| Title | Author | Year | SCOPUS | PUBMED | ISI | TCI | |
|---|---|---|---|---|---|---|---|
| 1. | 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 | ||||
| 2. | 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.P. |
2006 | ||||
| 3. | 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 | ||||
| 4. | 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 | ||||
| 5. | 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 | ||||
| 6. | 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 | ||||
| 7. | 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 | ||||
| 8. | 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 | ||||
| 9. | Thalassemia and iron deficiency in a group of northeast Thai school children: Relationship to the occurrence of anemia | Nichathorn Panomai Kanokwan Sanchaisuriya Supawadee Yamsri Pattara Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen Frank P. Schelp |
2010 | ||||
| 10. | 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 | ||||
| 11. | 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 | ||||
| 12. | 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 | ||||
| 13. | Genetic origin and interaction of the Filipino β 0- thalassemia with Hb e and α-thalassemia in a Thai family | Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2012 | ||||
| 14. | 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 | ||||
| 15. | Non-invasive prenatal diagnosis of beta-thalassemia and sickle-cell disease using pyrophosphorolysis-activated polymerization and melting curve analysis. | Marion Phylipsen Supawadee Yamsri Emmely E. Treffers Diahann T. S. L. Jansen Warsha A. Kanhai Elles M. J. Boon Piero C. Giordano Supan Fucharoen Egbert Bakker Cornelis L. Harteveld |
2012 | ||||
| 16. | 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 | ||||
| 17. | 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 | ||||
| 18. | 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 | ||||
| 19. | VARIABILITY OF HEMOGLOBIN F EXPRESSION IN HEMOGLOBIN EE DISEASE: HEMATOLOGICAL AND MOLECULAR ANALYSIS | Yamsri, S. Fucharoen, G. Sanchaisuriya, K. Fucharoen, S.P. |
2014 | ||||
| 20. | 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 | ||||
| 21. | 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 | ||||
| 22. | Krüppel-like factor 1 mutations and expression of hemoglobins F and A |
Tepakhan, W. Yamsri, S. Fucharoen, G. Sanchaisuriya, K. Fucharoen, S.P. |
2015 | ||||
| 23. | 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 | ||||
| 24. | 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 | ||||
| 25. | Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-beta-Thalassemia in Northeast Thailand | Yamsri, S Pakdee, N Fucharoen, G Sanchaisuriya, K Fucharoen, S |
2016 | ||||
| 26. | 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 | ||||
| 27. | 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 | ||||
| 28. | 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 | ||||
| 29. | 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 | ||||
| 30. | INITIATION OF SCREENING PROGRAM FOR THALASSEMIA IN A GROUP OF REPRODUCTIVE- AGE WOMEN OF ETHNIC MINORITIES IN NORTHERN VIETNAM | Hanh Hong Hoa Kanokwan Sanchaisuriya Jutatip Jamnok Supawadee Yamsri Vinh Hac Van Pattara Sanchaisuriya |
2018 | ||||
| 31. | 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 | ||||
| 32. | Whole Blood PCR for Rapid Screening of alpha(0)-Thalassemia | Phongsathorn Wichian Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2018 | ||||
| 33. | Whole blood PCR for rapid screening of α0-thalassemia | Yamsri, S. Sanchaisuriya, K. Fucharoen, G. Fucharoen, S.P. |
2018 | ||||
| 34. | Whole Blood PCR for Rapid Screening of α-Thalassemia. | Wichian, P Yamsri, S Sanchaisuriya, K Fucharoen, G Fucharoen, S |
2018 | ||||
| 35. | WHOLE BLOOD PCR KIT FOR RAPID IDENTIFICATION OF alpha(0)-THALASSEMIA | Supawadee Yamsri Phongsathorn Wichian Rossarin Karnpean Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2018 | ||||
| 36. | Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-beta-Thalassemia Disease without alpha-Thalassemia | Yamsri, S. Teawtrakul, N. Fucharoen, G. Sanchaisuriya, K. Fucharoen, S.P. |
2019 | ||||
| 37. | 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 | ||||
| 38. | 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 | ||||
| 39. | Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-beta(0)-Thalassemia Diseases | Phongsathorn Wichian Supawadee Yamsri Kanokwan Sanchaisuriya Supan Fucharoen |
