Citations (44)
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Phongsathorn Wichian, Supawadee Yamsri, Attawut Chaibunruang, Cholthicha KerdKaew, Dhanawan Thongsee, Hataichanok Srivorakun & Supan Fucharoen. (2021) 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, pages 557-563.
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Roongnalin Bunthupanich, Rossarin Karnpean, Anuwat Pinyachat, Nawinda Jiambunsri, Nattapol Prakobkaew, Naruwat Pakdee, Supan Fucharoen & Suthat Fucharoen. (2020) Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand. Hemoglobin 44:3, pages 162-167.
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Aye Chan Pyae, Hataichanok Srivorakun, Attawut Chaibunruang, Kritsada Singha, Kanchana Tomanakarn, Goonnapa Fucharoen & Supan Fucharoen. (2019) Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia . Hemoglobin 43:4-5, pages 254-257.
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Tuan Mai Anh, Kanokwan Sanchaisuriya, Giang Nguyen Kieu, Dung Nguyen Tien, Huong Bui Thi Thu, Pattara Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen & Frank P. Schelp. (2019) Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam. Hemoglobin 43:4-5, pages 249-253.
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Wittaya Jomoui, Prapaporn Panichchob, Punchita Rujirachaivej, Sitthichai Panyasai & Wanicha Tepakhan. (2019) Coinheritance of Hb A2-Melbourne (HBD: c.130G>A) and Hb E (HBB: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A2-Melbourne and Hb A2-Lampang (HBD: c.142G>A) in a Single Tube. Hemoglobin 43:3, pages 214-217.
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Thongperm Munkongdee, Jatuporn Tanakulmas, Punnee Butthep, Pranee Winichagoon, Barbara Main, Miriam Yiannakis, Joby George, Robyn Devenish, Suthat Fucharoen & Saovaros Svasti. (2016) Molecular Epidemiology of Hemoglobinopathies in Cambodia. Hemoglobin 40:3, pages 163-167.
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Hoa Van Nguyen, Kanokwan Sanchaisuriya, Dung Nguyen, Hoa Thi Thuy Phan, Sirivara Siridamrongvattana, Pattara Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen & Frank P. Schelp. (2013) Thalassemia and Hemoglobinopathies in Thua Thien Hue Province, Central Vietnam. Hemoglobin 37:4, pages 333-342.
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Articles from other publishers (37)
Manit Nuinoon. 2023. Thalassemia Syndromes - New Insights and Transfusion Modalities. Thalassemia Syndromes - New Insights and Transfusion Modalities.
Kritsada Singha, Wanicha Tepakhan, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Anupong Pansuwan, Goonnapa Fucharoen & Supan Fucharoen. (2023) A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation. Clinica Chimica Acta 551, pages 117615.
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Sitthichai Panyasai, Surada Satthakarn & Amphai Phasit. (2023) Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis. Heliyon 9:8, pages e19116.
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Thinzar Win Pyae, Kanokwan Sanchaisuriya, Surasak Athikamanon, Pattara Sanchaisuriya, Hataichanok Srivorakun, Attawut Chaibunruang & Supan Fucharoen. (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. PLOS ONE 18:6, pages e0287527.
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Areeda Arong, Hathichanok Srivorakun, Attawut Chaibunruang, Supan Fucharoen, Goonnapa Fucharoen, Sengchanh Kounnavong & Kanokwan Sanchaisuriya. (2023)
Hemoglobin
EE
disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression
. International Journal of Laboratory Hematology 45:3, pages 387-393.
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Vilaysone Khounvisith, Sonephet Saysouligno, Bounpalisone Souvanlasy, Somxay Billamay, Sodaly Mongkhoune, Bounta Vongphachanh, Chantal J Snoeck, Antony P Black, Claude P Muller & Judith M Hübschen. (2023) Hepatitis B virus and other transfusion-transmissible infections in child blood recipients in Lao People’s Democratic Republic: a hospital-based study. