Wittaya Jomoui

13PUBLICATIONS
10CO-AUTHORS
HaematologyInfant and child healthAnthropological geneticsGenomicsGene mapping
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Publications (13)

|Aug 15, 2026
Simultaneous detection of thalassemia, hemoglobinopathies, and G6PD variants using long-read nanopore sequencing: genetic complexity and heterogeneity in Thailand.

|Jul 01, 2026
Enhancing Hemoglobin Bart's hydrops fetalis syndrome prevention: a single-tube multiplex real-time PCR assay for the comprehensive detection of four significant α0-thalassemia deletions (--SEA, --THAI, --CR, and --SA) found in Thailand.

|Mar 17, 2025
Rapid and Visual Molecular Detection of High Hb F Determinants; HPFH6, Asian Indian inv-del (Aγδβ)0-Thalassemia, and Thai del-inv-ins (Aγδβ)0-Thalassemia Using LAMP Colorimetric Phenol Red Assays.

Wittaya Jomoui, Wanicha Tepakhan

|Mar 06, 2025
Alpha-globin gene cluster haplotypes and D1S80, D17S5, and TPO VNTR polymorphisms among four ethnic populations from lower northeastern Thailand.

Sanita Singsanan, Wittaya Jomoui, Monpat Chamnanphon

|Nov 14, 2024
The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS).

Rossarin Karnpean, Wanicha Tepakhan, Kittiphoom Rungruang

|Oct 10, 2023
Molecular understanding of unusual HbE-β+-thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels.

Wittaya Jomoui, Surada Satthakarn, Sitthichai Panyasai

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Frequent Collaborators

3 joint publications

Wanicha Tepakhan

2 joint publications

Sitthichai Panyasai

2 joint publications

Supan Fucharoen

2 joint publications

Rossarin Karnpean