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ผศ. หทัยชนก  ศรีวรกุล

ผศ. หทัยชนก ศรีวรกุล

คณะเทคนิคการแพทย์,
มหาวิทยาลัยขอนแก่น
24391468400: H-INDEX 9

บทความ

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

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SCOPUS

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PUBMED

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ISI

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TCI

Title Author Year SCOPUS PUBMED ISI TCI
1. 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
2. Effective screening for double heterozygosity of Hb E/α0 -thalassemia Sanchaisuriya, K
Chirakul, S
Srivorakun, H
Fucharoen, G
Fucharoen, S
Changtrakul, Y
Sanchaisuriya, P
2008
3. 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
4. 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
5. 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
6. 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
7. 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
8. 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
9. 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
10. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system Fucharoen, G.
Srivorakun, H.
Singsanan, S.
Fucharoen, S.P.
2011
11. Thalassemia and hemoglobinopathies in Southeast Asian newborns: Diagnostic assessment using capillary electrophoresis system Hataichanok Srivorakun
Goonnapa Fucharoen
Yossombat Changtrakul
Patcharee Komwilaisak
Supan Fucharoen
2011
12. 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
13. 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
14. 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
15. 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
16. 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
17. A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration. Hataichanok Srivorakun
Kritsada Singha
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2014
18. 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
19. Co-inheritance of α0-thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications Singha, K.
Srivorakun, H.
Fucharoen, G.
2017
20. Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system Srivorakun, H.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2017
21. 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
22. 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
23. 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
24. 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
25. 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
26. 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
27. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of alpha(+)-Thalassemia Aye Chan Pyae
Hataichanok Srivorakun
Attawut Chaibunruang
Kritsada Singha
Kanchana Tomanakarn
Goonnapa Fucharoen
Supan Fucharoen
2019
28. 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
29. 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
30. 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
31. A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders Wittaya Jomoui
Wanicha Tepakhan
Supawadee Yamsri
Hataichanok Srivorakun
Goonnapa Fucharoen
Supan Fucharoen
2020
32. 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
33. β-Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program. Kritsada Singha
Attawut Chaibunruang
Bounpalisone Souvanlasy
Hataichanok Srivorakun
Supawadee Yamsri
Goonnapa Fucharoen
Supan Fucharoen
2021
34. Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis. Phongsathorn Wichian
Supawadee Yamsri
Attawut Chaibunruang
Cholthicha KerdKaew
Dhanawan Thongsee
Hataichanok Srivorakun
Supan Fucharoen
2021
35. α-thalassemia in affected fetuses with hemoglobin E-β-thalassemia disease in a high-risk population in Thailand. Yamsri, S
Prommetta, S
Srivorakun, H
Taweenan, W
Sanchaisuriya, K
Chaibunruang, A
Fucharoen, G
Fucharoen, S
2022
36. Diagnostic value of fetal hemoglobin Bart’s for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy Singha, K
Yamsri, S
Chaibunruang, A
Srivorakun, H
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2022
37. Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis. Jomoui, W
Srivorakun, H
Chansai, S
Fucharoen, S
2022
38. Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis Srivorakun, H.
Chansai, S.
Fucharoen, S.P.
2022
39. Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A2 in the Thai population Srivorakun, H.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2022
40. Thalassemia and erythroid transcription factor mutations associated with borderline hemoglobin A in the Thai population. Srivorakun, H
Thawinan, W
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2022
Count 23 21 20 0

Title Authors Year Publication name Cited count
< 2017 2018 2019 2020 2021 2022 รวม
1. 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
2. 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
3. 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
4. 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
5. 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
6. 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
7. 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
8. 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
9. 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
10. 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.
11. 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
12. 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
13. 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
14. 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
15. 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
16. 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
17. 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
18. 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
19. Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis Wichian, P.
Yamsri, S.
Chaibunruang, A.
Srivorakun, H.
Fucharoen, S.P.
2021 Scandinavian Journal of Clinical and Laboratory Investigation
7 (81), pp. 557-563
20. β-Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program Singha, K.
Chaibunruang, A.
Srivorakun, H.
Yamsri, S.
Fucharoen, G.
Fucharoen, S.P.
2021 International Journal of Laboratory Hematology
3 (43), pp. 500-505
21. Diagnostic value of fetal hemoglobin Bart’s for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy Singha, K.
Yamsri, S.
Chaibunruang, A.
Srivorakun, H.
Sanchaisuriya, K.
Fucharoen, G.
Fucharoen, S.P.
2022 Orphanet Journal of Rare Diseases
1 (17), pp.
22. Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α<sup>0</sup>-thalassemia: Application to population screening and prenatal diagnosis Srivorakun, H.
Chansai, S.
Fucharoen, S.P.
2022 PLoS ONE
4 April (17), pp.
23. Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A<inf>2</inf> in the Thai population Srivorakun, H.
Fucharoen, G.
Sanchaisuriya, K.
Fucharoen, S.P.
2022 Archives of Medical Science
1 (18), pp. 112-120