2021 | ||||
| 40. | Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-β 0-Thalassemia Diseases | Wichian, P Yamsri, S Sanchaisuriya, K Fucharoen, S |
2021 | ||||
| 41. | 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 | ||||
| 42. | Generation of a single-tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies | Anupong Pansuwan Duangrudee Changtrakul Attawut Chaibunruang Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2021 | ||||
| 43. | JAK2V617F mutation in patients with β-thalassemia disease: prevalence and clinical characteristics | Nattiya Teawtrakul Siriyakorn Chansai Supawadee Yamsri Piti Ungarreevittaya |
2021 | ||||
| 44. | Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Females from Previously Malaria Endemic Regions in Northeastern Thailand and Identification of a Novel G6PD Variant | Dechyotin, S Sakunthai, K Khemtonglang, N Yamsri, S Sanchaisuriya, K Kitcharoen, K Kitcharoen, S |
2021 | ||||
| 45. | Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand | Anupong Pansuwan Supawadee Yamsri Duangrudee Changtrakul Goonnapa Fucharoen Supan Fucharoen |
2021 | ||||
| 46. | Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand. | Pansuwan, A. Yamsri, S. Changtrakul, D. Fucharoen, G. Fucharoen, S.P. |
2021 | ||||
| 47. | Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematologic Analyses | Supawadee Yamsri Watcharaphong Kawon Amara Duereh Goonnapa Fucharoen Supan Fucharoen |
2021 | ||||
| 48. | 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 | ||||
| 49. | 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 | ||||
| 50. | Five Variable Number of Tandem Repeats Loci (D17S5, APOB, TPO Intron 10, IL-1α Intron 6, and CIAS1) in Thais and Application in the Prenatal Diagnostic Laboratory. | Singsanan, S. Yamsri, S. Pangjit, K. Saenwang, P. Karnpean, R. Fucharoen, S. |
2022 | ||||
| 51. | FLT3 Gene Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand. | Ei Ei Aung, N Yamsri, S Teawtrakul, N Kamsaen, P Fucharoen, S |
2022 | ||||
| 52. | Generation of a single-tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies. | Pansuwan, A. Changtrakul, D. Chaibunruang, A. Yamsri, S. Sanchaisuriya, K. Fucharoen, G. Fucharoen, S.P. |
2022 | ||||
| 53. | Phosphatidylserine-exposed red blood cells and ineffective erythropoiesis biomarkers in patients with thalassemia. | Chansai, S Yamsri, S Fucharoen, S Fucharoen, G Teawtrakul, N |
2022 | ||||
| 54. | The Correlation Between Ineffective Erythropoiesis Biomarkers and Development of Extramedullary Hematopoiesis in Patients with Thalassemia. | Chansai, S. Yamsri, S. Fucharoen, S. Fucharoen, G. Teawtrakul, N. |
2022 | ||||
| 55. | 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 | ||||
| 56. | 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 | ||||
| 57. | The association of growth differentiation factor-15 levels and osteoporosis in patients with thalassemia. | Teawtrakul, N Chansai, S Yamsri, S Chansung, K Wanitpongpun, C Lanamtieng, T Phiphitaporn, P Fucharoen, S Pongchaiyakul, C |
2023 | ||||
| 58. | 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 | ||||
| 59. | 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 | ||||
| 60. | 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 | ||||
| 61. | 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 | ||||
| 62. | Prenatal diagnostic errors in hemoglobin Bart's hydrops fetalis caused by rare genetic interactions of α-thalassemia. | Singha, K Yamsri, S Sanchaisuriya, K Fucharoen, G Fucharoen, S |
2025 | Count | 32 | 39 | 37 | 0 |
| Title | Authors | Year | Publication name | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | Total | ||||||
| 1. | 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 |
||||||||
| 2. | 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 |
||||||||
| 3. | 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 |
||||||||
| 4. | 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 |
||||||||
| 5. | 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 |
||||||||
| 6. | 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 |
||||||||
| 7. | Non-invasive prenatal diagnosis of beta-thalassemia and sickle-cell disease using pyrophosphorolysis-activated polymerization and melting curve analysis | Phylipsen, M. Yamsri, S. Treffers, E.E. Kanhai, W.A. Boon, E.M.J. Fucharoen, S.P. |
2012 |
Prenatal Diagnosis 6 (32), pp. 578-587 |
||||||||
| 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. | 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 |
||||||||
| 10. | 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 |
||||||||
| 11. | 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 |
||||||||
| 12. | 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. |
||||||||
| 13. | 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 |
||||||||
| 14. | 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 |
||||||||
| 15. | 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 |
||||||||
| 16. | 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 |
||||||||
| 17. | 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 |
||||||||
| 18. | 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. |
||||||||
| 19. | 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 |
||||||||
| 20. | Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-β 0-Thalassemia Diseases | Wichian, P. Yamsri, S. Sanchaisuriya, K. Fucharoen, S.P. |
2021 |
Laboratory medicine 5 (52), pp. 460-468 |
||||||||
| 21. | 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 |
||||||||
| 22. | 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 |
||||||||
| 23. | JAK2V617F mutation in patients with β-thalassemia disease: prevalence and clinical characteristics | Teawtrakul, N. Chansai, S. Yamsri, S. Ungarreevittaya, P. |
2021 |
Annals of Hematology 11 (100), pp. 2863-2865 |
||||||||
| 24. | Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Females from Previously Malaria Endemic Regions in Northeastern Thailand and Identification of a Novel G6PD Variant | Dechyotin, S. Khemtonglang, N. Yamsri, S. Sanchaisuriya, K. Kitcharoen, K. Kitcharoen, S. |
2021 |
Mediterranean Journal of Hematology and Infectious Diseases 1 (13), pp. |
||||||||
| 25. | Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand | Pansuwan, A. Yamsri, S. Changtrakul, D. Fucharoen, G. Fucharoen, S.P. |
2021 |
International Journal of Laboratory Hematology 4 (43), pp. 845-852 |
||||||||
| 26. | Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematologic Analyses | Yamsri, S. Fucharoen, G. Fucharoen, S.P. |
2021 |
Journal of Pediatric Hematology/Oncology 3 (43), pp. e341-e345 |
||||||||
| 27. | 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. |
||||||||
| 28. | Five Variable Number of Tandem Repeats Loci (D17S5, APOB, TPO Intron 10, IL-1α Intron 6, and CIAS1) in Thais and Application in the Prenatal Diagnostic Laboratory | Singsanan, S. Yamsri, S. Pangjit, K. Saenwang, P. Karnpean, R. Fucharoen, S. |
2022 |
Genetic Testing and Molecular Biomarkers 6 (26), pp. 324-330 |
||||||||
| 29. | Generation of a single-tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies | Pansuwan, A. Changtrakul, D. Chaibunruang, A. Yamsri, S. Sanchaisuriya, K. Fucharoen, G. Fucharoen, S.P. |
2022 |
International Journal of Laboratory Hematology 3 (44), pp. 666-672 |
||||||||
| 30. | The Correlation Between Ineffective Erythropoiesis Biomarkers and Development of Extramedullary Hematopoiesis in Patients with Thalassemia | Chansai, S. Yamsri, S. Fucharoen, S. Fucharoen, G. Teawtrakul, N. |
2022 |
Mediterranean Journal of Hematology and Infectious Diseases 1 (14), pp. |
||||||||
| 31. | 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. |
||||||||
| 32. | 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. | 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 |
|
| 2. | 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 |
|
| 3. | 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 |
|
| 4. | 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 |
|
| 5. | 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 |
|
| 6. | Non-invasive prenatal diagnosis of beta-thalassemia and sickle-cell disease using pyrophosphorolysis-activated polymerization and melting curve analysis. | Phylipsen, M Yamsri, S Treffers, EE Jansen, DT Kanhai, WA Boon, EM Giordano, PC Fucharoen, S Bakker, E Harteveld, CL |
2012 |
Prenatal diagnosis 6 (32), pp. 578-87 |
|
| 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. | 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 |
|
| 9. | 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 |
|
| 10. | 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 |
|
| 11. | 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 |
|
| 12. | 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 |
|
| 13. | 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 |
|
