| A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration H Srivorakun, K Singha, G Fucharoen, K Sanchaisuriya, S Fucharoen PLoS One 9 (9), e108365, 2014 | 45 | 2014 |
| A large cohort of β+-thalassemia in Thailand: Molecular, hematological and diagnostic considerations S Yamsri, K Singha, T Prajantasen, W Taweenan, G Fucharoen, ... Blood Cells, Molecules, and Diseases 54 (2), 164-169, 2015 | 36 | 2015 |
| Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics T Charoenwijitkul, K Singha, G Fucharoen, K Sanchaisuriya, ... Clinical Biochemistry 71, 31-37, 2019 | 26 | 2019 |
| Erythrocyte indices in a large cohort of β‐thalassemia carrier: implication for population screening in an area with high prevalence and heterogeneity of thalassemia K Singha, W Taweenan, G Fucharoen, S Fucharoen International journal of laboratory hematology 41 (4), 513-518, 2019 | 26 | 2019 |
| A novel Aγδβ0-thalassemia caused by DNA deletion–inversion–insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological … K Singha, G Fucharoen, A Hama, S Fucharoen Clinical Biochemistry 48 (10-11), 703-708, 2015 | 16 | 2015 |
| Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α0-Thalassemia: Molecular and Hematological Features and … K Singha, H Srivorakun, G Fucharoen, Y Changtrakul, P Komwilaisak, ... Hemoglobin 37 (1), 37-47, 2013 | 14 | 2013 |
| Molecular and hematological characteristics of a novel form of α-globin gene triplication: the hemoglobin St. Luke's-Thailand [α95 (G2) Pro→ Arg] or Hb St. Luke's [A2] HBA2 K Singha, G Fucharoen, A Jetsrisuparb, S Fucharoen Clinical Biochemistry 46 (7-8), 675-680, 2013 | 12 | 2013 |
| Co‐inheritance of α0‐thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications K Singha, H Srivorakun, G Fucharoen, S Fucharoen International Journal of Laboratory Hematology 39 (5), 508-512, 2017 | 11 | 2017 |
| EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin E-β0-thalassemia K Singha, G Fucharoen, K Sanchaisuriya, S Fucharoen Clinical Chemistry and Laboratory Medicine (CCLM) 56 (9), 1507-1513, 2018 | 10 | 2018 |
| Molecular basis of Hb H and AEBart’s diseases in the Lao People’s Democratic Republic K Singha, H Srivorakun, G Fucharoen, S Fucharoen International Journal of Laboratory Hematology 42 (1), 23-27, 2020 | 8 | 2020 |
| δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia K Singha, G Fucharoen, S Fucharoen Annals of Hematology 100, 1953-1963, 2021 | 7 | 2021 |
| Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand A Chaibunruang, K Singha, H Srivorakun, G Fucharoen, S Fucharoen Hemoglobin 42 (1), 11-15, 2018 | 6 | 2018 |
| Five hemoglobin variants in a double heterozygote for α-and β-globin chain defects K Singha, G Fucharoen, S Fucharoen Acta Haematologica 131 (2), 71-75, 2014 | 6 | 2014 |
| A spurious haemoglobin A1c result associated with double heterozygote for haemoglobin Raleigh (β1[NA1]Val → Ala) and α+-thalassaemia K Singha, G Fucharoen, A Chaibunruang, P Netnee, S Fucharoen Annals of Clinical Biochemistry 49 (5), 445-449, 2012 | 6 | 2012 |
| 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 … K Singha, S Yamsri, A Chaibunruang, H Srivorakun, K Sanchaisuriya, ... Orphanet Journal of Rare Diseases 17 (1), 45, 2022 | 4 | 2022 |
| Novel interactions of two α-Hb variants with SEA deletion α0-thalassemia: hematological and molecular analyses H Srivorakun, K Singha, G Fucharoen, S Fucharoen Hematology 23 (3), 187-191, 2018 | 4 | 2018 |
| Molecular basis of a high Hb A2/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel … C Soontornpanawet, K Singha, H Srivorakun, W Tepakhan, G Fucharoen, ... PeerJ 11, e15308, 2023 | 3 | 2023 |
| Genetic and non-genetic factors affecting hemoglobin A2 expression in a large cohort of Thai individuals: implication for population screening for thalassemia K Singha, K Sanchaisuriya, G Fucharoen, S Fucharoen American Journal of Translational Research 13 (10), 11632, 2021 | 3 | 2021 |
| Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia AC Pyae, H Srivorakun, A Chaibunruang, K Singha, K Tomanakarn, ... Hemoglobin 43 (4-5), 254-257, 2019 | 3 | 2019 |
| Molecular characterisation of haemoglobin E-Udon Thani (HBB: c.[79G> A; 92+ 7A> G]): a novel form of Hb E-β-thalassaemia syndrome K Singha, G Fucharoen, S Fucharoen Journal of Clinical Pathology 72 (4), 322-324, 2019 | 3 | 2019 |