Title Authors Year Journal title
1. 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
2. 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
3. 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
4. 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
5. 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
6. 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
7. 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
8. 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
9. 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
10. 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
11. 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
12. 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
13. 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
14. 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
15. 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
16. β-Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program. Singha, K
Chaibunruang, A
Souvanlasy, B
Srivorakun, H
Yamsri, S
Fucharoen, G
Fucharoen, S
2021 International journal of laboratory hematology
3 (43), pp. 500-505
17. Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis. Wichian, P
Yamsri, S
Chaibunruang, A
KerdKaew, C
Thongsee, D
Srivorakun, H
Fucharoen, S
2021 Scandinavian journal of clinical and laboratory investigation
(), pp. 1-7
18. Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis. Jomoui, W
Srivorakun, H
Chansai, S
Fucharoen, S
2022 PloS one
4 (17), pp. e0267832
19. Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy. Singha, K
Yamsri, S
Chaibunruang, A
Srivorakun, H
Sanchaisuriya, K
Fucharoen, G
Fucharoen, S
2022 Orphanet journal of rare diseases
1 (17), pp. 45
20. Thalassemia and erythroid transcription factor mutations associated with borderline hemoglobin A in the Thai population. Srivorakun, H
Thawinan, W
Fucharoen, G
Sanchaisuriya, K
Fucharoen, S
2022 Archives of medical science : AMS
1 (18), pp. 112-120
21. α-thalassemia in affected fetuses with hemoglobin E-β-thalassemia disease in a high-risk population in Thailand. Yamsri, S
Prommetta, S
Srivorakun, H
Taweenan, W
Sanchaisuriya, K
Chaibunruang, A
Fucharoen, G
Fucharoen, S
2022 American journal of translational research
2 (14), pp. 1315-1323

Title Authors Year Journal title Cited count
< 2017 2018 2019 2020 2021 2022 รวม
1. 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
2. Effective screening for double heterozygosity of Hb E/alpha(0)-thalassemia Kanokwan Sanchaisuriya
Sunisa Chirakul
Hataichanok Srivorakun
Goonnapa Fucharoen
Supan Fucharoen
Yossombat Changtrakul
Pattara Sanchaisuriya
2008 ANNALS OF HEMATOLOGY
11.0 (87.0), pp. 911.0-914.0
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3. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases Hataichanok Srivorakun
Goonnapa Fucharoen
Nattaya Sae-Ung
Kanokwan Sanchaisuriya
Thawalwong Ratanasiri
Supan Fucharoen
2009 EUROPEAN JOURNAL OF HAEMATOLOGY
1.0 (83.0), pp. 57.0-65.0
50 0 0 0 0 0 50
4. 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
Goonnapa Fucharoen
Nattaya Sae-ung
Kanokwan Sanchaisuriya
2010 BLOOD CELLS MOLECULES AND DISEASES
3.0 (44.0), pp. 140.0-145.0
25 0 0 0 0 0 25
5. 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 EUROPEAN JOURNAL OF HAEMATOLOGY
1.0 (87.0), pp. 68.0-72.0
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6. 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 HEMOGLOBIN
2.0 (35.0), pp. 103.0-110.0
11 0 0 0 0 0 11
7. Thalassemia and hemoglobinopathies in Southeast Asian newborns: diagnostic assessment using capillary electrophoresis system Hataichanok Srivorakun
Goonnapa Fucharoen
Yossombat Changtrakul
Patcharee Komwilaisak
Supan Fucharoen
2011 CLINICAL BIOCHEMISTRY
5-6 (44.0), pp. 406.0-411.0
30 0 0 0 0 0 30
8. Phenotypic expression of hemoglobins A(2), E and F in various hemoglobin E related disorders Nattaya Sae-ung
Hataichanok Srivorakun
Goonnapa Fucharoen
Supawadee Yamsri
Kanokwan Sanchaisuriya
Supan Fucharoen
2012 BLOOD CELLS MOLECULES AND DISEASES
1.0 (48.0), pp. 11.0-16.0
41 0 0 0 0 0 41
9. 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 HEMOGLOBIN
1.0 (37.0), pp. 37.0-47.0
14 0 0 0 0 0 14
10. 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 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
(35.0), pp. 98.0-98.0
0 0 0 0 0 0 0
11. A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration Hataichanok Srivorakun
Kritsada Singha
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2014 PLOS ONE
9.0 (9.0), pp.
28 0 0 0 0 0 28
12. ARKRAY ADAMS A1c HA-8180T Analyzer for Diagnosis of Thalassemia and Hemoglobinopathies Common in Southeast Asia Jatuphol Kunwandee
Hataichanok Srivorakun
Goonnapa Fucharoen
Kanokwan Sanchaisuriya
Supan Fucharoen
2014 LABMEDICINE
3.0 (45.0), pp. E112-E121
4 0 0 0 0 0 4
13. 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 HEMOGLOBIN
1.0 (42.0), pp. 11.0-15.0
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14. 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 HEMATOLOGY
3.0 (23.0), pp. 187.0-191.0
3 0 0 0 0 0 3
15. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of alpha(+)-Thalassemia Aye Chan Pyae
Hataichanok Srivorakun
Attawut Chaibunruang
Kritsada Singha
Kanchana Tomanakarn
Goonnapa Fucharoen
Supan Fucharoen
2019 HEMOGLOBIN
4-5 (43.0), pp. 254.0-257.0
4 0 0 0 0 0 4
16. 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 HEMOGLOBIN
(), pp.
5 0 0 0 0 0 5
17. A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders Wittaya Jomoui
Wanicha Tepakhan
Supawadee Yamsri
Hataichanok Srivorakun
Goonnapa Fucharoen
Supan Fucharoen
2020 ANNALS OF HEMATOLOGY
1.0 (99.0), pp. 23.0-29.0
1 0 0 0 0 0 1
18. 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
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19. beta-Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program Kritsada Singha
Attawut Chaibunruang
Bounpalisone Souvanlasy
Hataichanok Srivorakun
Supawadee Yamsri
Goonnapa Fucharoen
Supan Fucharoen
2021 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
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20. Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis Phongsathorn Wichian
Supawadee Yamsri
Attawut Chaibunruang
Cholthicha KerdKaew
Dhanawan Thongsee
Hataichanok Srivorakun
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2021 SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
7.0 (81.0), pp. 557.0-563.0
0 0 0 0 0 0 0

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