and hematological profiles of hemoglobin EE disease with different forms of α-thalassemia Fucharoen, G.
Trithipsombat, J.
Sirithawee, S.
Yamsri, S.
Changtrakul, Y.
Sanchaisuriya, K.
Fucharoen, S.P.
2006 Annals of Hematology
7 (85), pp. 450-454
60. Thalassemia and hemoglobinopathies rather than iron deficiency are major causes of pregnancy-related anemia in northeast Thailand Sanchaisuriya, K.
Fucharoen, S.P.
Ratanasiri, T.
Sanchaisuriya, P.
Fucharoen, G.
Dietz, E.
Schelp, F.P.
2006 Blood Cells, Molecules, and Diseases
1 (37), pp. 8-11
61. α0-Thalassemia and related disorders in northeast Thailand: A molecular and hematological characterization Sae-Ung, N.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2007 Acta Haematologica
2 (117), pp. 78-82
62. Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-β-thalassemia Tungwiwat, W.
Fucharoen, G.
Fucharoen, S.P.
Ratanasiri, T.
Sanchaisuriya, K.
Sae-Ung, N.
2007 Translational Research
5 (150), pp. 319-325
63. Coexistence of Southeast Asian ovalocytosis and β-thalassemia: A molecular and hematological analysis Fucharoen, G.
Fucharoen, S.P.
Singsanan, S.
Sanchaisuriya, K.
2007 American Journal of Hematology
5 (82), pp. 381-385
64. Effect of the maternal βE-globin gene on hematologic responses to iron supplementation during pregnancy Sanchaisuriya, K.
Fucharoen, S.P.
Ratanasiri, T.
Sanchaisuriya, P.
Fucharoen, G.
Dietz, E.
Schelp, F.P.
2007 American Journal of Clinical Nutrition
2 (85), pp. 474-479
65. α/β-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function Kitcharoen, S.
Wilairat, P.
Jetsrisuparb, A.
Fucharoen, G.
Fucharoen, S.P.
2007 Clinical Biochemistry
18 (40), pp. 1373-1377
66. H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers Yamsri, S.
Sanchaisuriya, K.
Fucharoen, S.P.
Fucharoen, G.
Jetsrisuparb, A.
Wiangnon, S.
Changtrakul, Y.
Sanchaisuriya, P.
2007 Acta Haematologica
2 (118), pp. 99-105
67. Molecular characterization and origins of Hb constant spring and Hb Paksé in Southeast Asian populations Singsanan, S.
Fucharoen, G.
Savongsy, O.
Sanchaisuriya, K.
Fucharoen, S.P.
2007 Annals of Hematology
9 (86), pp. 665-669
68. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different αo-thalassemia determinants Siriratmanawong, N.
Fucharoen, G.
Fucharoen, S.P.
2007 Fetal Diagnosis and Therapy
4 (22), pp. 264-268
69. Rapid molecular characterization of Hb Queens and Hb Siam: Two variants easily misidentified as sickle Hb Fucharoen, S.P.
Singsanan, S.
Hama, A.
Fucharoen, G.
Sanchaisuriya, K.
2007 Clinical Biochemistry
1-2 (40), pp. 137-140
70. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: A molecular and hematological analysis Fucharoen, S.P.
Fucharoen, G.
Sae-Ung, N.
Sanchaisuriya, K.
2007 Blood Cells, Molecules, and Diseases
2 (39), pp. 195-198
71. Accuracy of fetal gender detection using a conventional nested PCR assay of maternal plasma in daily practice Tungwiwat, W.
Fucharoen, S.P.
Fucharoen, G.
Ratanasiri, T.
Sanchaisuriya, K.
2008 Australian and New Zealand Journal of Obstetrics and Gynaecology
5 (48), pp. 501-504
72. BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Sedgewick, A.E.
Timofeev, N.
Fucharoen, G.
Fucharoen, S.P.
Barbosa, C.G.
Vardarajan, B.N.
2008 Blood Cells, Molecules, and Diseases
3 (41), pp. 255-258
73. Effective screening for double heterozygosity of Hb E/α0 -thalassemia Sanchaisuriya, K.
Chirakul, S.
Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
Changtrakul, Y.
Sanchaisuriya, P.
2008 Annals of Hematology
11 (87), pp. 911-914
74. Hemoglobin profiles and hematologic features of thalassemic newborns: Application to screening of α-thalassemia 1 and hemoglobin E Tritipsombut, J.
Sanchaisuriya, K.
Fucharoen, S.P.
Fucharoen, G.
Siriratmanawong, N.
Sanchaisuriya, P.
2008 Archives of Pathology and Laboratory Medicine
11 (132), pp. 1739-1745
75. Thalassemia and hemoglobinopathies in pregnant Lao women: Carrier screening, prevalence and molecular basis Savongsy, O.
Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Sae-Ung, N.
2008 Annals of Hematology
8 (87), pp. 647-654
76. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
Sae-Ung, N.
Sanchaisuriya, K.
Ratanasiri, T.
2009 Acta Haematologica
4 (121), pp. 227-233
77. Analysis of fetal blood using capillary electrophoresis system: A simple method for prenatal diagnosis of severe thalassemia diseases Srivorakun, H.
Fucharoen, G.
Sae-Ung, N.
Sanchaisuriya, K.
Ratanasiri, T.
Fucharoen, S.P.
2009 European Journal of Haematology
1 (83), pp. 57-65
78. Complex interaction of Hb e [β26(B8)Glu→Lys], Hb Korle-Bu [β73(E17)Asp→Asn] and a deletional α-thalassemia-1 in pregnancy Siriratmanawong, N.
Chansri, W.
Singsanan, S.
Fucharoen, G.
Fucharoen, S.P.
2009 Hemoglobin
6 (33), pp. 507-514
79. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand Nuntakarn, L.
Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Jetsrisuparb, A.
Wiangnon, S.
2009 Blood Cells, Molecules, and Diseases
1 (42), pp. 32-35
80. Response to Dr. Dong-Zhi Li Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
Sae-Ung, N.
Sanchaisuriya, K.
Ratanasiri, T.
2009 Acta Haematologica
1 (122), pp. 51
81. Compound Heterozygous Hb TakHb e Causes Secondary Erythrocytosis in a Thai Family Teawtrakul, N.
Sirijirachai, C.
Chansung, G.
Chansung, G.
Fucharoen, G.
2010 Hemoglobin
2 (34), pp. 165-168
82. Hemoglobin Q-Thailand related disorders: Origin, molecular, hematological and diagnostic aspects Singsanan, S.
Karnpean, R.
Fucharoen, G.
Sanchaisuriya, K.
Sae-Ung, N.
Fucharoen, S.P.
2010 Blood Cells, Molecules, and Diseases
3 (45), pp. 210-214
83. Improvement of αo-thalassemia screening using combined osmotic fragility, dichlorophenolindophenol and Hb H inclusion tests Chaibunruang, A.
Pornphannukool, S.
Sae-Ung, N.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2010 Clinical Laboratory
3-4 (56), pp. 111-117
84. Interactions of hemoglobin Lepore (δβ hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis Chaibunruang, A.
Srivorakun, H.
Fucharoen, S.P.
Fucharoen, G.
Sae-Ung, N.
Sanchaisuriya, K.
2010 Blood Cells, Molecules, and Diseases
3 (44), pp. 140-145
85. Prevention of severe thalassemia in northeast Thailand: 16 Years of experience at a single university center Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Sae-Ung, N.
Ratanasiri, T.
Fucharoen, S.P.
2010 Prenatal Diagnosis
6 (30), pp. 540-546
86. Secondary erythrocytosis caused by hemoglobin Tak/(δβ)- thalassemia syndrome Prakobkaew, N.
Singsanan, S.
Fucharoen, G.
Surapot, S.
Fucharoen, S.P.
2010 Acta Haematologica
2 (124), pp. 115-119
87. Thalassemia and iron deficiency in a group of northeast Thai school children: Relationship to the occurrence of anemia Sanchaisuriya, K.
Yamsri, S.
Sanchaisuriya, P.
Fucharoen, G.
Fucharoen, S.P.
Schelp, F.P.
2010 European Journal of Pediatrics
11 (169), pp. 1317-1322
88. Anemia, iron deficiency and thalassemia among adolescents in Northeast Thailand: Results from two independent surveys Pansuwan, A.
Fucharoen, G.
Fucharoen, S.P.
2011 Acta Haematologica
4 (125), pp. 186-192
89. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α +-thalassemia Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
2011 European Journal of Haematology
1 (87), pp. 68-72
90. Evaluation of the URIT-2900 Automated Hematology Analyzer for screening of thalassemia and hemoglobinopathies in Southeast Asian populations Karnpean, R.
Pansuwan, A.
Fucharoen, G.
Fucharoen, S.P.
2011 Clinical Biochemistry
10-11 (44), pp. 889-893
91. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of β-thalassemia in northeast Thailand Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Sae-Ung, N.
Fucharoen, S.P.
2011 Blood Cells, Molecules, and Diseases
2 (47), pp. 120-124
92. Hb phimai [β72(E16)Ser→Thr]: A novel β-globin structural variant found in association with Hb constant spring in pregnancy Singsanan, S.
Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
2011 Hemoglobin
2 (35), pp. 103-110
93. Hemoglobin Lepore EF Bart's disease: A molecular, hematological, and diagnostic aspects Chaibunruang, A.
Fucharoen, G.
Jetsrisuparb, A.
Fucharoen, S.P.
2011 Annals of Hematology
11 (90), pp. 1337-1340
94. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system Fucharoen, G.
Srivorakun, H.
Singsanan, S.
Fucharoen, S.P.
2011 International Journal of Laboratory Hematology
4 (33), pp. 424-433
95. Thalassemia and hemoglobinopathies in Southeast Asian newborns: Diagnostic assessment using capillary electrophoresis system Srivorakun, H.
Fucharoen, G.
Changtrakul, Y.
Komwilaisak, P.
Fucharoen, S.P.
2011 Clinical Biochemistry
5-6 (44), pp. 406-411
96. A spurious haemoglobin A1c result associated with double heterozygote for haemoglobin Raleigh (β1[NA1]Val → Ala) and α+-thalassaemia Singha, K.
Fucharoen, G.
Chaibunruang, A.
Fucharoen, S.P.
2012 Annals of Clinical Biochemistry
5 (49), pp. 445-449
97. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals Chaibunruang, A.
Fucharoen, G.
Fucharoen, S.P.
2012 Hemoglobin
1 (36), pp. 80-84
98. Genetic origin and interaction of the Filipino β 0- thalassemia with Hb e and α-thalassemia in a Thai family Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2012 Translational Research
6 (159), pp. 473-476
99. Hb H disease with various β hemoglobinopathies: Molecular, hematological and diagnostic aspects Fucharoen, S.P.
Fucharoen, G.
2012 Hemoglobin
1 (36), pp. 18-24
100. Micromapping of thalassemia and hemoglobinopathies in diferent regions of Northeast Thailand and Vientaine, Laos People's Democratic Republic Tritipsombut, J.
Sanchaisuriya, K.
Phollarp, P.
Bouakhasith, D.
Sanchaisuriya, P.
Fucharoen, G.
Fucharoen, S.P.
Schelp, F.P.
2012 Hemoglobin
1 (36), pp. 47-56
101. Phenotypic expression of hemoglobins A2, E and F in various hemoglobin E related disorders Sae-Ung, N.
Srivorakun, H.
Fucharoen, G.
Yamsri, S.
Sanchaisuriya, K.
Fucharoen, S.P.
