Hataichanok Srivorakun

Khon Kaen, Thailand

Last Updated: 09/26/2026

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Found 29 publications

Elevated Hemoglobin A2: A Molecular Revisited, and Implications to β-Thalassemia Screening.

Elevated Hemoglobin A2: A Molecular Revisited, and Implications to β-Thalassemia Screening.

Journal: Journal of clinical laboratory analysis

Published: March 13, 2026

Molecular and hematological characterization of thalassemia and hemoglobinopathies among pediatric patients in northern Lao People's Democratic Republic.

Molecular and hematological characterization of thalassemia and hemoglobinopathies among pediatric patients in northern Lao People's Democratic Republic.

Journal: Scientific reports

Published: January 13, 2026

Common hemoglobin variants affecting the diagnosis of β-thalassemia: A large cohort data at a single center.

Common hemoglobin variants affecting the diagnosis of β-thalassemia: A large cohort data at a single center.

Journal: PloS one

Published: December 16, 2025

Direct PCR-Based VNTR Analysis of TPO Intron 10 for Rapid Detection of Maternal Cell Contamination in Prenatal Diagnosis.

Direct PCR-Based VNTR Analysis of TPO Intron 10 for Rapid Detection of Maternal Cell Contamination in Prenatal Diagnosis.

Journal: Clinical and translational science

Published: September 16, 2025

Hemoglobinopathies and iron deficiency among Northeast-Thai blood donors deferred for low hemoglobin.

Hemoglobinopathies and iron deficiency among Northeast-Thai blood donors deferred for low hemoglobin.

Journal: Scientific reports

Published: April 01, 2025

Multiplex recombinase polymerase amplification (RPA) assay for carrier detection and prenatal diagnosis of α0-thalassemia (SEA and THAI deletions).

Multiplex recombinase polymerase amplification (RPA) assay for carrier detection and prenatal diagnosis of α0-thalassemia (SEA and THAI deletions).

Journal: Scandinavian journal of clinical and laboratory investigation

Published: February 06, 2025

Fetal hematological phenotypes of various hemoglobinopathies and demonstration of embryonic hemoglobins on capillary electrophoresis: a large cohort data from prenatal screening program.

Fetal hematological phenotypes of various hemoglobinopathies and demonstration of embryonic hemoglobins on capillary electrophoresis: a large cohort data from prenatal screening program.

Journal: Diagnosis (Berlin, Germany)

Published: November 30, 2024

A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation.

A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: April 27, 2024

A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation.

A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: August 09, 2023

Anemia in an ethnic minority group in lower northern Thailand: A community-based study investigating the prevalence in relation to inherited hemoglobin disorders and iron deficiency.

Anemia in an ethnic minority group in lower northern Thailand: A community-based study investigating the prevalence in relation to inherited hemoglobin disorders and iron deficiency.

Journal: PloS one

Published: April 23, 2023

Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A2 levels or hemoglobin A2 variants: A single center experience.

Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A2 levels or hemoglobin A2 variants: A single center experience.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: April 04, 2023

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 with α-globin gene triplication.

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 with α-globin gene triplication.

Journal: PeerJ

Published: January 07, 2023

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Last Updated: 09/26/2026