Kanokwan Sanchaisuriya

Khon Kaen, Thailand

Last Updated: 09/26/2026

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Found 53 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

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

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

Prenatal diagnostic errors in hemoglobin Bart's hydrops fetalis caused by rare genetic interactions of α-thalassemia.

Prenatal diagnostic errors in hemoglobin Bart's hydrops fetalis caused by rare genetic interactions of α-thalassemia.

Journal: Diagnosis (Berlin, Germany)

Published: July 02, 2024

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

Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program.

Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program.

Journal: PloS one

Published: October 31, 2022

Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression.

Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression.

Journal: International journal of laboratory hematology

Published: October 01, 2022

α0-thalassemia in affected fetuses with hemoglobin E-β0-thalassemia disease in a high-risk population in Thailand.

α0-thalassemia in affected fetuses with hemoglobin E-β0-thalassemia disease in a high-risk population in Thailand.

Journal: American journal of translational research

Published: November 12, 2021

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.

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.

Journal: Orphanet journal of rare diseases

Published: October 12, 2021

Generation of a single-tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies.

Generation of a single-tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies.

Journal: International journal of laboratory hematology

Published: August 17, 2021

Genetic and non-genetic factors affecting hemoglobin A2 expression in a large cohort of Thai individuals: implication for population screening for thalassemia.

Genetic and non-genetic factors affecting hemoglobin A2 expression in a large cohort of Thai individuals: implication for population screening for thalassemia.

Journal: American journal of translational research

Published: April 29, 2021

Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-β 0-Thalassemia Diseases.

Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-β 0-Thalassemia Diseases.

Journal: Laboratory medicine

Published: February 02, 2021

Showing 1-12 of 53

Last Updated: 09/26/2026