| 14. | 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 |
|
| 15. | 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 |
|
| 16. | 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 |
|
| 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. | Jomoui, W Tepakhan, W Yamsri, S Srivorakun, H Fucharoen, G Fucharoen, S |
2020 |
Annals of hematology 1 (99), pp. 23-29 |
|
| 18. | 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 |
|
| 19. | Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematologic Analyses. | Yamsri, S Kawon, W Duereh, A Fucharoen, G Fucharoen, S |
2021 |
Journal of pediatric hematology/oncology 3 (43), pp. e341-e345 |
|
| 20. | Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-β 0-Thalassemia Diseases. | Wichian, P Yamsri, S Sanchaisuriya, K Fucharoen, S |
2021 |
Laboratory medicine 5 (52), pp. 460-468 |
|
| 21. | Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand. | Pansuwan, A Yamsri, S Changtrakul, D Fucharoen, G Fucharoen, S |
2021 |
International journal of laboratory hematology 4 (43), pp. 845-852 |
|
| 22. | 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 |
|
| 23. | Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Females from Previously Malaria Endemic Regions in Northeastern Thailand and Identification of a Novel G6PD Variant. | Dechyotin, S Sakunthai, K Khemtonglang, N Yamsri, S Sanchaisuriya, K Kitcharoen, K Kitcharoen, S |
2021 |
Mediterranean journal of hematology and infectious diseases 1 (13), pp. e2021029 |
|
| 24. | JAK2V617F mutation in patients with β-thalassemia disease: prevalence and clinical characteristics. | Teawtrakul, N Chansai, S Yamsri, S Ungarreevittaya, P |
2021 |
Annals of hematology 11 (100), pp. 2863-2865 |
|
| 25. | 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 |
|
| 26. | 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 |
|
| 27. | Generation of a single-tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies. | Pansuwan, A Changtrakul, D Chaibunruang, A Yamsri, S Sanchaisuriya, K Fucharoen, G Fucharoen, S |
2022 |
International journal of laboratory hematology 3 (44), pp. 666-672 |
|
| 28. | Five Variable Number of Tandem Repeats Loci (D17S5, APOB, TPO Intron 10, IL-1α Intron 6, and CIAS1) in Thais and Application in the Prenatal Diagnostic Laboratory. | Singsanan, S Yamsri, S Pangjit, K Saenwang, P Karnpean, R Fucharoen, S |
2022 |
Genetic testing and molecular biomarkers 6 (26), pp. 324-330 |
|
| 29. | The Correlation Between Ineffective Erythropoiesis Biomarkers and Development of Extramedullary Hematopoiesis in Patients with Thalassemia. | Chansai, S Yamsri, S Fucharoen, S Fucharoen, G Teawtrakul, N |
2022 |
Mediterranean journal of hematology and infectious diseases 1 (14), pp. e2022052 |
|
| 30. | Phosphatidylserine-exposed red blood cells and ineffective erythropoiesis biomarkers in patients with thalassemia. | Chansai, S Yamsri, S Fucharoen, S Fucharoen, G Teawtrakul, N |
2022 |
American journal of translational research 7 (14), pp. 4743-4756 |
|
| 31. | FLT3 Gene Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand. | Ei Ei Aung, N Yamsri, S Teawtrakul, N Kamsaen, P Fucharoen, S |
2022 |
Medical science monitor basic research (28), pp. e937446 |
|
| 32. | 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 |
|
| 33. | 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 |
|
| 34. | The association of growth differentiation factor-15 levels and osteoporosis in patients with thalassemia. | Teawtrakul, N Chansai, S Yamsri, S Chansung, K Wanitpongpun, C Lanamtieng, T Phiphitaporn, P Fucharoen, S Pongchaiyakul, C |
2023 |
The American journal of the medical sciences 2 (366), pp. 96-101 |
|
| 35. | 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 |
|
| 36. | 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 |
|
| 37. | Prenatal diagnostic errors in hemoglobin Bart's hydrops fetalis caused by rare genetic interactions of α-thalassemia. | Singha, K Yamsri, S Sanchaisuriya, K Fucharoen, G Fucharoen, S |
2025 |
Diagnosis (Berlin, Germany) 2 (12), pp. 256-261 |
|
| 38. | 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 |
|
| 39. | 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 |
| Title | Authors | Year | Journal title | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | Total | ||||||
| 1. | 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 | |
| 2. | 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 | |
