| 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/alpha0-thalassemia. | Kanokwan Sanchaisuriya Sunisa Chirakul Hataichanok Srivorakun Goonnapa Fucharoen Supan Fucharoen Yossombat Changtrakul Pattara Sanchaisuriya |
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 (deltabeta 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 | ||||
| 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. Fucharoen, S.P. |
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. Fucharoen, S.P. |
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 | Srivorakun, H Fucharoen, G Changtrakul, Y Komwilaisak, P Fucharoen, S |
2011 | ||||
| 12. | Phenotypic expression of hemoglobins A2, E and F in various hemoglobin E related disorders | Nattaya Sae-ung Hataichanok Srivorakun Goonnapa Fucharoen Supawadee Yamsri Kanokwan Sanchaisuriya Supan Fucharoen |
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. | 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 | ||||
| 17. | 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 | ||||
| 18. | 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 | ||||
| 19. | 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 | ||||
| 20. | Co-inheritance of α0-thalassemia elevates Hb A |
Singha, K. Srivorakun, H. Fucharoen, G. |
2017 | ||||
| 21. | Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system | Srivorakun, H. Fucharoen, G. Sanchaisuriya, K. Fucharoen, S.P. |
2017 | ||||
| 22. | 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 | ||||
| 23. | 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 | ||||
| 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 |
2018 | ||||
| 25. | 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 | ||||
| 26. | 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 | ||||
| 27. | 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 | ||||
| 28. | 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 | ||||
| 29. | 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 | ||||
| 30. | 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 | ||||
| 31. | 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 | ||||
| 32. | 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 | ||||
| 33. | 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 | ||||
| 34. | beta-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 | ||||
| 35. | 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 | ||||
| 36. | 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 | ||||
| 37. | 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 | ||||
| 38. | 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 | ||||
| 39. | 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 | ||||
| 40. | Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A |
Srivorakun, H. Fucharoen, G. Sanchaisuriya, K. Fucharoen, S.P. |
2022 | ||||
| 41. | 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 | ||||
| 42. | A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation. | Singha, K Tepakhan, W Yamsri, S Chaibunruang, A Srivorakun, H Pansuwan, A Fucharoen, G Fucharoen, S |
2023 | ||||
| 43. | Anemia in an ethnic minority group in lower northern Thailand: A community-based study investigating the prevalence in relation to inherited hemoglobin disorders and iron deficiency. | Pyae, TW Sanchaisuriya, K Athikamanon, S Sanchaisuriya, P Srivorakun, H Chaibunruang, A Fucharoen, S |
2023 | ||||
| 44. | Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program. | Singha, K. Yamsri, S. Chaibunruang, A. Srivorakun, H. Sanchaisuriya, K. Fucharoen, G. Fucharoen, S. |
2023 | ||||
| 45. | Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression | Arong, A. Srivorakun, H. Chaibunruang, A. Fucharoen, S. Fucharoen, G. Kounnavong, S. Sanchaisuriya, K. |
2023 | ||||
| 46. | Molecular basis of a high Hb A/Hb F-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with -globin gene triplication. | Soontornpanawet, C Singha, K Srivorakun, H Tepakhan, W Fucharoen, G Fucharoen, S |
2023 | ||||
| 47. | Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A levels or hemoglobin A variants: A single center experience. | Hanart, C Singha, K Changtrakul, Y Fucharoen, S Srivorakun, H |
2023 | ||||
| 48. | A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation. | Singha, K Tepakhan, W Yamsri, S Chaibunruang, A Srivorakun, H Pansuwan, A Fucharoen, G Fucharoen, S |
2024 | ||||
| 49. | Fetal hematological phenotypes of various hemoglobinopathies and demonstration of embryonic hemoglobins on capillary electrophoresis: a large cohort data from prenatal screening program. | Singha, K Yamsri, S Chaibunruang, A Srivorakun, H Pansuwan, A Sanchaisuriya, K Fucharoen, G Fucharoen, S |
2025 | ||||
| 50. | Multiplex recombinase polymerase amplification (RPA) assay for carrier detection and prenatal diagnosis of α0-thalassemia (SEA and THAI deletions) | Sitthisophonkamjorn, Y. Prommetta, S. Chaibunruang, A. Srivorakun, H. Fucharoen, S. Yamsri, S. |
2025 | ||||