2012 Blood Cells, Molecules, and Diseases
1 (48), pp. 11-16
102. A proficiency testing program of hemoglobin analysis in prevention and control of severe hemoglobinopathies in Thailand Karnpean, R.
Fucharoen, G.
Pansuwan, A.
Changtrakul, D.
Fucharoen, S.P.
2013 Clinical Chemistry and Laboratory Medicine
6 (51), pp. 1265-1271
103. Association of Hb thailand [α56(E5)Lys→Thr] and Hb phnom penh [α117(GH5)-Ile-α118(H1)] with α;0-Thalassemia: Molecular and hematological features and differential diagnosis Singha, K.
Srivorakun, H.
Fucharoen, G.
Changtrakul, Y.
Komwilaisak, P.
Jetsrisuparb, A.
Fucharoen, S.P.
2013 Hemoglobin
1 (37), pp. 37-47
104. Burden of anemia in relation to thalassemia and iron deficiency among vietnamese pregnant women Siridamrongvattana, S.
Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, G.
Fucharoen, S.P.
Schelp, F.P.
2013 Acta Haematologica
4 (130), pp. 281-287
105. Fetal red blood cell parameters in thalassemia and hemoglobinopathies Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
Ratanasiri, T.
2013 Fetal Diagnosis and Therapy
3 (34), pp. 166-171
106. Molecular and hematological characteristics of a novel form of α-globin gene triplication: The hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2 Singha, K.
Fucharoen, G.
Jetsrisuparb, A.
Fucharoen, S.P.
2013 Clinical Biochemistry
7-8 (46), pp. 675-680
107. Molecular and hematological studies in a large cohort of α0-thalassemia in northeast Thailand: Data from a single referral center Chaibunruang, A.
Yamsri, S.
Fucharoen, G.
Sae-Ung, N.
Sanchaisuriya, K.
Fucharoen, S.P.
2013 Blood Cells, Molecules, and Diseases
2 (51), pp. 89-93
108. No evidence for role of common anion exchanger 1 mutations on the severity difference in HB E-β-Thalassemia disease in Northeast Thailand Ngouprommin, L.
Sae-Ung, N.
Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Jetsrisuparb, A.
2013 International Journal of Human Genetics
2 (13), pp. 99-103
109. Prenatal and post-natal screening of β-thalassemia and hemoglobin e genes in Thailand using denaturing high performance liquid chromatography Prajantasen, T.
Fucharoen, S.P.
Fucharoen, G.
Siriratmanawong, N.
2013 Molecular Biology Reports
4 (40), pp. 3173-3179
110. Thalassemia and Hemoglobinopathies in Thua Thien Hue Province, Central Vietnam Nguyen, H.V.
Sanchaisuriya, K.
Nguyen, D.H.
Siridamrongvattana, S.
Sanchaisuriya, P.
Fucharoen, S.P.
Fucharoen, G.
Schelp, F.P.
2013 Hemoglobin
4 (37), pp. 333-342
111. A large cohort of hemoglobin variants in thailand: Molecular epidemiological study and diagnostic consideration Srivorakun, H.
Singha, K.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2014 PLoS ONE
9 (9), pp.
112. A newly modified hemoglobin h inclusion test as a secondary screening for α0-thalassemia in southeast asian populations Fucharoen, G.
Yooyen, K.
Chaibunruang, A.
Fucharoen, S.P.
2014 Acta Haematologica
1 (132), pp. 10-14
113. ARKRAY ADAMS A1c HA-8180T analyzer for diagnosis of thalassemia and hemoglobinopathies common in southeast Asia Srivorakun, H.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2014 Laboratory Medicine
3 (45), pp. e112-e121
114. Five hemoglobin variants in a double heterozygote for α- and β-globin chain defects Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2014 Acta Haematologica
2 (131), pp. 71-75
115. Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: Prevalence and phenotypic analysis Ngouprommin, L.
Sae-Ung, N.
Fucharoen, S.P.
Fucharoen, G.
Sanchaisuriya, K.
Jetsrisuparb, A.
2014 Clinical Genetics
2 (85), pp. 198-200
116. Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand Chaibunruang, A.
Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
2014 Blood Cells, Molecules, and Diseases
4 (52), pp. 176-180
117. Interaction of hemoglobin Grey Lynn (Vientiane) with a non-deletional α+-thalassemia in an adult Thai proband Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2014 Biochemia Medica
1 (24), pp. 167-174
118. Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: Interaction of the β-globin erythroid krüppel-like factor binding site mutation with Hb e and α<sup>+</sup>-thalassemia Prajantasen, T.
Teawtrakul, N.
Fucharoen, G.
Fucharoen, S.P.
2014 Hemoglobin
6 (38), pp. 451-453
119. Red blood cell microparticles in hemoglobin E disorders Chaichote, W.
Sae-Ung, N.
Fucharoen, G.
Fucharoen, S.P.
2014 International Journal of Laboratory Hematology
(), pp.
120. Routine screening for a-thalassaemia using an immunochromatographic strip assay for haemoglobin bart’s Prayalaw, P.
Fucharoen, G.
Fucharoen, S.P.
2014 Journal of Medical Screening
3 (21), pp. 120-125
121. Variability of hemoglobin F expression in hemoglobin EE disease: Hematological and molecular analysis Yamsri, S.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2014 Blood Cells, Molecules, and Diseases
1-2 (53), pp. 11-15
122. A large cohort of β+-thalassemia in thailand: Molecular, hematological and diagnostic considerations Yamsri, S.
Singha, K.
Prajantasen, T.
Taweenan, W.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2015 Blood Cells, Molecules, and Diseases
2 (54), pp. 164-169
123. A novel <sup>A</sup>γδβ<sup>0</sup>-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization Singha, K.
Fucharoen, G.
Hama, A.
Fucharoen, S.P.
2015 Clinical Biochemistry
10-11 (48), pp. 703-708
124. High resolution melting analytical platform for rapid prenatal and postnatal diagnosis of β-thalassemia common among Southeast Asian population Prajantasen, T.
Fucharoen, S.P.
Fucharoen, G.
2015 Clinica Chimica Acta
(441), pp. 56-62
125. Interaction of Hb Grey Lynn (Vientiane) [α91(FG3)Leu>Phe (α1)] with Hb E [β26(B8) Glu>Lys] and α<sup>+</sup>-thalassemia: Molecular and hematological analysis Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2015 Clinical Laboratory
5-6 (61), pp. 631-635
126. Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening Panyasai, S.
Fucharoen, G.
Fucharoen, S.P.
2015 Clinica Chimica Acta
(438), pp. 226-230
127. Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome Tepakhan, W.
Yamsri, S.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2015 Annals of Hematology
(), pp.
128. Krüppel-like factor 1 mutations and expression of hemoglobins F and A<inf>2</inf> in homozygous hemoglobin E syndrome Tepakhan, W.
Yamsri, S.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2015 Annals of Hematology
7 (94), pp. 1093-1098
129. Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women Wongprachum, K.
Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, S.P.
Fucharoen, G.
Schelp, F.P.
2015 Acta Haematologica
(), pp. 65-69
130. Red blood cell microparticles in hemoglobin E disorders Chaichote, W.
Sae-Ung, N.
Fucharoen, G.
Fucharoen, S.P.
2015 International Journal of Laboratory Hematology
2 (37), pp. e52-e55
131. FLT3-ITD mutations in acute myeloid leukemia patients in northeast Thailand Fucharoen, G.
Sirijerachai, C.
Chainansamit, S.O.
Wiangnon, S.
2016 Asian Pacific Journal of Cancer Prevention
9 (17), pp. 4395-4399
132. Hemoglobin variants in Northern Thailand: Prevalence, heterogeneity and molecular characteristics Panyasai, S.
Fucharoen, G.
Fucharoen, S.P.
2016 Genetic Testing and Molecular Biomarkers
1 (20), pp. 37-43
133. Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women Wongprachum, K.
Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, S.P.
Fucharoen, G.
Schelp, F.P.
2016 Acta Haematologica
2 (135), pp. 65-69
134. Molecular understanding of non-transfusion-dependent thalassemia associated with hemoglobin E-β-thalassemia in northeast Thailand Yamsri, S.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2016 Acta Haematologica
4 (136), pp. 233-239
135. Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder Tepakhan, W.
Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2016 Blood Cells, Molecules, and Diseases
(59), pp. 85-91
136. Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand Prayalaw, P.
Teawtrakul, N.
Jetsrisuparb, A.
Pongudom, S.
Fucharoen, G.
Fucharoen, S.P.
2016 Acta haematologica
1 (135), pp. 15-20
137. Thalassemia screening using different automated blood cell counters: Consideration of appropriate cutoff values Sanchaisuriya, K.
Fucharoen, G.
Sanchaisuriya, P.
Changtrakun, Y.
Fucharoen, S.P.
2016 Clinical Laboratory
4 (62), pp. 545-552
138. Co-inheritance of α<sup>0</sup>-thalassemia elevates Hb A<inf>2</inf> level in homozygous Hb E: Diagnostic implications Singha, K.
Srivorakun, H.
Fucharoen, G.
2017 International Journal of Laboratory Hematology
5 (39), pp. 508-512
139. Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system Srivorakun, H.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2017 International Journal of Laboratory Hematology
1 (39), pp. 101-111
140. Evaluation of staff performance and interpretation of the screening program for prevention of thalassemia Sanchaisuriya, K.
Fucharoen, G.
Yamsri, S.
Fucharoen, S.P.
2017 Biochemia Medica
2 (27), pp. 387-397
141. Genetic origin of α 0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2017 Journal of Human Genetics
8 (62), pp. 747-754
142. Molecular analysis of haemoglobin E in Southeast Asian populations Fucharoen, G.
Sanchaisuriya, K.
Nguyen, H.V.
Fucharoen, S.P.
2017 Annals of Human Biology
8 (44), pp. 747-750
143. Pilot screening program for thalassemia carriers at community level in lao people’s democratic republic Sanchaisuriya, K.
Fucharoen, S.P.
Fucharoen, G.
Schelp, F.P.
Sanchaisuriya, P.
2017 Southeast Asian Journal of Tropical Medicine and Public Health
5 (48), pp. 1083-1092
144. Screening of (-<sup>SEA</sup>) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2017 Journal of Clinical Pathology
1 (70), pp. 63-68
145. Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, G.
Fucharoen, S.P.
2017 Journal of Community Genetics
3 (8), pp. 221-228
146. Clinical course of homozygous hemoglobin constant spring in pediatric patients Komvilaisak, P.
Jetsrisuparb, A.
Fucharoen, G.
Komwilaisak, R.
Jirapradittha, J.
Kiatchoosakun, P.
2018 Journal of Pediatric Hematology/Oncology
5 (40), pp. 409-412
147. EE score: An index for simple differentiation of homozygous hemoglobin e and hemoglobin E-β-thalassemia Singha, K.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2018 Clinical Chemistry and Laboratory Medicine
9 (56), pp. 1507-1513
148. Effect of health education on severe thalassemia prevention and control in communities in Cambodia Fucharoen, S.P.
Sanchaisuriya, K.
Fucharoen, G.
Sanchaisuriya, P.
Jetsrisuparb, A.
2018 Archives of Public Health
1 (76), pp.
149. Elevations of Thrombotic Biomarkers in Hemoglobin H Disease Fucharoen, S.P.
Fucharoen, G.
Jetsrisuparb, A.
Chumpia, W.
2018 Acta Haematologica
1 (139), pp. 47-51
150. Fetal anemia causing hydrops fetalis from an alpha-globin variant: Homozygous hemoglobin constant spring Komvilaisak, P.
Jetsrisuparb, A.
Wiangnon, S.
Jirapradittha, J.