| 3. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (30.0), pp. 136.0-136.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 4. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (30.0), pp. 126.0-126.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 5. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (30.0), pp. 135.0-135.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 6. | 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 |
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (94.0), pp. 516.0-516.0 |
2 | 0 | 0 | 0 | 0 | 0 | 2 | |
| 7. | Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center | Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Nattaya Sae-ung Thawalwong Ratanasiri Supan Fucharoen |
2010 |
PRENATAL DIAGNOSIS 6.0 (30.0), pp. 540.0-546.0 |
81 | 0 | 0 | 0 | 0 | 0 | 81 | |
| 8. | Thalassemia and iron deficiency in a group of northeast Thai school children: relationship to the occurrence of anemia | Nichathorn Panomai Kanokwan Sanchaisuriya Supawadee Yamsri Pattara Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen Frank P. Schelp |
2010 |
EUROPEAN JOURNAL OF PEDIATRICS 11.0 (169.0), pp. 1317.0-1322.0 |
18 | 0 | 0 | 0 | 0 | 0 | 18 | |
| 9. | Genotype and phenotype characterizations in a large cohort of beta-thalassemia heterozygote with different forms of alpha-thalassemia in northeast Thailand | Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Nattaya Sae-ung Supan Fucharoen |
2011 |
BLOOD CELLS MOLECULES AND DISEASES 2.0 (47.0), pp. 120.0-124.0 |
49 | 0 | 0 | 0 | 0 | 0 | 49 | |
| 10. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (34.0), pp. 149.0-149.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 11. | Genetic origin and interaction of the Filipino beta(0)-thalassemia with Hb E and alpha-thalassemia in a Thai family | Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2012 |
TRANSLATIONAL RESEARCH 6.0 (159.0), pp. 473.0-476.0 |
7 | 0 | 0 | 0 | 0 | 0 | 7 | |
| 12. | Non-invasive prenatal diagnosis of beta-thalassemia and sickle-cell disease using pyrophosphorolysis-activated polymerization and melting curve analysis | Marion Phylipsen Supawadee Yamsri Emmely E. Treffers Diahann T. S. L. Jansen Warsha A. Kanhai Elles M. J. Boon Piero C. Giordano Supan Fucharoen Egbert Bakker Cornelis L. Harteveld |
2012 |
PRENATAL DIAGNOSIS 6.0 (32.0), pp. 578.0-587.0 |
45 | 0 | 0 | 0 | 0 | 0 | 45 | |
| 13. | 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 | |
| 14. | Molecular and hematological studies in a large cohort of alpha(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 |
BLOOD CELLS MOLECULES AND DISEASES 2.0 (51.0), pp. 89.0-93.0 |
20 | 0 | 0 | 0 | 0 | 0 | 20 | |
| 15. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (36.0), pp. 122.0-122.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 16. | 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 |
BLOOD CELLS MOLECULES AND DISEASES 1-2 (53.0), pp. 11.0-15.0 |
28 | 0 | 0 | 0 | 0 | 0 | 28 | |
| 17. | A large cohort of beta(+)-thalassemia in Thailand: Molecular, hematological and diagnostic considerations | Supawadee Yamsri Kritsada Singha Thanet Prajantasen Wachiraporn Taweenan Goonnapa Fucharoen Kanokwan Sanchaisuriya Supan Fucharoen |
2015 |
BLOOD CELLS MOLECULES AND DISEASES 2.0 (54.0), pp. 164.0-169.0 |
27 | 0 | 0 | 0 | 0 | 0 | 27 | |
| 18. | 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 |
ANNALS OF HEMATOLOGY 7.0 (94.0), pp. 1093.0-1098.0 |
30 | 0 | 0 | 0 | 0 | 0 | 30 | |
| 19. | 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 |
INTERNATIONAL JOURNAL OF HUMAN GENETICS 4.0 (15.0), pp. 191.0-198.0 |
3 | 0 | 0 | 0 | 0 | 0 | 3 | |
| 20. | Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-beta-Thalassemia in Northeast Thailand | Supawadee Yamsri Naruwat Pakdee Goonnapa Fucharoen Kanokwan Sanchaisuriya Supan Fucharoen |
2016 |
ACTA HAEMATOLOGICA 4.0 (136.0), pp. 233.0-239.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 21. | Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-beta-Thalassemia in Northeast Thailand | Supawadee Yamsri Naruwat Pakdee Goonnapa Fucharoen Kanokwan Sanchaisuriya Supan Fucharoen |
2016 |
ACTA HAEMATOLOGICA 4.0 (136.0), pp. 233.0-239.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 22. | Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder | Wanicha Tepakhan Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Xiangmin Xu Supan Fucharoen |
2016 |
BLOOD CELLS MOLECULES AND DISEASES (59.0), pp. 85.0-91.0 |
18 | 0 | 0 | 0 | 0 | 0 | 18 | |
