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Kritsada Singha

Observed name: K. Singha
ORCID: 0000-0001-8716-5745
Observed ORCID: 0000-0001-8716-5745
OpenAlex ID: A5042956592
A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
2014 · Hataichanok Srivorakun, Kritsada Singha, et al. · PLoS ONE · 58
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A large cohort of β+-thalassemia in Thailand: Molecular, hematological and diagnostic considerations
2014 · Supawadee Yamsri, Kritsada Singha, et al. · Blood Cells Molecules and Diseases · 40
Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics
2019 · Thanyaornwanya Charoenwijitkul, Kritsada Singha, et al. · Clinical Biochemistry · 35
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Erythrocyte indices in a large cohort of β‐thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia
2019 · Kritsada Singha, Wachiraporn Taweenan, et al. · International Journal of Laboratory Hematology · 30
Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] withα0-Thalassemia: Molecular and Hematological Features and Differential Diagnosis
2012 · Kritsada Singha, Hataichanok Srivorakun, et al. · Hemoglobin · 20
A novel Aγδβ0-thalassemia caused by DNA deletion–inversion–insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization
2015 · Kritsada Singha, Goonnapa Fucharoen, et al. · Clinical Biochemistry · 18
δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia
2021 · Kritsada Singha, Goonnapa Fucharoen, et al. · Annals of Hematology · 11
EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin E-β0-thalassemia
2018 · Kritsada Singha, Goonnapa Fucharoen, et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 11
Co‐inheritance of α0‐thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications
2017 · K. Singha, H. Srivorakun, et al. · International Journal of Laboratory Hematology · 11
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
2013 · Kritsada Singha, Goonnapa Fucharoen, et al. · Clinical Biochemistry · 11
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
2022 · Kritsada Singha, Supawadee Yamsri, et al. · Orphanet Journal of Rare Diseases · 10
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Molecular basis of Hb H and AEBart’s diseases in the Lao People’s Democratic Republic
2019 · Kritsada Singha, Hataichanok Srivorakun, et al. · International Journal of Laboratory Hematology · 10
A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation
2024 · Kritsada Singha, Wanicha Tepakhan, et al. · Clinica Chimica Acta · 9
A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation
2023 · Kritsada Singha, Wanicha Tepakhan, et al. · Clinica Chimica Acta · 9
Five Hemoglobin Variants in a Double Heterozygote for α- and β-Globin Chain Defects
2013 · Kritsada Singha, Goonnapa Fucharoen, et al. · Acta Haematologica · 8
β‐Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program
2020 · Kritsada Singha, Attawut Chaibunruang, et al. · International Journal of Laboratory Hematology · 7
Molecular basis of a high Hb A2/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction withα-globin gene triplication
2023 · Chayada Soontornpanawet, Kritsada Singha, et al. · PeerJ · 6
Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia
2019 · Aye Chan Pyae, Hataichanok Srivorakun, et al. · Hemoglobin · 6
Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G>A;92+7A>G]): a novel form of Hb E-β-thalassaemia syndrome
2019 · Kritsada Singha, Goonnapa Fucharoen, et al. · Journal of Clinical Pathology · 6
Novel interactions of two α-Hb variants with SEA deletion α0-thalassemia: hematological and molecular analyses
2017 · Hataichanok Srivorakun, Kritsada Singha, et al. · Hematology · 6
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A spurious haemoglobin A 1c result associated with double heterozygote for haemoglobin Raleigh ( β 1[NA1]Val → Ala) and α + -thalassaemia
2012 · Kritsada Singha, Goonnapa Fucharoen, et al. · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 6
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Molecular basis of non-deletional HPFH in Thailand and identification of two novel mutations at the binding sites of CCAAT and GATA-1 transcription factors
2023 · Kritsada Singha, Anupong Pansuwan, et al. · Scientific Reports · 5
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Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A2 levels or hemoglobin A2 variants: A single center experience
2023 · Chulikon Hanart, Kritsada Singha, et al. · Clinica Chimica Acta · 5
Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program
2023 · Kritsada Singha, Supawadee Yamsri, et al. · PLoS ONE · 5
Molecular Characteristics of Hb New York [β113(G15)Val→Glu,HBB: c.341T>A] in Thailand
2018 · Attawut Chaibunruang, Kritsada Singha, et al. · Hemoglobin · 5
Works count: 44
Citation count: 372
H-index: 10
I10-index: 12
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