Kiatchoosakun, P.
Fucharoen, G.
2018 Journal of Pediatric Hematology/Oncology
5 (40), pp. 405-408
151. Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T&gt;A] in Thailand Chaibunruang, A.
Singha, K.
Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
2018 Hemoglobin
1 (42), pp. 11-15
152. Novel interactions of two α-Hb variants with SEA deletion α<sup>0</sup>-thalassemia: hematological and molecular analyses Srivorakun, H.
Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2018 Hematology
3 (23), pp. 187-191
153. Prevalence of thalassemia among newborns: A Re-visited after 20 Years of a Prevention and Control Program in Northeast Thailand Chaibunruang, A.
Fucharoen, G.
Fucharoen, S.P.
2018 Mediterranean Journal of Hematology and Infectious Diseases
1 (10), pp.
154. Whole blood PCR for rapid screening of α<sup>0</sup>-thalassemia Yamsri, S.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2018 Annals of Clinical and Laboratory Science
2 (48), pp. 231-235
155. Differentiation of homozygous hemoglobin E and hemoglobin E-β <sup>0</sup> -thalassemia in children Singha, K.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2019 International Journal of Laboratory Hematology
3 (41), pp. e70-e72
156. Dominant β-thalassaemia with unusually high Hb A<inf>2</inf> and Hb F caused by β<sup>cD121(-G)</sup> (HBB:c.364delG) in exon 3 of β-globin gene Singha, K.
Karnpean, R.
Fucharoen, G.
Fucharoen, S.P.
2019 Journal of Clinical Pathology
(), pp.
157. Erythrocyte indices in a large cohort of β-thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2019 International Journal of Laboratory Hematology
4 (41), pp. 513-518
158. Molecular analysis of non-transfusion dependent thalassemia associated with hemoglobin E-β-Thalassemia disease without α-thalassemia Yamsri, S.
Teawtrakul, N.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2019 Mediterranean Journal of Hematology and Infectious Diseases
1 (11), pp.
159. Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G&gt;A;92+7A&gt;G]): A novel form of Hb E-β-thalassaemia syndrome Singha, K.
Fucharoen, G.
Fucharoen, S.P.
2019 Journal of Clinical Pathology
4 (72), pp. 322-324
160. Molecular characteristics of α<sup>+</sup>-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics Singha, K.
Fucharoen, G.
Sanchaisuriya, K.
Karnpean, R.
Fucharoen, S.P.
2019 Clinical Biochemistry
(71), pp. 31-37
161. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α<sup>+</sup>-Thalassemia Srivorakun, H.
Chaibunruang, A.
Singha, K.
Tomanakarn, K.
Fucharoen, G.
Fucharoen, S.P.
2019 Hemoglobin
4-5 (43), pp. 254-257
162. Presentation of Compound Heterozygous Hemoglobin Constant Spring and Hemoglobin Pakse in Neonates Komvilaisak, P.
Jetsrisuparb, A.
Fucharoen, G.
Komwilaisak, R.
Jirapradittha, J.
Kiatchoosakun, P.
2019 Journal of Pediatric Hematology/Oncology
6 (41), pp. E413-E415
163. Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, S.P.
Fucharoen, G.
Schelp, F.P.
2019 Hemoglobin
4-5 (43), pp. 249-253
164. A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders Tepakhan, W.
Yamsri, S.
Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
2020 Annals of Hematology
1 (99), pp. 23-29
165. Factors associated with anaemia and iron deficiency among women of reproductive age in Northeast Thailand: A cross-sectional study Sanchaisuriya, K.
Sanchaisuriya, P.
Fucharoen, G.
Fucharoen, S.P.
2020 BMC Public Health
1 (20), pp.
166. Hemoglobins F, A<inf>2</inf>, and E levels in Laotian children aged 6-23 months with Hb E disorders: Effect of age, sex, and thalassemia types Sanchaisuriya, K.
Fucharoen, G.
Chaibunruang, A.
Fucharoen, S.P.
2020 International Journal of Laboratory Hematology
(), pp.
167. Molecular basis of Hb H and AEBart’s diseases in the Lao People’s Democratic Republic Singha, K.
Srivorakun, H.
Fucharoen, G.
Fucharoen, S.P.
2020 International Journal of Laboratory Hematology
1 (42), pp. 23-27
168. Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects Singha, K.
Wiangnon, S.
Fucharoen, G.
Jetsrisuparb, A.
Komwilaisak, P.
Fucharoen, S.P.
2020 International Journal of Laboratory Hematology
(), pp.

Title Authors Year Journal title
1. Heterogeneity of the gamma-globin gene sequences in Japanese individuals: implication of gene conversion in generation of polymorphisms. Shiokawa, S
Fucharoen, S
Fucharoen, G
Tomatsu, S
Fukumaki, Y
1989 Journal of biochemistry
2 (105), pp. 184-9
2. A novel ochre mutation in the beta-thalassemia gene of a Thai. Identification by direct cloning of the entire beta-globin gene amplified using polymerase chain reactions. Fucharoen, S
Fucharoen, G
Fucharoen, P
Fukumaki, Y
1989 The Journal of biological chemistry
14 (264), pp. 7780-3
3. Molecular basis of beta-thalassemia in Thailand: analysis of beta-thalassemia mutations using the polymerase chain reaction. Fucharoen, S
Fucharoen, G
Sriroongrueng, W
Laosombat, V
Jetsrisuparb, A
Prasatkaew, S
Tanphaichitr, VS
Suvatte, V
Tuchinda, S
Fukumaki, Y
1989 Human genetics
1 (84), pp. 41-6
4. Molecular basis of HbE-beta-thalassemia and the origin of HbE in northeast Thailand: identification of one novel mutation using amplified DNA from buffy coat specimens. Fucharoen, G
Fucharoen, S
Jetsrisuparb, A
Fukumaki, Y
1990 Biochemical and biophysical research communications
2 (170), pp. 698-704
5. Molecular heterogeneity of beta-thalassaemia in the Japanese: identification of two novel mutations. Fucharoen, S
Katsube, T
Fucharoen, G
Sawada, H
Oishi, H
Katsuno, M
Nishimura, J
Motomura, S
Miura, Y
Fukumaki, Y
1990 British journal of haematology
1 (74), pp. 101-7
6. A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe. Fucharoen, S
Kobayashi, Y
Fucharoen, G
Ohba, Y
Miyazono, K
Fukumaki, Y
Takaku, F
1990 British journal of haematology
3 (75), pp. 393-9
7. Simple non-radioactive method for detecting haemoglobin Constant Spring gene. Fucharoen, S
Fucharoen, G
Fukumaki, Y
1990 Lancet (London, England)
8704 (335), pp. 1527
8. Molecular characterization and nonradioactive detection of beta-thalassemia in Malaysia. Fucharoen, S
Fucharoen, G
Ata, K
Aziz, S
Hashim, S
Hassan, K
Fukumaki, Y
1990 Acta haematologica
2 (84), pp. 82-8
9. Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype. Fucharoen, S
Fucharoen, G
Fukumaki, Y
Nakayama, Y
Hattori, Y
Yamamoto, K
Ohba, Y
1990 Blood
9 (76), pp. 1894-6
10. Double heterozygosity of the beta-Malay and a novel beta-thalassemia gene in a Thai patient. Fucharoen, S
Fucharoen, G
Laosombat, V
Fukumaki, Y
1991 American journal of hematology
2 (38), pp. 142-4
11. Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait. Fucharoen, G
Fuchareon, S
Jetsrisuparb, A
Fukumaki, Y
1991 Blood
2 (78), pp. 537-9
12. Molecular heterogeneity of beta-thalassemia in Thailand. Fukumaki, Y
Fucharoen, S
Fucharoen, G
Okamoto, N
Ichinose, M
Jetsrisuparb, A
Sriroongrueng, W
Nopparatana, C
Laosombat, V
Panich, V
1992 The Southeast Asian journal of tropical medicine and public health
(23), pp. 14-21
13. Molecular basis of beta thalassemia in the south of Thailand. Laosombat, V
Fucharoen, SP
Panich, V
Fucharoen, G
Wongchanchailert, M
Sriroongrueng, W
Nopparatana, C
Kenpitak, K
Maipang, M
Fukumaki, Y
1992 American journal of hematology
3 (41), pp. 194-8
14. Rapid and simultaneous non-radioactive method for detecting alpha-thalassemia 1 (SEA type) and Hb Constant Spring genes. Fucharoen, G
Fucharoen, S
1994 European journal of haematology
3 (53), pp. 186-7
15. A simple non-radioactive assay for hemoglobin E gene in prenatal diagnosis. Fucharoen, S
Fucharoen, G
Ratanasiri, T
Jetsrisuparb, A
Fukumaki, Y
1994 Clinica chimica acta; international journal of clinical chemistry
1 (229), pp. 197-203
16. Molecular basis of alpha (0)-thalassemia in northeast of Thailand. Fucharoen, G
Fucharoen, S
Wanhakit, C
Srithong, W
1995 The Southeast Asian journal of tropical medicine and public health
(26), pp. 249-51
17. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis. Fucharoen, S
Fucharoen, G
Ratanasiri, T
Jetsrisuparb, A
Fukumaki, Y
1995 The Southeast Asian journal of tropical medicine and public health
(26), pp. 278-81
18. Expression of hemoglobin E in newborn. Sae-ung, N
Fucharoen, G
Fucharoen, S
1995 The Southeast Asian journal of tropical medicine and public health
(26), pp. 246-8
19. mtDNA polymorphism in East Asian Populations, with special reference to the peopling of Japan. Horai, S
Murayama, K
Hayasaka, K
Matsubayashi, S
Hattori, Y
Fucharoen, G
Harihara, S
Park, KS
Omoto, K
Pan, IH
1996 American journal of human genetics
3 (59), pp. 579-90
20. Molecular and hematological characterization of Hb Tak and Hb Pyrgos in Thailand. Fucharoen, S
Fucharoen, G
Sae-ung, N
Sanchaisuriya, K
Fukumaki, Y
1997 The Southeast Asian journal of tropical medicine and public health
(28), pp. 110-4
21. Molecular and hematological characterization of HbE heterozygote with alpha-thalassemia determinant. Sanchaisuriya, K
Fucharoen, G
Sae-ung, N
Sae-ue, N
Baisungneon, R
Jetsrisuparb, A
Fucharoen, S
1997 The Southeast Asian journal of tropical medicine and public health
(28), pp. 100-3
22. Beta-globin gene haplotypes in some minor ethnic groups in Thailand. Fucharoen, G
Fucharoen, S
Wilai, Y
Chinoluck, P
Khunsuk, S
Sanchaisuriya, K
Sae-ung, N
1997 The Southeast Asian journal of tropical medicine and public health
(28), pp. 115-9
23. Molecular characterization of (deltabeta)(0)/beta(0)-thalassemia and (deltabeta)(0)-thalassemia/hemoglobin E in Thai patients. Fucharoen, S
Pengjam, Y
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2001 European journal of haematology
4 (67), pp. 258-62
24. Mitochondrial DNA polymorphisms in Thailand. Fucharoen, G
Fucharoen, S
Horai, S
2001 Journal of human genetics
3 (46), pp. 115-25
25. Simultaneous PCR detection of beta - thalassemia and alpha - thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome. Siriratmanawong, N
Fucharoen, G
Sanchaisuriya, K
Ratanasiri, T
Fucharoen, S
2001 Clinical biochemistry
5 (34), pp. 377-80
26. Atypical hemoglobin H disease in a Thai patient resulting from a combination of alpha-thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity. Fucharoen, S
Ayukarn, K
Sanchaisuriya, K
Fucharoen, G
2001 European journal of haematology
5 (66), pp. 312-6
27. Molecular characterization of hemoglobin C in Thailand. Sanchaisuriya, K
Fucharoen, G
Sae-ung, N
Siriratmanawong, N
Surapot, S
Fucharoen, S
2001 American journal of hematology
3 (67), pp. 189-93
28. Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients. Fucharoen, S
Sanchaisuriya, K
Fucharoen, G
Surapot, S
2001 Haematologica
