Wanicha Tepakhan

A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression

Diyu Chen, Yangjin Zuo, Xinhua Zhang et al. · The American Journal of Human Genetics · 2017 · 42 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7

Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome

Wanicha Tepakhan, Supawadee Yamsri, Goonnapa Fucharoen et al. · Annals of Hematology · 2015 · 21 citations

Hemoglobins F, Genetic Disorder, Genetics +9

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 et al. · Blood Cells Molecules and Diseases · 2016 · 18 citations

Transcriptional Regulation, Developmental Biology, Genetic Disorder +10

Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion

Wittaya Jomoui, Sitthichai Panyasai, Pornpun Sripornsawan et al. · Scientific Reports · 2023 · 15 citations · Full text

Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand

Wittaya Jomoui, Wanicha Tepakhan, Surada Satthakarn et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 2020 · 13 citations