| Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families S Fucharoen, K Sanchaisuriya, G Fucharoen, S Panyasai, R Devenish, ... haematologica 88 (10), 1092-1098, 2003 | 116 | 2003 |
| A simplified screening for α-thalassemia 1 (SEA type) using a combination of a modified osmotic fragility test and a direct PCR on whole blood cell lysates S Panyasai, P Sringam, G Fucharoen, K Sanchaisuriya, S Fucharoen Acta haematologica 108 (2), 74-78, 2002 | 52 | 2002 |
| Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand S Panyasai, S Fucharoen, S Surapot, G Fucharoen, K Sanchaisuriya haematologica 89 (7), 777-781, 2004 | 43 | 2004 |
| Comparison Between Capillary Electrophoresis and High Performance Liquid Chromatography for Detection and Quantification of Hb Constant Spring [Hb CS; α142, Term→ Gln (TAA> C … J Waneesorn, S Panyasai, K Kongthai, P Singboottra, S Pornprasert Hemoglobin 35 (4), 338-345, 2011 | 26 | 2011 |
| Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening S Panyasai, G Fucharoen, S Fucharoen Clinica Chimica Acta 438, 226-230, 2015 | 20 | 2015 |
| Molecular confirmatory testing of hemoglobin Constant Spring by real‐time polymerase chain reaction SYBR Green1 with high‐resolution melting analysis S Panyasai, K Sukunthamala, S Pornprasert European journal of haematology 84 (6), 550-552, 2010 | 17 | 2010 |
| Hemoglobin variants in Northern Thailand: prevalence, heterogeneity and molecular characteristics S Panyasai, G Fucharoen, S Fucharoen Genetic Testing and Molecular Biomarkers 20 (1), 37-43, 2016 | 15 | 2016 |
| Quantification of hemoglobin Constant Spring in heterozygote and homozygote by a capillary electrophoresis method S Pornprasert, S Panyasai, J Waneesorn, K Kongthai, P Singboottra International Journal of Laboratory Hematology 34 (2), 143-147, 2012 | 15 | 2012 |
| Interference of hemoglobin Hope on β-thalassemia diagnosis by the capillary electrophoresis method S Panyasai, K Sukunthamala, K Jaiping, S Wongwiwatthananukit, ... American journal of clinical pathology 136 (1), 14-18, 2011 | 15 | 2011 |
| Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its Combinations in Patients also Carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in Northern … S Pornprasert, S Panyasai, K Treesuwan Hemoglobin 36 (5), 491-496, 2012 | 12 | 2012 |
| Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels S Satthakarn, S Panyasai, S Pornprasert Hemoglobin 44 (5), 349-353, 2020 | 11 | 2020 |
| Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand W Jomoui, W Tepakhan, S Satthakarn, S Panyasai Scandinavian Journal of Clinical and Laboratory Investigation 80 (7), 528-535, 2020 | 9 | 2020 |
| Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation ‐‐SEA/‐‐CR, a novel α0‐thalassemia deletion. C Ruengdit, S Panyasai, N Kunyanone, W Phornsiricharoenphant, ... International Journal of Laboratory Hematology 42 (3), 2020 | 9 | 2020 |
| Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion W Jomoui, S Panyasai, P Sripornsawan, W Tepakhan Scientific Reports 13 (1), 9850, 2023 | 7 | 2023 |
| Hemoglobin Q-Thailand and its combinations with other forms of thalassemia or hemoglobinopathies in northern Thailand S Panyasai, S Pornprasert Clin Lab 60 (7), 1099-1103, 2014 | 7 | 2014 |
| Compound heterozygote state for GγAγ(δβ)°‐thalassemia and hereditary persistence of fetal hemoglobin S Fucharoen, S Panyasai, S Surapot, G Fucharoen, K Sanchaisuriya American journal of hematology 80 (2), 119-123, 2005 | 7 | 2005 |
| Coinheritance of Hb A2-Melbourne (HBD: c. 130G> A) and Hb E (HBB: c. 79G> A) in Laos and simultaneous high resolution melt detection of Hb A2-Melbourne and Hb A2-Lampang (HBD … W Jomoui, P Panichchob, P Rujirachaivej, S Panyasai, W Tepakhan Hemoglobin 43 (3), 214-217, 2019 | 6 | 2019 |
| Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA2 Levels on Capillary Electrophoresis S Panyasai, S Sakkhachornphop, S Pornprasert Indian Journal of Hematology and Blood Transfusion 34, 110-114, 2018 | 6 | 2018 |
| Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart’s on Capillary Electrophoresis K Khongthai, C Ruengdit, S Panyasai, S Pornprasert Hemoglobin 43 (4-5), 245-248, 2019 | 5 | 2019 |
| Coinheritance of hemoglobin D-Punjab and β0-thalassemia 3.4 kb deletion in a Thai girl S Panyasai, S Rahad, S Pornprasert Asian journal of transfusion science 11 (2), 199-202, 2017 | 5 | 2017 |