6 (86), pp. 657-8
29. Molecular analysis of a thai beta-thalassaemia heterozygote with normal haemoglobin A2 level: implication for population screening. Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Pengjam, Y
2002 Annals of clinical biochemistry
0 (39), pp. 44-9
30. Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia. Tajima, A
Pan, IH
Fucharoen, G
Fucharoen, S
Matsuo, M
Tokunaga, K
Juji, T
Hayami, M
Omoto, K
Horai, S
2002 Human genetics
1 (110), pp. 80-8
31. Frequency Distribution and Haplotypic Heterogeneity of beta(E)-Globin Gene among Eight Minority Groups of Northeast Thailand. Fucharoen, G
Fucharoen, S
Sanchaisuriya, K
Sae-Ung, N
Suyasunanond, U
Sriwilai, P
Chinorak, P
2002 Human heredity
1 (53), pp. 18-22
32. Molecular characterization of thalassemia intermedia associated with HPFH-6/beta-thalassemia and HPFH-6/Hb E in Thai patients. Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Surapot, S
2002 Acta haematologica
3 (108), pp. 157-61
33. Hb Paksé [(alpha2) codon 142 (TAA-->TAT or Term-->Tyr)J in Thai patients with EAbart's disease and Hb H Disease. Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2002 Hemoglobin
3 (26), pp. 227-35
34. Molecular characterization of Hb D-Punjab [beta121(GH4)Glu-->Gln] in Thailand. Fucharoen, S
Changtrakun, Y
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2002 Hemoglobin
3 (26), pp. 261-9
35. Triple heterozygosity of a hemoglobin variant: hemoglobin Pyrgos with other hemoglobinopathies. Jetsrisuparb, A
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
Wiangnon, S
Komwilaisak, P
2002 International journal of hematology
1 (75), pp. 35-9
36. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients. Changtrakun, Y
Fucharoen, S
Ayukarn, K
Siriratmanawong, N
Fucharoen, G
Sanchaisuriya, K
2002 Annals of hematology
7 (81), pp. 389-93
37. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients. Fucharoen, S
Pengjam, Y
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2002 American journal of hematology
2 (71), pp. 109-13
38. Prenatal detection of fetal hemoglobin E gene from maternal plasma. Fucharoen, G
Tungwiwat, W
Ratanasiri, T
Sanchaisuriya, K
Fucharoen, S
2003 Prenatal diagnosis
5 (23), pp. 393-6
39. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family. Fucharoen, S
Changtrakun, Y
Ratanasiri, T
Fucharoen, G
Sanchaisuriya, K
2003 European journal of haematology
5 (70), pp. 304-9
40. Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families. Fucharoen, S
Sanchaisuriya, K
Fucharoen, G
Panyasai, S
Devenish, R
Luy, L
2003 Haematologica
10 (88), pp. 1092-8
41. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand. Sanchaisuriya, K
Fucharoen, G
Sae-ung, N
Jetsrisuparb, A
Fucharoen, S
2003 Annals of hematology
10 (82), pp. 612-6
42. Non-invasive fetal sex determination using a conventional nested PCR analysis of fetal DNA in maternal plasma. Tungwiwat, W
Fucharoen, G
Ratanasiri, T
Sanchaisuriya, K
Fucharoen, S
2003 Clinica chimica acta; international journal of clinical chemistry
1 (334), pp. 173-7
43. Molecular and hematological characterization of hemoglobin Hope/hemoglobin E and hemoglobin Hope/alpha-thalassemia 2 in Thai patients. Chunpanich, S
Fucharoen, S
Sanchaisuriya, K
Fucharoen, G
Kam-itsara, K
2004 Laboratory hematology : official publication of the International Society for Laboratory Hematology
4 (10), pp. 215-20
44. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand. Panyasai, S
Fucharoen, S
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2004 Haematologica
7 (89), pp. 777-81
45. The diverse molecular basis and hematological features of Hb H and AEBart's diseases in Northeast Thailand. Boonsa, S
Sanchaisuriya, K
Fucharoen, G
Wiangnon, S
Jetsrisuparb, A
Fucharoen, S
2004 Acta haematologica
3 (111), pp. 149-54
46. Multiplex allele-specific PCR assay for differential diagnosis of Hb S, Hb D-Punjab and Hb Tak. Sanchaisuriya, K
Chunpanich, S
Fucharoen, G
Fucharoen, S
2004 Clinica chimica acta; international journal of clinical chemistry
1 (343), pp. 129-34
47. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia. Fucharoen, G
Sanchaisuriya, K
Sae-ung, N
Dangwibul, S
Fucharoen, S
2004 Bulletin of the World Health Organization
5 (82), pp. 364-72
48. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand. Chunpanich, S
Ayukarn, K
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2004 Clinical and laboratory haematology
5 (26), pp. 355-8
49. Compound heterozygote state for GgammaAgamma(deltabeta) degrees -thalassemia and hereditary persistence of fetal hemoglobin. Fucharoen, S
Panyasai, S
Surapot, S
Fucharoen, G
Sanchaisuriya, K
2005 American journal of hematology
2 (80), pp. 119-23
50. A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy: an alternative approach to electronic blood cell counting. Sanchaisuriya, K
Fucharoen, S
Fucharoen, G
Ratanasiri, T
Sanchaisuriya, P
Changtrakul, Y
Ukosanakarn, U
Ussawaphark, W
Schelp, FP
2005 American journal of clinical pathology
1 (123), pp. 113-8
51. Thalassemia intermedia associated with complex interaction of Hb Beijing [alpha16(A14)Lys-->Asn] and Hb E [beta26(B8)Glu-->Lys] with a deletional alpha-thalassemia-1 in a Thai family. Fucharoen, S
Chunpanich, S
Sanchaisuriya, K
Fucharoen, G
Kunyanone, N
2005 Hemoglobin
1 (29), pp. 77-83
52. Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients. Fucharoen, S
Singsanan, S
Sanchaisuriya, K
Fucharoen, G
2005 Clinical and laboratory haematology
3 (27), pp. 184-9
53. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy. Sanchaisuriya, K
Chunpanich, S
Fucharoen, S
Fucharoen, G
Sanchaisuriya, P
Changtrakun, Y
2005 European journal of haematology
3 (74), pp. 221-7
54. Molecular and hematological profiles of hemoglobin EE disease with different forms of alpha-thalassemia. Fucharoen, G
Trithipsombat, J
Sirithawee, S
Yamsri, S
Changtrakul, Y
Sanchaisuriya, K
Fucharoen, S
2006 Annals of hematology
7 (85), pp. 450-4
55. Development of severe anemia during fever episodes in patients with hemoglobin E trait and hemoglobin H disease combinations. Jetsrisuparb, A
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
Wiangnon, S
Jetsrisuparb, C
Sirijirachai, J
Chansoong, K
2006 Journal of pediatric hematology/oncology
4 (28), pp. 249-53
56. Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma. Tungwiwat, W
Fucharoen, S
Fucharoen, G
Ratanasiri, T
Sanchaisuriya, K
2006 Annals of the New York Academy of Sciences
(1075), pp. 103-7
57. Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations. Singsanan, S
Fucharoen, G
Savongsy, O
Sanchaisuriya, K
Fucharoen, S
2007 Annals of hematology
9 (86), pp. 665-9
58. Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia. Tungwiwat, W
Fucharoen, G
Fucharoen, S
Ratanasiri, T
Sanchaisuriya, K
Sae-Ung, N
2007 Translational research : the journal of laboratory and clinical medicine
5 (150), pp. 319-25
59. Effect of the maternal betaE-globin gene on hematologic responses to iron supplementation during pregnancy. Sanchaisuriya, K
Fucharoen, S
Ratanasiri, T
Sanchaisuriya, P
Fucharoen, G
Dietz, E
Schelp, FP
2007 The American journal of clinical nutrition
2 (85), pp. 474-9
60. Coexistence of Southeast Asian ovalocytosis and beta-thalassemia: a molecular and hematological analysis. Fucharoen, G
Fucharoen, S
Singsanan, S
Sanchaisuriya, K
2007 American journal of hematology
5 (82), pp. 381-5
61. Rapid molecular characterization of Hb Queens and Hb Siam: two variants easily misidentified as sickle Hb. Fucharoen, S
Singsanan, S
Hama, A
Fucharoen, G
Sanchaisuriya, K
2007 Clinical biochemistry
1 (40), pp. 137-40
62. Alpha(0)-thalassemia and related disorders in northeast Thailand: a molecular and hematological characterization. Sae-ung, N
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2007 Acta haematologica
2 (117), pp. 78-82
63. alpha/beta-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function. Chaisue, C
Kitcharoen, S
Wilairat, P
Jetsrisuparb, A
Fucharoen, G
Fucharoen, S
2007 Clinical biochemistry
18 (40), pp. 1373-7
64. H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers. Yamsri, S
Sanchaisuriya, K
Fucharoen, S
Fucharoen, G
Jetsrisuparb, A
Wiangnon, S
Changtrakul, Y
Sanchaisuriya, P
2007 Acta haematologica
2 (118), pp. 99-105
65. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants. Siriratmanawong, N
Pinmuang-Ngam, C
Fucharoen, G
Fucharoen, S
2007 Fetal diagnosis and therapy
4 (22), pp. 264-8
66. Thalassemia and hemoglobinopathies in pregnant Lao women: carrier screening, prevalence and molecular basis. Savongsy, O
Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Sae-Ung, N
2008 Annals of hematology
8 (87), pp. 647-54
67. Accuracy of fetal gender detection using a conventional nested PCR assay of maternal plasma in daily practice. Tungwiwat, W
Fucharoen, S
Fucharoen, G
Ratanasiri, T
Sanchaisuriya, K
2008 The Australian & New Zealand journal of obstetrics & gynaecology
5 (48), pp. 501-4
68. Hemoglobin profiles and hematologic features of thalassemic newborns: application to screening of alpha-thalassemia 1 and hemoglobin E. Tritipsombut, J
Sanchaisuriya, K
Fucharoen, S
Fucharoen, G
Siriratmanawong, N
Pinmuang-ngam, C
Sanchaisuriya, P
2008 Archives of pathology & laboratory medicine
11 (132), pp. 1739-45
69. Effective screening for double heterozygosity of Hb E/alpha0-thalassemia. Sanchaisuriya, K
Chirakul, S
Srivorakun, H
Fucharoen, G
Fucharoen, S
Changtrakul, Y
Sanchaisuriya, P
2008 Annals of hematology
11 (87), pp. 911-4
70. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases. Srivorakun, H
Fucharoen, G
Sae-Ung, N
Sanchaisuriya, K
Ratanasiri, T
Fucharoen, S
2009 European journal of haematology
1 (83), pp. 57-65
71. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system. Karnpean, R
Fucharoen, G
Fucharoen, S
Sae-ung, N
Sanchaisuriya, K
Ratanasiri, T
2009 Acta haematologica
4 (121), pp. 227-33
72. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy. Siriratmanawong, N
Chansri, W
Singsanan, S
Fucharoen, G
Fucharoen, S
2009 Hemoglobin
6 (33), pp. 507-14
73. Interactions of hemoglobin Lepore (deltabeta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis. Chaibunruang, A
Srivorakun, H
Fucharoen, S
Fucharoen, G
Sae-ung, N
Sanchaisuriya, K
2010 Blood cells, molecules & diseases
3 (44), pp. 140-5
74. Improvement of alpha(0)-thalassemia screening using combined osmotic fragility, dichlorophenolindophenol and Hb H inclusion tests. Chaibunruang, A
Pornphannukool, S
Sae-Ung, N
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2010 Clinical laboratory
3 (56), pp. 111-7
