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Wittaya Jomoui

Observed name: Jomoui, Wittaya
ORCID: 0000-0002-6035-3006
Observed ORCID: 0000-0002-6035-3006
OpenAlex ID: A5057995185
Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis
2015 · Wittaya Jomoui, Goonnapa Fucharoen, et al. · PLoS ONE · 41
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Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion
2023 · Wittaya Jomoui, Sitthichai Panyasai, et al. · Scientific Reports · 31
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Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis
2022 · Wittaya Jomoui, Hataichanok Srivorakun, et al. · PLoS ONE · 23
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Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand
2020 · Wittaya Jomoui, Wanicha Tepakhan, et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 19
Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart’s hydrops fetalis syndrome
2017 · Wittaya Jomoui, Goonnapa Fucharoen, et al. · Journal of Human Genetics · 18
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Molecular analysis of haemoglobin E in Southeast Asian populations
2017 · Wittaya Jomoui, Goonnapa Fucharoen, et al. · Annals of Human Biology · 14
Molecular Spectrum of β-Thalassemia Mutations in Central to Eastern Thailand
2021 · Prapaporn Panichchob, Pooncharus Iamdeelert, et al. · Hemoglobin · 12
Screening of (–SEA) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies
2016 · Wittaya Jomoui, Goonnapa Fucharoen, et al. · Journal of Clinical Pathology · 11
Rapid Molecular Detection for Differentiation of Homozygous HbE and ß0-Thalassemia/HbE in Samples Related With HbE >80% and Variable HbF Levels
2020 · Wanicha Tepakhan, Wittaya Jomoui · Laboratory Medicine · 9
Genetic Background Studies of Eight Common Beta Thalassemia Mutations in Thailand Using β-Globin Gene Haplotype and Phylogenetic Analysis
2022 · Rossarin Karnpean, Wanicha Tepakhan, et al. · Genes · 8
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Rapid molecular diagnostics of large deletional β0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes
2021 · Wanicha Tepakhan, Wittaya Jomoui · Heliyon · 8
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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: c.142G>A) in a Single Tube
2019 · Wittaya Jomoui, Prapaporn Panichchob, et al. · Hemoglobin · 7
Direct cord blood LAMP colorimetric phenol red assay for detecting α 0 -thalassemia (SEA deletion); the validation and post-natal screening in Thailand
2023 · Rossarin Karnpean, Amarin Narkwichean, et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 5
Molecular understanding of unusual HbE-β + -thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels
2023 · Wittaya Jomoui, Surada Satthakarn, et al. · Annals of Medicine · 5
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Characterization and identification of Prachinburi β0‐thalassemia: A novel‐60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state
2021 · Wittaya Jomoui, Wanicha Tepakhan · International Journal of Laboratory Hematology · 5
Retrospective study and implementation of a low-cost LAMP-turbidimetric assay for screening α0-thalassemia (SEA deletion): preventing and controlling Hb Bart’s hydrops fetalis syndrome in Thailand
2024 · Wittaya Jomoui, Kanokkorn Saknava, et al. · PeerJ · 4
Genetics background of β‐thalassemia (3.5 kb deletion) in Southern Thailand: Haplotype analysis using novel reverse dot blot hybridization
2021 · Wanicha Tepakhan, Korntip Srewaradachpisal, et al. · Annals of Human Genetics · 4
A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders
2019 · Wittaya Jomoui, Wanicha Tepakhan, et al. · Annals of Hematology · 4
Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand
2019 · Wittaya Jomoui, Wanicha Tepakhan, et al. · Hemoglobin · 3
Utilizing loop-mediated isothermal amplification (LAMP) for detecting hemoglobin Constant Spring and hemoglobin Pakse mutations amidst the high prevalence and genetic heterogeneity of thalassemia in Thailand
2025 · Kasama Wongprachum, Nichakan Thitipoomdecha, et al. · PeerJ · 2
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Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism
2025 · Chidchanok Mahabhol, Lalana Yothindamrongkul, et al. · Annals of Hematology · 2
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The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS)
2024 · Rossarin Karnpean, Wanicha Tepakhan, et al. · Hemoglobin · 2
Non-invasive Prenatal Testing for Hemoglobin Bart’s Hydrops Fetalis Syndrome (SEA Deletion) Using Cell-Free Fetal DNA in Maternal Plasma: Systematic Review and Meta-analysis
2018 · Wittaya Jomoui · International Journal of Human Genetics · 2
Assessment of factor structure of the Eating Attitude Test-26 (EAT-26) scale using data of young adults in the sociocultural context of Thailand
2025 · Kasama Wongprachum, Chaloemporn Namyota, et al. · Heliyon · 1
Development of LAMP-colorimetric assay for detecting hemoglobin Constant Spring and hemoglobin Pakse' v1
2025 · Wittaya Jomoui · 1
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Works count: 38
Citation count: 243
H-index: 9
I10-index: 8
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