| 51. | Multiplex recombinase polymerase amplification (RPA) assay for carrier detection and prenatal diagnosis of α-thalassemia (SEA and THAI deletions). | Sitthisophonkamjorn, Y Prommetta, S Chaibunruang, A Srivorakun, H Fucharoen, S Yamsri, S |
2025 | Count | 26 | 29 | 20 | 0 |
| Title | Authors | Year | Publication name | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | 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<sup>;0</sup>-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>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 |
||||||||
| 24. | Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program | Singha, K. Yamsri, S. Chaibunruang, A. Srivorakun, H. Sanchaisuriya, K. Fucharoen, G. Fucharoen, S. |
2023 |
PLoS ONE 4 APRIL (18), pp. |
||||||||
| 25. | Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression | Arong, A. Srivorakun, H. Chaibunruang, A. Fucharoen, S. Fucharoen, G. Kounnavong, S. Sanchaisuriya, K. |
2023 |
International Journal of Laboratory Hematology 3 (45), pp. 387-393 |
||||||||
| 26. | Multiplex recombinase polymerase amplification (RPA) assay for carrier detection and prenatal diagnosis of α0-thalassemia (SEA and THAI deletions) | Sitthisophonkamjorn, Y. Prommetta, S. Chaibunruang, A. Srivorakun, H. Fucharoen, S. Yamsri, S. |
2025 |
Scandinavian Journal of Clinical and Laboratory Investigation 1 (85), pp. 78-84 |
||||||||
| 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. | 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 |
|
| 15. | 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 |
|
| 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. | 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 |
|
| 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. | 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 |
|
| 22. | Molecular basis of a high Hb A/Hb F-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with -globin gene triplication. | Soontornpanawet, C Singha, K Srivorakun, H Tepakhan, W Fucharoen, G Fucharoen, S |
2023 |
PeerJ (11), pp. e15308 |
|
| 23. | Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program. | Singha, K Yamsri, S Chaibunruang, A Srivorakun, H Sanchaisuriya, K Fucharoen, G Fucharoen, S |
2023 |
PloS one 4 (18), pp. e0283051 |
|
| 24. | A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation. | Singha, K Tepakhan, W Yamsri, S Chaibunruang, A Srivorakun, H Pansuwan, A Fucharoen, G Fucharoen, S |
2023 |
Clinica chimica acta; international journal of clinical chemistry (), pp. 117615 |
|
| 25. | Anemia in an ethnic minority group in lower northern Thailand: A community-based study investigating the prevalence in relation to inherited hemoglobin disorders and iron deficiency. | Pyae, TW Sanchaisuriya, K Athikamanon, S Sanchaisuriya, P Srivorakun, H Chaibunruang, A Fucharoen, S |
2023 |
PloS one 6 (18), pp. e0287527 |
|
| 26. | Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A levels or hemoglobin A variants: A single center experience. | Hanart, C Singha, K Changtrakul, Y Fucharoen, S Srivorakun, H |
2023 |
Clinica chimica acta; international journal of clinical chemistry (), pp. 117417 |
|
| 27. | A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation. | Singha, K Tepakhan, W Yamsri, S Chaibunruang, A Srivorakun, H Pansuwan, A Fucharoen, G Fucharoen, S |
2024 |
Clinica chimica acta; international journal of clinical chemistry (561), pp. 119830 |
|
| 28. | Fetal hematological phenotypes of various hemoglobinopathies and demonstration of embryonic hemoglobins on capillary electrophoresis: a large cohort data from prenatal screening program. | Singha, K Yamsri, S Chaibunruang, A Srivorakun, H Pansuwan, A Sanchaisuriya, K Fucharoen, G Fucharoen, S |
2025 |
Diagnosis (Berlin, Germany) 3 (12), pp. 441-451 |
|
| 29. | Multiplex recombinase polymerase amplification (RPA) assay for carrier detection and prenatal diagnosis of α-thalassemia (SEA and THAI deletions). | Sitthisophonkamjorn, Y Prommetta, S Chaibunruang, A Srivorakun, H Fucharoen, S Yamsri, S |
2025 |
Scandinavian journal of clinical and laboratory investigation (), pp. 1-7 |
| Title | Authors | Year | Journal title | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | 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 |
15 | 0 | 0 | 0 | 0 | 0 | 15 | |
| 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 |
15 | 0 | 0 | 0 | 0 | 0 | 15 | |
| 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 |
2 | 0 | 0 | 0 | 0 | 0 | 2 | |
| 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 |
6 | 0 | 0 | 0 | 0 | 0 | 6 | |
| 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 3.0 (43.0), pp. 500.0-505.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 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 Supan Fucharoen |
2021 |
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION 7.0 (81.0), pp. 557.0-563.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| Title | Authors | Year | Journal title |
|---|
| ชื่อโครงการ | Authors | ประเภทโครงการ | ปีงบประมาณ | ทุนวิจับ |
|---|