75. Secondary erythrocytosis caused by hemoglobin Tak/(δβ)0-thalassemia syndrome. Prakobkaew, N
Singsanan, S
Fucharoen, G
Surapot, S
Fucharoen, S
2010 Acta haematologica
2 (124), pp. 115-9
76. Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects. Singsanan, S
Karnpean, R
Fucharoen, G
Sanchaisuriya, K
Sae-Ung, N
Fucharoen, S
2010 Blood cells, molecules & diseases
3 (45), pp. 210-4
77. Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center. Yamsri, S
Sanchaisuriya, K
Fucharoen, G
Sae-Ung, N
Ratanasiri, T
Fucharoen, S
2010 Prenatal diagnosis
6 (30), pp. 540-6
78. Thalassemia and iron deficiency in a group of northeast Thai school children: relationship to the occurrence of anemia. Panomai, N
Sanchaisuriya, K
Yamsri, S
Sanchaisuriya, P
Fucharoen, G
Fucharoen, S
Schelp, FP
2010 European journal of pediatrics
11 (169), pp. 1317-22
79. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family. Teawtrakul, N
Sirijirachai, C
Chansung, G
Fucharoen, G
2010 Hemoglobin
2 (34), pp. 165-8
80. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand. Yamsri, S
Sanchaisuriya, K
Fucharoen, G
Sae-Ung, N
Fucharoen, S
2011 Blood cells, molecules & diseases
2 (47), pp. 120-4
81. Evaluation of the URIT-2900 automated hematology analyzer for screening of thalassemia and hemoglobinopathies in Southeast Asian populations. Karnpean, R
Pansuwan, A
Fucharoen, G
Fucharoen, S
2011 Clinical biochemistry
10 (44), pp. 889-93
82. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia. Srivorakun, H
Fucharoen, G
Puangplruk, R
Kheawon, N
Fucharoen, S
2011 European journal of haematology
1 (87), pp. 68-72
83. Hb Phimai [β72(E16)Ser→Thr]: a novel β-globin structural variant found in association with Hb constant spring in pregnancy. Singsanan, S
Srivorakun, H
Fucharoen, G
Puangplruk, R
Fucharoen, S
2011 Hemoglobin
2 (35), pp. 103-10
84. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system. Fucharoen, G
Srivorakun, H
Singsanan, S
Fucharoen, S
2011 International journal of laboratory hematology
4 (33), pp. 424-33
85. Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects. Chaibunruang, A
Fucharoen, G
Jetsrisuparb, A
Fucharoen, S
2011 Annals of hematology
11 (90), pp. 1337-40
86. Thalassemia and hemoglobinopathies in Southeast Asian newborns: diagnostic assessment using capillary electrophoresis system. Srivorakun, H
Fucharoen, G
Changtrakul, Y
Komwilaisak, P
Fucharoen, S
2011 Clinical biochemistry
5 (44), pp. 406-11
87. Anemia, iron deficiency and thalassemia among adolescents in Northeast Thailand: results from two independent surveys. Pansuwan, A
Fucharoen, G
Fucharoen, S
Himakhun, B
Dangwiboon, S
2011 Acta haematologica
4 (125), pp. 186-92
88. A spurious haemoglobin A(1c) result associated with double heterozygote for haemoglobin Raleigh (β1[NA1]Val → Ala) and α(+)-thalassaemia. Singha, K
Fucharoen, G
Chaibunruang, A
Netnee, P
Fucharoen, S
2012 Annals of clinical biochemistry
0 (49), pp. 445-9
89. Genetic origin and interaction of the Filipino β⁰-thalassemia with Hb E and α-thalassemia in a Thai family. Yamsri, S
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2012 Translational research : the journal of laboratory and clinical medicine
6 (159), pp. 473-6
90. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects. Fucharoen, S
Fucharoen, G
2012 Hemoglobin
1 (36), pp. 18-24
91. Micromapping of thalassemia and hemoglobinopathies in diferent regions of northeast Thailand and Vientiane, Laos People's Democratic Republic. Tritipsombut, J
Sanchaisuriya, K
Phollarp, P
Bouakhasith, D
Sanchaisuriya, P
Fucharoen, G
Fucharoen, S
Schelp, FP
2012 Hemoglobin
1 (36), pp. 47-56
92. Phenotypic expression of hemoglobins A₂, E and F in various hemoglobin E related disorders. Sae-ung, N
Srivorakun, H
Fucharoen, G
Yamsri, S
Sanchaisuriya, K
Fucharoen, S
2012 Blood cells, molecules & diseases
1 (48), pp. 11-6
93. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals. Chaibunruang, A
Fucharoen, G
Fucharoen, S
2012 Hemoglobin
1 (36), pp. 80-4
94. Thalassemia and hemoglobinopathies in Thua Thien Hue Province, Central Vietnam. Nguyen, HV
Sanchaisuriya, K
Nguyen, D
Phan, HT
Siridamrongvattana, S
Sanchaisuriya, P
Fucharoen, S
Fucharoen, G
Schelp, FP
2013 Hemoglobin
4 (37), pp. 333-42
95. Prenatal and post-natal screening of β-thalassemia and hemoglobin E genes in Thailand using denaturing high performance liquid chromatography. Prajantasen, T
Fucharoen, S
Fucharoen, G
Siriratmanawong, N
Pinmuang-Ngam, C
2013 Molecular biology reports
4 (40), pp. 3173-9
96. A proficiency testing program of hemoglobin analysis in prevention and control of severe hemoglobinopathies in Thailand. Karnpean, R
Fucharoen, G
Pansuwan, A
Changtrakul, D
Fucharoen, S
2013 Clinical chemistry and laboratory medicine : CCLM / FESCC
6 (51), pp. 1265-71
97. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α(0)-thalassemia: molecular and hematological features and differential diagnosis. Singha, K
Srivorakun, H
Fucharoen, G
Changtrakul, Y
Komwilaisak, P
Jetsrisuparb, A
Puangplruk, R
Fucharoen, S
2013 Hemoglobin
1 (37), pp. 37-47
98. Fetal red blood cell parameters in thalassemia and hemoglobinopathies. Karnpean, R
Fucharoen, G
Fucharoen, S
Ratanasiri, T
2013 Fetal diagnosis and therapy
3 (34), pp. 166-71
99. Molecular and hematological studies in a large cohort of α(0)-thalassemia in northeast Thailand: data from a single referral center. Chaibunruang, A
Prommetta, S
Yamsri, S
Fucharoen, G
Sae-Ung, N
Sanchaisuriya, K
Fucharoen, S
2013 Blood cells, molecules & diseases
2 (51), pp. 89-93
100. Burden of anemia in relation to thalassemia and iron deficiency among Vietnamese pregnant women. Siridamrongvattana, S
Van Hoa, N
Sanchaisuriya, K
Dung, N
Hoa, PT
Sanchaisuriya, P
Fucharoen, G
Fucharoen, S
Schelp, FP
2013 Acta haematologica
4 (130), pp. 281-7
101. Molecular and hematological characteristics of a novel form of α-globin gene triplication: the hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2. Singha, K
Fucharoen, G
Jetsrisuparb, A
Fucharoen, S
2013 Clinical biochemistry
7 (46), pp. 675-80
102. Genetic heterogeneity of hemoglobin AEBart's disease: a large cohort data from a single referral center in northeast Thailand. Chaibunruang, A
Karnpean, R
Fucharoen, G
Fucharoen, S
2014 Blood cells, molecules & diseases
4 (52), pp. 176-80
103. Routine screening for α-thalassaemia using an immunochromatographic strip assay for haemoglobin Bart's. Prayalaw, P
Fucharoen, G
Fucharoen, S
2014 Journal of medical screening
3 (21), pp. 120-5
104. Interaction of hemoglobin Grey Lynn (Vientiane) with a non-deletional α(+)-thalassemia in an adult Thai proband. Singha, K
Fucharoen, G
Fucharoen, S
2014 Biochemia medica
1 (24), pp. 167-74
105. ARKRAY ADAMS A1c HA-8180T Analyzer for Diagnosis of Thalassemia and Hemoglobinopathies Common in Southeast Asia. Kunwandee, J
Srivorakun, H
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2014 Laboratory medicine
3 (45), pp. e112-21
106. A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration. Srivorakun, H
Singha, K
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2014 PloS one
9 (9), pp. e108365
107. Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: interaction of the β-globin erythroid Krüppel-like factor binding site mutation with Hb E and α(+)-thalassemia. Prajantasen, T
Teawtrakul, N
Fucharoen, G
Fucharoen, S
2014 Hemoglobin
6 (38), pp. 451-3
108. Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis. Ngouprommin, L
Sae-Ung, N
Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Jetsrisuparb, A
2014 Clinical genetics
2 (85), pp. 198-200
109. A newly modified hemoglobin H inclusion test as a secondary screening for α(0)-thalassemia in Southeast Asian populations. Fucharoen, G
Yooyen, K
Chaibunruang, A
Fucharoen, S
2014 Acta haematologica
1 (132), pp. 10-4
110. Five hemoglobin variants in a double heterozygote for α- and β-globin chain defects. Singha, K
Fucharoen, G
Fucharoen, S
2014 Acta haematologica
2 (131), pp. 71-5
111. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations. Yamsri, S
Singha, K
Prajantasen, T
Taweenan, W
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2015 Blood cells, molecules & diseases
2 (54), pp. 164-9
112. Interaction of Hb Grey Lynn (Vientiane) [α91(FG3)Leu>Phe (α1)] with Hb E [β26(B8) Glu>Lys] and α(+)-thalassemia: Molecular and Hematological Analysis. Singha, K
Fucharoen, G
Fucharoen, S
2015 Clinical laboratory
5 (61), pp. 631-5
113. Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis. Jomoui, W
Fucharoen, G
Sanchaisuriya, K
Nguyen, VH
Fucharoen, S
2015 PloS one
12 (10), pp. e0145230
114. Red blood cell microparticles in hemoglobin E disorders. Chaichote, W
Sae-Ung, N
Fucharoen, G
Fucharoen, S
2015 International journal of laboratory hematology
2 (37), pp. e52-5
115. Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening. Panyasai, S
Fucharoen, G
Fucharoen, S
2015 Clinica chimica acta; international journal of clinical chemistry
(438), pp. 226-30
116. Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women. Wongprachum, K
Sanchaisuriya, K
Dethvongphanh, M
Norcharoen, B
Htalongsengchan, B
Vidamaly, V
Sanchaisuriya, P
Fucharoen, S
Fucharoen, G
Schelp, FP
2015 Acta haematologica
2 (135), pp. 65-69
117. High resolution melting analytical platform for rapid prenatal and postnatal diagnosis of β-thalassemia common among Southeast Asian population. Prajantasen, T
Fucharoen, S
Fucharoen, G
2015 Clinica chimica acta; international journal of clinical chemistry
(441), pp. 56-62
118. Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome. Tepakhan, W
Yamsri, S
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2015 Annals of hematology
7 (94), pp. 1093-8
119. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization. Singha, K
Fucharoen, G
Hama, A
Fucharoen, S
2015 Clinical biochemistry
10 (48), pp. 703-8
120. Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia in Northeast Thailand. Yamsri, S
Pakdee, N
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2016 Acta haematologica
4 (136), pp. 233-239
121. FLT3-ITD Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand. Kumsaen, P
Fucharoen, G
Sirijerachai, C
Chainansamit, SO
Wisanuyothin, N
Kuwatjanakul, P
Wiangnon, S
2016 Asian Pacific journal of cancer prevention : APJCP
9 (17), pp. 4395-4399
122. Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder. Tepakhan, W
Yamsri, S
Sanchaisuriya, K
Fucharoen, G
Xu, X
Fucharoen, S
2016 Blood cells, molecules & diseases
(59), pp. 85-91
123. Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand. Prayalaw, P
