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 Hataichanok Srivorakun

Hataichanok Srivorakun

Faculty of Associated Medical Sciences,
Khon Kaen University
24391468400: H-INDEX 9

Documents

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

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TCI

Title Author Year SCOPUS PUBMED ISI TCI
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
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
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
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
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
6. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system Fucharoen, G.
Srivorakun, H.
Singsanan, S.
Fucharoen, S.P.
2011
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
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
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
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
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
12. Co-inheritance of α0-thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications Singha, K.
Srivorakun, H.
Fucharoen, G.
2017
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
14. 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
15. 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
16. 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
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
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
19. 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
20. 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
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
22. 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
23. 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
Count 23 0 0 0

Title Authors Year Publication name Cited count
< 2017 2018 2019 2020 2021 2022 Total
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

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Title Authors Year Journal title Cited count
< 2017 2018 2019 2020 2021 2022 Total

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0.03177523612976074