| 23. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (39.0), pp. 36.0-36.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 24. | Evaluation of staff performance and interpretation of the screening program for prevention of thalassemia | Simaporn Prommetta Kanokwan Sanchaisuriya Goonnapa Fucharoen Supawadee Yamsri Attawut Chaiboonroeng Supan Fucharoen |
2017 |
BIOCHEMIA MEDICA 2.0 (27.0), pp. 387.0-397.0 |
5 | 0 | 0 | 0 | 0 | 0 | 5 | |
| 25. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (40.0), pp. 62.0-62.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 26. | INITIATION OF SCREENING PROGRAM FOR THALASSEMIA IN A GROUP OF REPRODUCTIVE- AGE WOMEN OF ETHNIC MINORITIES IN NORTHERN VIETNAM | Hanh Hong Hoa Kanokwan Sanchaisuriya Jutatip Jamnok Supawadee Yamsri Vinh Hac Van Pattara Sanchaisuriya |
2018 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (40.0), pp. 58.0-58.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 27. | 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 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (40.0), pp. 157.0-157.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 28. | Whole Blood PCR for Rapid Screening of alpha(0)-Thalassemia | Phongsathorn Wichian Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2018 |
ANNALS OF CLINICAL AND LABORATORY SCIENCE 2.0 (48.0), pp. 231.0-235.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 29. | WHOLE BLOOD PCR KIT FOR RAPID IDENTIFICATION OF alpha(0)-THALASSEMIA | Supawadee Yamsri Phongsathorn Wichian Rossarin Karnpean Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2018 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (40.0), pp. 161.0-161.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 30. | Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-beta-Thalassemia Disease without alpha-Thalassemia | Paramee Phanrahan Supawadee Yamsri Nattiya Teawtrakul Goonnapa Fucharocn Kanolm An Sanchaisuriya Supan Fucharoen |
2019 |
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES (11.0), pp. |
10 | 0 | 0 | 0 | 0 | 0 | 10 | |
| 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 |
ANNALS OF HEMATOLOGY 1.0 (99.0), pp. 23.0-29.0 |
1 | 0 | 0 | 0 | 0 | 0 | 1 | |
| 32. | 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 | |
| 33. | Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-beta(0)-Thalassemia Diseases | Phongsathorn Wichian Supawadee Yamsri Kanokwan Sanchaisuriya Supan Fucharoen |
2021 |
LABORATORY MEDICINE 5.0 (52.0), pp. 460.0-468.0 |
1 | 0 | 0 | 0 | 0 | 0 | 1 | |
| 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 |
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION 7.0 (81.0), pp. 557.0-563.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 35. | Generation of a single-tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies | Anupong Pansuwan Duangrudee Changtrakul Attawut Chaibunruang Supawadee Yamsri Kanokwan Sanchaisuriya Goonnapa Fucharoen Supan Fucharoen |
2021 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY (), pp. |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 36. | JAK2V617F mutation in patients with beta-thalassemia disease: prevalence and clinical characteristics | Nattiya Teawtrakul Siriyakorn Chansai Supawadee Yamsri Piti Ungarreevittaya |
2021 |
ANNALS OF HEMATOLOGY 11.0 (100.0), pp. 2863.0-2865.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 37. | Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Females from Previously Malaria Endemic Regions in Northeastern Thailand and Identification of a Novel G6PD Variant | Sumalai Dechyotin Kittipong Sakunthai Noppmats Khemtonglang Supawadee Yamsri Kanokwan Sanchaisuriya Kriengkrai Kitcharoen Suttiphan Kitcharoen |
2021 |
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES (13.0), pp. |
2 | 0 | 0 | 0 | 0 | 0 | 2 | |
| 38. | Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand | Anupong Pansuwan Supawadee Yamsri Duangrudee Changtrakul Goonnapa Fucharoen Supan Fucharoen |
2021 |
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY 4.0 (43.0), pp. 845.0-852.0 |
1 | 0 | 0 | 0 | 0 | 0 | 1 | |
| 39. | Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematologic Analyses | Supawadee Yamsri Watcharaphong Kawon Amara Duereh Goonnapa Fucharoen Supan Fucharoen |
2021 |
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY 3.0 (43.0), pp. E341-E345 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
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