Teawtrakul, N
Jetsrisuparb, A
Pongudom, S
Fucharoen, G
Fucharoen, S
2016 Acta haematologica
1 (135), pp. 15-20
124. Thalassemia Screening Using Different Automated Blood Cell Counters: Consideration of Appropriate Cutoff Values. Chaitraiphop, C
Sanchaisuriya, K
Inthavong, S
Fucharoen, G
Sanchaisuriya, P
Changtrakun, Y
Fucharoen, S
2016 Clinical laboratory
4 (62), pp. 545-52
125. Hemoglobin Variants in Northern Thailand: Prevalence, Heterogeneity and Molecular Characteristics. Panyasai, S
Fucharoen, G
Fucharoen, S
2016 Genetic testing and molecular biomarkers
1 (20), pp. 37-43
126. Screening of (-SEA) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies. Jomoui, W
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2017 Journal of clinical pathology
1 (70), pp. 63-68
127. Molecular analysis of haemoglobin E in Southeast Asian populations. Jomoui, W
Fucharoen, G
Sanchaisuriya, K
Nguyen, NT
Nguyen, HV
Fucharoen, S
2017 Annals of human biology
(), pp. 1-4
128. Novel interactions of two α-Hb variants with SEA deletion α(0)-thalassemia: hematological and molecular analyses. Srivorakun, H
Singha, K
Fucharoen, G
Fucharoen, S
2017 Hematology (Amsterdam, Netherlands)
(), pp. 1-5
129. Co-inheritance of α(0) -thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications. Singha, K
Srivorakun, H
Fucharoen, G
Fucharoen, S
2017 International journal of laboratory hematology
5 (39), pp. 508-512
130. Genetic origin of α(0)-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome. Jomoui, W
Fucharoen, G
Sanchaisuriya, K
Charoenwijitkul, P
Maneesarn, J
Xu, X
Fucharoen, S
2017 Journal of human genetics
8 (62), pp. 747-754
131. Evaluation of staff performance and interpretation of the screening program for prevention of thalassemia. Prommetta, S
Sanchaisuriya, K
Fucharoen, G
Yamsri, S
Chaiboonroeng, A
Fucharoen, S
2017 Biochemia medica
2 (27), pp. 387-397
132. Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups. Nguyen, NT
Sanchaisuriya, K
Sanchaisuriya, P
Van Nguyen, H
Phan, HTT
Fucharoen, G
Fucharoen, S
2017 Journal of community genetics
3 (8), pp. 221-228
133. Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system. Srivorakun, H
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2017 International journal of laboratory hematology
1 (39), pp. 101-111
134. Effect of health education on severe thalassemia prevention and control in communities in Cambodia. Cheng, K
Fucharoen, S
Sanchaisuriya, K
Fucharoen, G
Sanchaisuriya, P
Jetsrisuparb, A
2018 Archives of public health = Archives belges de sante publique
(76), pp. 13
135. EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin E-β0-thalassemia. Singha, K
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2018 Clinical chemistry and laboratory medicine
9 (56), pp. 1507-1513
136. Whole Blood PCR for Rapid Screening of α-Thalassemia. Wichian, P
Yamsri, S
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2018 Annals of clinical and laboratory science
2 (48), pp. 231-235
137. Clinical Course of Homozygous Hemoglobin Constant Spring in Pediatric Patients. Komvilaisak, P
Jetsrisuparb, A
Fucharoen, G
Komwilaisak, R
Jirapradittha, J
Kiatchoosakun, P
2018 Journal of pediatric hematology/oncology
5 (40), pp. 409-412
138. Prevalence of Thalassemia among Newborns: A Re-visited after 20 Years of a Prevention and Control Program in Northeast Thailand. Chaibunruang, A
Sornkayasit, K
Chewasateanchai, M
Sanugul, P
Fucharoen, G
Fucharoen, S
2018 Mediterranean journal of hematology and infectious diseases
1 (10), pp. e2018054
139. Elevations of Thrombotic Biomarkers in Hemoglobin H Disease. Chansai, S
Fucharoen, S
Fucharoen, G
Jetsrisuparb, A
Chumpia, W
2018 Acta haematologica
1 (139), pp. 47-51
140. Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand. Chaibunruang, A
Singha, K
Srivorakun, H
Fucharoen, G
Fucharoen, S
2018 Hemoglobin
(), pp. 1-5
141. Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam. Anh, TM
Sanchaisuriya, K
Kieu, GN
Tien, DN
Thu, HBT
Sanchaisuriya, P
Fucharoen, S
Fucharoen, G
Schelp, FP
2019 Hemoglobin
(), pp. 1-5
142. Molecular characteristics of α-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics. Charoenwijitkul, T
Singha, K
Fucharoen, G
Sanchaisuriya, K
Thepphitak, P
Wintachai, P
Karnpean, R
Fucharoen, S
2019 Clinical biochemistry
(71), pp. 31-37
143. Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G>A;92+7A>G]): a novel form of Hb E-β-thalassaemia syndrome. Singha, K
Fucharoen, G
Fucharoen, S
2019 Journal of clinical pathology
4 (72), pp. 322-324
144. Differentiation of homozygous hemoglobin E and hemoglobin E-β -thalassemia in children. Arong, A
Wangwok, G
Singha, K
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2019 International journal of laboratory hematology
3 (41), pp. e70-e72
145. Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia Disease without α-Thalassemia. Phanrahan, P
Yamsri, S
Teawtrakul, N
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2019 Mediterranean journal of hematology and infectious diseases
1 (11), pp. e2019038
146. Erythrocyte indices in a large cohort of β-thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia. Singha, K
Taweenan, W
Fucharoen, G
Fucharoen, S
2019 International journal of laboratory hematology
4 (41), pp. 513-518
147. Presentation of Compound Heterozygous Hemoglobin Constant Spring and Hemoglobin Pakse in Neonates. Komvilaisak, P
Jetsrisuparb, A
Fucharoen, G
Komwilaisak, R
Jirapradittha, J
Kiatchoosakun, P
2019 Journal of pediatric hematology/oncology
6 (41), pp. e413-e415
148. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α-Thalassemia. Pyae, AC
Srivorakun, H
Chaibunruang, A
Singha, K
Tomanakarn, K
Fucharoen, G
Fucharoen, S
2019 Hemoglobin
(), pp. 1-4
149. A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders. Jomoui, W
Tepakhan, W
Yamsri, S
Srivorakun, H
Fucharoen, G
Fucharoen, S
2020 Annals of hematology
1 (99), pp. 23-29
150. Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic. Singha, K
Srivorakun, H
Fucharoen, G
Fucharoen, S
2020 International journal of laboratory hematology
1 (42), pp. 23-27
151. Factors associated with anaemia and iron deficiency among women of reproductive age in Northeast Thailand: a cross-sectional study. Jamnok, J
Sanchaisuriya, K
Sanchaisuriya, P
Fucharoen, G
Fucharoen, S
Ahmed, F
2020 BMC public health
1 (20), pp. 102
152. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand. Nuntakarn, L
Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Jetsrisuparb, A
Wiangnon, S
Blood cells, molecules & diseases
1 (42), pp. 32-5
153. Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis. Pakdee, N
Yamsri, S
Fucharoen, G
Sanchaisuriya, K
Pissard, S
Fucharoen, S
Blood cells, molecules & diseases
1 (53), pp. 11-5
154. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis. Fucharoen, S
Fucharoen, G
Sae-ung, N
Sanchaisuriya, K
Blood cells, molecules & diseases
2 (39), pp. 195-8
155. Thalassemia and hemoglobinopathies rather than iron deficiency are major causes of pregnancy-related anemia in northeast Thailand. Sanchaisuriya, K
Fucharoen, S
Ratanasiri, T
Sanchaisuriya, P
Fucharoen, G
Dietz, E
Schelp, FP
Blood cells, molecules & diseases
1 (37), pp. 8-11
156. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: a molecular and hematological analysis. Fucharoen, S
Fucharoen, G
Sanchaisuriya, K
Surapot, S
Blood cells, molecules & diseases
2 (35), pp. 196-200
157. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies. Sedgewick, AE
Timofeev, N
Sebastiani, P
So, JC
Ma, ES
Chan, LC
Fucharoen, G
Fucharoen, S
Barbosa, CG
Vardarajan, BN
Farrer, LA
Baldwin, CT
Steinberg, MH
Chui, DH
Blood cells, molecules & diseases
3 (41), pp. 255-8

Title Authors Year Journal title Cited count
< 2015 2016 2017 2018 2019 2020 Total
1. Atypical hemoglobin H disease in a Thai patient resulting from a combination of alpha-thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity S Fucharoen
K Ayukarn
K Sanchaisuriya
G Fucharoen
2001 EUROPEAN JOURNAL OF HAEMATOLOGY
5.0 (66.0), pp. 312.0-316.0
21 0 0 0 0 0 21
2. Mitochondrial DNA polymorphisms in Thailand G Fucharoen
S Fucharoen
S Horai
2001 JOURNAL OF HUMAN GENETICS
3.0 (46.0), pp. 115.0-125.0
127 0 0 0 0 0 127
3. Molecular characterization of (delta beta)degrees/beta degrees-thalassemia and (delta beta)degrees-thalassemia/hemoglobin E in Thai patients S Fucharoen
Y Pengjam
S Surapot
G Fucharoen
K Sanchaisuriya
2001 EUROPEAN JOURNAL OF HAEMATOLOGY
4.0 (67.0), pp. 258.0-262.0
26 0 0 0 0 0 26
4. Molecular characterization of hemoglobin C in Thailand K Sanchaisuriya
G Fucharoen
N Sae-ung
N Siriratmanawong
S Surapot
S Fucharoen
2001 AMERICAN JOURNAL OF HEMATOLOGY
3.0 (67.0), pp. 189.0-193.0
38 0 0 0 0 0 38
5. Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients S Fucharoen
K Sanchaisuriya
G Fucharoen
S Surapot
2001 HAEMATOLOGICA
6.0 (86.0), pp. 657.0-658.0
16 0 0 0 0 0 16
6. Simultaneous PCR detection of beta-thalassemia and alpha-thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome N Siriratmanawong
G Fucharoen
K Sanchaisuriya
T Ratanasiri
S Fucharoen
2001 CLINICAL BIOCHEMISTRY
5.0 (34.0), pp. 377.0-380.0
78 0 0 0 0 0 78
7. A simplified screening for alpha-thalassemia 1 (SEA type) using a combination of a modified osmotic fragility test and a direct PCR on whole blood cell lysates S Panyasai
P Sringam
G Fucharoen
K Sanchaisuriya
S Fucharoen
2002 ACTA HAEMATOLOGICA
2.0 (108.0), pp. 74.0-78.0
54 0 0 0 0 0 54
8. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients Y Changtrakun
S Fucharoen
K Ayukarn
N Siriratmanawong
G Fucharoen
K Sanchaisuriya
2002 ANNALS OF HEMATOLOGY
7.0 (81.0), pp. 389.0-393.0
22 0 0 0 0 0 22
9. Frequency distribution and haplotypic heterogeneity of beta(E)-globin gene among eight minority groups of northeast Thailand G Fucharoen
S Fucharoen
K Sanchaisuriya
N Sae-ung
U Suyasunanond
P Sriwilai
P Chinorak
2002 HUMAN HEREDITY
1.0 (53.0), pp. 18.0-22.0
79 0 0 0 0 0 79
10. Hb Pakse [(alpha 2) codon 142(TAA -> TAT or Term -> Tyr)] in Thai patients with EABart's disease and Hb H disease K Sanchaisuriya
G Fucharoen
S Fucharoen
2002 HEMOGLOBIN
3.0 (26.0), pp. 227.0-235.0
93 0 0 0 0 0 93
11. Molecular analysis of a Thai beta-thalassaemia heterozygote with normal haemoglobin A(2) level: implication for population screening S Fucharoen
G Fucharoen
K Sanchaisuriya
Y Pengjam
2002 ANNALS OF CLINICAL BIOCHEMISTRY
(39.0), pp. 44.0-49.0
65 0 0 0 0 0 65
12. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion (G)gamma((A)gamma delta beta)(0)-thalassemia and (G)gamma((A)gamma delta beta)(0)-thalassemia/HbE in Thai patients S Fucharoen
