Supan Fuchareon (Supan Fucharoen, S Fucharoen)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 24

Top Venues

International journal of laboratory hematology

PloS one

Medical science monitor basic research

Journal of clinical pathology

Khon Kaen University

Kyushu University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Khon Kaen University

Thailand

Director :: Centre for Research and Development of Medical Diagnostic Laboratories

Education History

Kyushu University Oct 01 1986 - Sep 30 1990

Japan

PHD :: Research Laboratory for Genetic Information

Publications

Kritsada Singha, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fuchareon
Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program. PloS one 18 (4) (2023)
Areeda Arong, Hathichanok Srivorakun, Attawut Chaibunruang, Supan Fuchareon, Goonnapa Fucharoen, Sengchanh Kounnavong, Kanokwan Sanchaisuriya
Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression. International journal of laboratory hematology (2023)
Thinzar Win Pyae, Kanokwan Sanchaisuriya, Surasak Athikamanon, Pattara Sanchaisuriya, Hataichanok Srivorakun, Attawut Chaibunruang, Supan Fuchareon
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. PloS one 18 (6) (2023)
Kritsada Singha, Nattiya Teawtrakul, Goonnapa Fucharoen, Supan Fuchareon
Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series. Journal of clinical pathology (2023)
Nang Ei Ei Aung, Supawadee Yamsri, Nattiya Teawtrakul, Piyawan Kamsaen, Supan Fuchareon
FLT3 Gene Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand. Medical science monitor basic research 28 (2022)
Rossarin Karnpean, Nawinda Vanichakulthada, Wanwisa Suwannaloet, Ruttiya Thongrung, Sanita Singsanan, Nattapol Prakobkaew, Goonnapa Fucharoen, Supan Fuchareon
Anemia, iron deficiency, and thalassemia among the Thai population inhabiting at the Thailand-Lao PDR-Cambodia triangle. Scientific reports 12 (1) (2022)
Nang Ei Ei Aung, Supawadee Yamsri, Nattiya Teawtrakul, Piyawan Kamsaen, Supan Fuchareon
FLT3 Gene Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand. Medical science monitor basic research 28 (2022)
Sanita Singsanan, Supawadee Yamsri, Kanjana Pangjit, Phairo Saenwang, Rossarin Karnpean, Supan Fuchareon
Five Variable Number of Tandem Repeats Loci (D17S5, APOB, TPO Intron 10, IL-1α Intron 6, and CIAS1) in Thais and Application in the Prenatal Diagnostic Laboratory. Genetic testing and molecular biomarkers 26 (6) (2022)
Wittaya Jomoui, Hataichanok Srivorakun, Siriyakorn Chansai, Supan Fuchareon
Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis. PloS one 17 (4) (2022)
Kritsada Singha, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fuchareon
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. Orphanet journal of rare diseases 17 (1) (2022)
Nang Ei Ei Aung, Supawadee Yamsri, Nattiya Teawtrakul, Piyawan Kamsaen, Supan Fuchareon
FLT3 Gene Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand. Medical science monitor basic research 28 (2022)
Chayada Soontornpanawet, Kritsada Singha, Supan Fuchareon
Genotype and phenotype characteristics of homozygous and compound heterozygous β-thalassemia with 3.4 kb deletion. International journal of laboratory hematology 44 (5) (2022)
Phongsathorn Wichian, Supawadee Yamsri, Attawut Chaibunruang, Cholthicha KerdKaew, Dhanawan Thongsee, Hataichanok Srivorakun, Supan Fuchareon
Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis. Scandinavian journal of clinical and laboratory investigation 81 (7) (2021)
Kritsada Singha, Goonnapa Fucharoen, Supan Fuchareon
δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia. Annals of hematology 100 (8) (2021)
Anupong Pansuwan, Supawadee Yamsri, Duangrudee Changtrakul, Goonnapa Fucharoen, Supan Fuchareon
Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand. International journal of laboratory hematology 43 (4) (2021)
Benchawan Kingchaiyaphum, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Attawut Chaibunruang, Sonja Y Hess, Guy-Marino Hinnouho, Maxwell A Barffour, Kimbery R Wessells, Sengchanh Kounnavong, Supan Fuchareon
Hemoglobins F, A2 , and E levels in Laotian children aged 6-23 months with Hb E disorders: Effect of age, sex, and thalassemia types. International journal of laboratory hematology 42 (3) (2020)
Kritsada Singha, Surapon Wiangnon, Goonnapa Fucharoen, Arunee Jetsrisuparb, Patcharee Komwilaisak, Supan Fuchareon
Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart's disease: A hematological, molecular, and diagnostic aspects. International journal of laboratory hematology 42 (4) (2020)
Kritsada Singha, Attawut Chaibunruang, Bounpalisone Souvanlasy, Hataichanok Srivorakun, Supawadee Yamsri, Goonnapa Fucharoen, Supan Fuchareon
β-Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program. International journal of laboratory hematology 43 (3) (2020)
Roongnalin Bunthupanich, Rossarin Karnpean, Anuwat Pinyachat, Nawinda Jiambunsri, Nattapol Prakobkaew, Naruwat Pakdee, Supan Fuchareon, Suthat Fucharoen
Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand. Hemoglobin 44 (3) (2020)
Kritsada Singha, Hataichanok Srivorakun, Goonnapa Fucharoen, Supan Fuchareon
Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic. International journal of laboratory hematology 42 (1) (2019)
Kritsada Singha, Wachiraporn Taweenan, Goonnapa Fucharoen, Supan Fuchareon
Erythrocyte indices in a large cohort of β-thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia. International journal of laboratory hematology 41 (4) (2019)
Kritsada Singha, Rossarin Karnpean, Goonnapa Fucharoen, Supan Fuchareon
Dominant β-thalassaemia with unusually high Hb A2 and Hb F caused by βCD121(-G) (HBB:c.364delG) in exon 3 of β-globin gene. Journal of clinical pathology 73 (8) (2019)
Areeda Arong, Greetapop Wangwok, Kritsada Singha, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fuchareon
Differentiation of homozygous hemoglobin E and hemoglobin E-β0 -thalassemia in children. International journal of laboratory hematology 41 (3) (2018)
K Singha, H Srivorakun, G Fucharoen, Supan Fuchareon
Co-inheritance of α0 -thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications. International journal of laboratory hematology 39 (5) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Supan Fuchareon (Supan Fucharoen, S Fucharoen)