Y Pengjam
S Surapot
G Fucharoen
K Sanchaisuriya
2002 AMERICAN JOURNAL OF HEMATOLOGY
2.0 (71.0), pp. 109.0-113.0
17 0 0 0 0 0 17
13. Molecular characterization of Hb D-Punjab [beta 121(GH4)Glu -> Gln] in Thailand S Fucharoen
Y Changtrakun
S Surapot
G Fucharoen
K Sanchaisuriya
2002 HEMOGLOBIN
3.0 (26.0), pp. 261.0-269.0
53 0 0 0 0 0 53
14. Molecular characterization of thalassemia intermedia associated with HPFH-6/beta-thalassemia and HPFH-6/Hb E in Thai patients S Fucharoen
G Fucharoen
K Sanchaisuriya
S Surapot
2002 ACTA HAEMATOLOGICA
3.0 (108.0), pp. 157.0-161.0
17 0 0 0 0 0 17
15. Paternal relationships of modern Asian populations, as viewed from the human Y-chromosomal DNA variation A Tajima
IH Pan
G Fucharoen
S Fucharoen
M Matsuo
K Tokunaga
T Juji
M Hayami
K Omoto
S Horai
2002 ANTHROPOLOGICAL SCIENCE
1.0 (110.0), pp. 120.0-120.0
0 0 0 0 0 0 0
16. Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia A Tajima
IH Pan
G Fucharoen
S Fucharoen
M Matsuo
K Tokunaga
T Juji
M Hayami
K Omoto
S Horai
2002 HUMAN GENETICS
1.0 (110.0), pp. 80.0-88.0
79 0 0 0 0 0 79
17. Triple heterozygosity of a hemoglobin variant: Hemoglobin Pyrgos with other hemoglobinopathies A Jetsrisuparb
K Sanchaisuriya
G Fucharoen
S Fucharoen
S Wiangnon
P Komwilaisak
2002 INTERNATIONAL JOURNAL OF HEMATOLOGY
1.0 (75.0), pp. 35.0-39.0
18 0 0 0 0 0 18
18. Complex interaction of Hb Hekinan [alpha 27(B8) Glu-Asp] and Hb E [beta 26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family S Fucharoen
Y Changtrakun
T Ratanasiri
G Fucharoen
K Sanchaisuriya
2003 EUROPEAN JOURNAL OF HAEMATOLOGY
5.0 (70.0), pp. 304.0-309.0
30 0 0 0 0 0 30
19. Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families S Fucharoen
K Sanchaisuriya
G Fucharoen
S Panyasai
R Devenish
L Luy
2003 HAEMATOLOGICA
10.0 (88.0), pp. 1092.0-1098.0
128 0 0 0 0 0 128
20. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand K Sanchaisuriya
G Fucharoen
N Sae-ung
A Jetsrisuparb
S Fucharoen
2003 ANNALS OF HEMATOLOGY
10.0 (82.0), pp. 612.0-616.0
111 0 0 0 0 0 111
21. Non-Invasive fetal sex determination using a conventional nested PCR analysis of fetal DNA in maternal plasma W Tungwiwat
G Fucharoen
T Ratanasiri
K Sanchaisuriya
S Fucharoen
2003 CLINICA CHIMICA ACTA
1-2 (334.0), pp. 173.0-177.0
39 0 0 0 0 0 39
22. Prenatal detection of fetal hemoglobin E gene from maternal plasma G Fucharoen
W Tungwiwat
T Ratanasiri
K Sanchaisuriya
S Fucharoen
2003 PRENATAL DIAGNOSIS
5.0 (23.0), pp. 393.0-396.0
57 0 0 0 0 0 57
23. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia G Fucharoen
K Sanchaisuriya
N Sae-Ung
S Dangwibul
S Fucharoen
2004 BULLETIN OF THE WORLD HEALTH ORGANIZATION
5.0 (82.0), pp. 364.0-372.0
196 0 0 0 0 0 196
24. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha 27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand S Chunpanich
K Ayukarn
K Sanchaisuriya
G Fucharoen
S Fucharoen
2004 CLINICAL AND LABORATORY HAEMATOLOGY
5.0 (26.0), pp. 355.0-358.0
3 0 0 0 0 0 3
25. Molecular basis and hematologic characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand S Panyasai
S Fucharoen
S Surapot
G Fucharoen
K Sanchaisuriya
2004 HAEMATOLOGICA
7.0 (89.0), pp. 777.0-781.0
29 0 0 0 0 0 29
26. Multiplex allele-specific PCR assay for differential diagnosis of Hb S, Hb D-punjab and Hb Tak K Sanchaisuriya
S Chunpanich
G Fucharoen
S Fucharoen
2004 CLINICA CHIMICA ACTA
1-2 (343.0), pp. 129.0-134.0
44 0 0 0 0 0 44
27. The diverse molecular basis and hematological features of Hb H and AEBart's diseases in northeast Thailand S Boonsa
K Sanchaisuriya
G Fucharoen
S Wiangnon
A Jetsrisuparb
S Fucharoen
2004 ACTA HAEMATOLOGICA
3.0 (111.0), pp. 149.0-154.0
119 0 0 0 0 0 119
28. A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy - An alternative approach to electronic blood cell counting K Sanchaisuriya
S Fucharoen
G Fucharoen
T Ratanasiri
P Sanchaisuriya
Y Changtrakul
U Ukosanakarn
U Ussawaphark
FP Schelp
2005 AMERICAN JOURNAL OF CLINICAL PATHOLOGY
1.0 (123.0), pp. 113.0-118.0
115 0 0 0 0 0 115
29. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb constant spring in pregnancy K Sanchaisuriya
S Chunpanich
S Fucharoen
G Fucharoen
P Sanchaisuriya
Y Changtrakun
2005 EUROPEAN JOURNAL OF HAEMATOLOGY
3.0 (74.0), pp. 221.0-227.0
42 0 0 0 0 0 42
30. Compound heterozygote state for (G)gamma(A)gamma(delta beta)degrees-thalassemia and hereditary persistence of fetal hemoglobin S Fucharoen
S Panyasai
S Surapot
G Fucharoen
K Sanchaisuriya
2005 AMERICAN JOURNAL OF HEMATOLOGY
2.0 (80.0), pp. 119.0-123.0
2 0 0 0 0 0 2
31. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: A molecular and hematological analysis S Fucharoen
G Fucharoen
K Sanchaisuriya
S Surapot
2005 BLOOD CELLS MOLECULES AND DISEASES
2.0 (35.0), pp. 196.0-200.0
8 0 0 0 0 0 8
32. Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients S Fucharoen
S Singsanan
K Sanchaisuriya
G Fucharoen
2005 CLINICAL AND LABORATORY HAEMATOLOGY
3.0 (27.0), pp. 184.0-189.0
18 0 0 0 0 0 18
33. Thalassemia intermedia associated with complex interaction of Hb Beijing [alpha 16(A14)Lys -> Asn] and Hb E [beta 26(B8)Glu -> Lys] with a deletional alpha-thalassemia-1 in a Thai family S Fucharoen
S Chunpanich
K Sanchaisuriya
G Fucharoen
N Kunyanone
2005 HEMOGLOBIN
1.0 (29.0), pp. 77.0-83.0
14 0 0 0 0 0 14
34. Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma Warunee Tungwiwat
Supan Fucharcoen
Goonnapa Fucharoen
Thawalwong Ratanasiri
Kanokwan Sanchaisuriya
2006 CIRCULATING NUCLEIC ACIDS IN PLASMA AND SERUM IV
(1075.0), pp. 103.0-107.0
49 0 0 0 0 0 49
35. Development of severe anemia during fever episodes in patients with hemoglobin E trait and hemoglobin H disease combinations A Jetsrisuparb
K Sanchaisuriya
G Fucharoen
S Fucharoen
S Wiangnon
C Jetsrisuparb
J Sirijirachai
K Chansoong
2006 JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
4.0 (28.0), pp. 249.0-253.0
20 0 0 0 0 0 20
36. Molecular and hematological profiles of hemoglobin EE disease with different forms of alpha-thalassemia G Fucharoen
J Trithipsombat
S Sirithawee
S Yamsri
Y Changtrakul
K Sanchaisuriya
S Fucharoen
2006 ANNALS OF HEMATOLOGY
7.0 (85.0), pp. 450.0-454.0
76 0 0 0 0 0 76
37. Thalassemia and hemoglobinopathies rather than iron deficiency are major causes of pregnancy-related anemia in northeast Thailand Kanokwan Sanchaisuriya
Supan Fucharoen
Thawalwong Ratanasiri
Pattara Sanchaisuriya
Goonnapa Fucharoen
Ekkahart Dietz
Frank P. Schelp
2006 BLOOD CELLS MOLECULES AND DISEASES
1.0 (37.0), pp. 8.0-11.0
50 0 0 0 0 0 50
38. alpha(0)-thalassemia and related disorders in northeast Thailand: A molecular and hematological characterization Nattaya Sae-ung
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2007 ACTA HAEMATOLOGICA
2.0 (117.0), pp. 78.0-82.0
73 0 0 0 0 0 73
39. alpha/beta-globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function Chulaporn Chaisue
Suttiphan Kitcharoen
Prapon Wilairat
Arunee Jetsrisuparb
Goonnapa Fucharoen
Supan Fucharoen
2007 CLINICAL BIOCHEMISTRY
18.0 (40.0), pp. 1373.0-1377.0
34 0 0 0 0 0 34
40. Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia Warunee Tungwiwat
Goonnapa Fucharoen
Supan Fucharoen
Thawalwong Ratanasiri
Kanokwan Sanchaisuriya
Natraya Sae-Ung
2007 TRANSLATIONAL RESEARCH
5.0 (150.0), pp. 319.0-325.0
28 0 0 0 0 0 28
41. Coexistence of Southeast Asian ovalocytosis and beta-thalassemia: A molecular and hematological analysis Goonnapa Fucharoen
Supan Fucharoen
Sanita Singsanan
Kanokwan Sanchaisuriya
2007 AMERICAN JOURNAL OF HEMATOLOGY
5.0 (82.0), pp. 381.0-385.0
11 0 0 0 0 0 11
42. Cutoff values of Hb E and MCV for screening of double heterozygosity for Hb E/alpha(0)-thalassemia Kanokwan Sanchaisuriya
Sunisa Chirakul
Hataichanok Srivorakun
Goonnapa Fucharoen
Yossombat Changtrakun
Supan Fucharoen
2007 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
(29.0), pp. 109.0-110.0
0 0 0 0 0 0 0
43. Effect of the maternal beta(E)-globin gene on hematologic responses to iron supplementation during pregnancy Kanokwan Sanchaisuriya
Supan Fucharoen
Thawalwong Ratanasiri
Pattara Sanchaisuriya
Goonnapa Fucharoen
Ekkehart Dietz
Frank P. Schelp
2007 AMERICAN JOURNAL OF CLINICAL NUTRITION
2.0 (85.0), pp. 474.0-479.0
6 0 0 0 0 0 6
44. Evaluation of the fetal sex prediction using a conventional PCR analysis of DNA in maternal plasma Warunee Tungwiwat
Goonnapa Fucharoen
Supan Fucharoen
Thawalwong Ratanasiri
Kanokwan Sanchaisuriya
Nattaya Sae-Ung
2007 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
(29.0), pp. 110.0-110.0
0 0 0 0 0 0 0
45. H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers Supawadee Yamsri
Kanokwan Sanchaisuriya
Supan Fucharoen
Goonnapa Fucharoen
Arunee Jetsrisuparb
Surapon Wiangnon
Yossombat Changtrakul
Pattara Sanchaisuriya
2007 ACTA HAEMATOLOGICA
2.0 (118.0), pp. 99.0-105.0
17 0 0 0 0 0 17
46. High prevalence of alpha thalassemia in Thai families with beta thalassemia: Molecular and hematological analysis Goonnapa Fucharoen
Yossombat Changtrakul
Kanokwan Sanchaisuriya
Nattaya Sae-Ung
Supan Fucharoen
Arunee Jetsrisuparb
2007 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
(29.0), pp. 105.0-105.0
0 0 0 0 0 0 0
47. Molecular and hematological features of the Hb constant spring EE bart's disease Supan Fucharoen
Goonnapa Fucharoen
Nattaya Sae-Ung
Kanokwan Sanchaisuriya
2007 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
(29.0), pp. 104.0-105.0
0 0 0 0 0 0 0
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Goonnapa Fucharoen
Onekham Savongsy
Kanokwan Sanchaisuriya
Supan Fucharoen
2007 ANNALS OF HEMATOLOGY
9.0 (86.0), pp. 665.0-669.0
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49. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha degrees-thalassemia determinants Nirut Siriratmanawong
Charnchai Pinmuang-Ngam
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Supan Fucharoen
2007 FETAL DIAGNOSIS AND THERAPY
4.0 (22.0), pp. 264.0-268.0
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Abdulloh Hama
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Kanokwan Sanchaisuriya
2007 CLINICAL BIOCHEMISTRY
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Nattaya Sae-ung
Kanokwan Sanchaisuriya
2007 BLOOD CELLS MOLECULES AND DISEASES
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Kanokwan Sanchaisuriya
2008 AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY
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R. Karnpean
S. Fucharoen
N. Sae-Ung
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2008 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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Nadia Timofeev
Paola Sebastiani
Jason C. C. So
Edmond S. K. Ma
Li Chong Chan
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Supan Fucharoen
Cynara G. Barbosa
Badri N. Vardarajan
Lindsay A. Farrer
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Martin H. Steinberg
David H. K. Chui
2008 BLOOD CELLS MOLECULES AND DISEASES
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55. Effective screening for double heterozygosity of Hb E/alpha(0)-thalassemia Kanokwan Sanchaisuriya
Sunisa Chirakul
Hataichanok Srivorakun
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Supan Fucharoen
Yossombat Changtrakul
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2008 ANNALS OF HEMATOLOGY
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56. Effective screening for thalassemia and hemoglobinopathies among pregnant Laos women S. Fucharoen
O. Savongsy
G. Fucharoen
K. Sanchaisuriya
N. Sae-ung
2008 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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57. Effect of alpha (0)-thalassemia, beta-thalassemia and hemoglobin E genes on anemia: comparison between males and females S. Yamsri
K. Sanchaisuriya
G. Fucharoen
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N. Sae-ung
A. Jetsrisuparp
2008 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
(30.0), pp. 136.0-136.0
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S. Yamsri
S. Fucharoen
G. Fucharoen
P. Sanchaisuriya
O. Savongse
R. Devenish
2008 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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Kanokwan Sanchaisuriya
Supan Fucharoen
Goonnapa Fucharoen
Nirut Siriratmanawong
Charnchai Pinmuang-ngam
Pattara Sanchaisuriya
2008 ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
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60. Interactions of Hb Q-Thailand with various hemoglobinopathies: molecular and hemoglobin analysis S. Singsanan
G. Fucharoen
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S. Yamsri
K. Sanchaisuriya
N. Sae-ung
2008 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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61. Stability of red blood cell parameters in carriers of alpha-thalassemia, beta-thalassemia and hemoglobin E N. Sae-ung
K. Soontornwisai
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K. Sanchaisuriya
S. Fucharoen
2008 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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Supan Fucharoen
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Nattaya Sae-ung
2008 ANNALS OF HEMATOLOGY
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63. Accurate Prenatal Diagnosis of Hb Bart's Hydrops Fetalis in Daily Practice with a Double-Check PCR System Rossarin Karnpean
Goonnapa Fucharoen
Supan Fucharoen
Nattaya Sae-ung
Kanokwan Sanchaisuriya
Thawalwong Ratanasiri
2009 ACTA HAEMATOLOGICA
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64. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases Hataichanok Srivorakun
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Nattaya Sae-Ung
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Thawalwong Ratanasiri
Supan Fucharoen
2009 EUROPEAN JOURNAL OF HAEMATOLOGY
1.0 (83.0), pp. 57.0-65.0
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65. COMPLEX INTERACTION OF Hb E [beta 26(B8)Glu -> Lys], Hb KORLE-BU [beta 73(E17)Asp -> Asn] AND A DELETIONAL alpha-THALASSEMIA-1 IN PREGNANCY Nirut Siriratmanawong
Wichuda Chansri
Sanita Singsanan
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Supan Fucharoen
2009 HEMOGLOBIN
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66. EFFECT OF IRON FORTIFIED MILK ON HEMATOLOGICAL CHANGES IN NON-IRON DEFICIENT THAI-SCHOOL CHILDREN K. Sanchaisuriya
N. Panomai
P. Sanchaisuriya
S. Lowirakorn
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S. Fucharoen
F. Schelp
2009 HAEMATOLOGICA-THE HEMATOLOGY JOURNAL
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67. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand Lalana Nuntakarn
Supan Fucharoen
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Arunee Jetsrisuparb
Surapon Wiangnon
2009 BLOOD CELLS MOLECULES AND DISEASES
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68. Prenatal Diagnosis of Hemoglobin Bart's Hydrops Fetalis with Gap-PCR System Response Rossarin Karnpean
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Kanokwan Sanchaisuriya
Thawalwong Ratanasiri
2009 ACTA HAEMATOLOGICA
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69. Compound Heterozygous Hb Tak/Hb E Causes Secondary Erythrocytosis in a Thai Family Nattiya Teawtrakul
Chittima Sirijirachai
Ganjana Chansung
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2010 HEMOGLOBIN
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2010 BLOOD CELLS MOLECULES AND DISEASES
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71. Improvement of alpha(0) - Thalassemia Screening Using Combined Osmotic Fragility, Dichlorophenolindophenol and Hb H Inclusion Tests Attawut Chaibunruang
Sontong Pornphannukool
Nattaya Sae-Ung
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Supan Fucharoen
2010 CLINICAL LABORATORY
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72. Interactions of hemoglobin Lepore (delta beta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis Attawut Chaibunruang
Hataichanok Srivorakun
Suplan Fucharoen
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Nattaya Sae-ung
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2010 BLOOD CELLS MOLECULES AND DISEASES
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73. Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center Supawadee Yamsri
Kanokwan Sanchaisuriya
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2010 PRENATAL DIAGNOSIS
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74. Secondary Erythrocytosis Caused by Hemoglobin Tak/(delta beta)(0)-Thalassemia Syndrome Nattaphol Prakobkaew
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Satja Surapot
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2010 ACTA HAEMATOLOGICA
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75. Thalassemia and iron deficiency in a group of northeast Thai school children: relationship to the occurrence of anemia Nichathorn Panomai
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2010 EUROPEAN JOURNAL OF PEDIATRICS
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76. Anemia, Iron Deficiency and Thalassemia among Adolescents in Northeast Thailand: Results from Two Independent Surveys Anupong Pansuwan
Goonnapa Fucharoen
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Boonmee Himakhun
Samrit Dangwiboon
2011 ACTA HAEMATOLOGICA
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77. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [alpha 63(E12)Ala -> Val], a novel alpha 2-globin chain variant with Hb E [beta 26(B8)Glu -> Lys] and a deletional alpha(+)-thalassemia Hataichanok Srivorakun
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Napat Kheawon
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2011 EUROPEAN JOURNAL OF HAEMATOLOGY
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2011 CLINICAL BIOCHEMISTRY
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2011 BLOOD CELLS MOLECULES AND DISEASES
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2011 HEMOGLOBIN
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2011 ANNALS OF HEMATOLOGY
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2011 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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Patcharee Komwilaisak
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2011 CLINICAL BIOCHEMISTRY
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Attawut Chaibunruang
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2012 ANNALS OF CLINICAL BIOCHEMISTRY
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2012 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2012 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2012 HEMOGLOBIN
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2012 TRANSLATIONAL RESEARCH
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2012 HEMOGLOBIN
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2012 HEMOGLOBIN
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2012 BLOOD CELLS MOLECULES AND DISEASES
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2012 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2012 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2012 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2012 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2013 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2013 CLINICAL CHEMISTRY AND LABORATORY MEDICINE
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2013 HEMOGLOBIN
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2013 ACTA HAEMATOLOGICA
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2013 FETAL DIAGNOSIS AND THERAPY
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2013 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2013 CLINICAL BIOCHEMISTRY
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2013 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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2016 ACTA HAEMATOLOGICA
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2020 BMC PUBLIC HEALTH
1.0 (20.0), pp.
0 0 0 0 0 0 0
179. Hemoglobins F, A(2), and E levels in Laotian children aged 6-23 months with Hb E disorders: Effect of age, sex, and thalassemia types Benchawan Kingchaiyaphum
Kanokwan Sanchaisuriya
Goonnapa Fucharoen
Attawut Chaibunruang
Sonja Y. Hess
Guy-Marino Hinnouho
Maxwell A. Barffour
Kimbery R. Wessells
Sengchanh Kounnavong
Supan Fucharoen
2020 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
(), pp.
0 0 0 0 0 0 0
180. Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic Kritsada Singha
Hataichanok Srivorakun
Goonnapa Fucharoen
Supan Fucharoen
2020 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
1.0 (42.0), pp. 23.0-27.0
1 0 0 0 0 0 1

Title Authors Year Journal title
1. Identification of Hb S in Thai patients Y Changtrakun
V Suksa-ard
G Fucharoen
K Sanchaisuriya
S Fucharoen
2002 Journal of Health Science and Medical Research
(20 No 3), pp. 201-209

Title Authors NRIIS type Year NRIIS Scholarship

0.06803226470947266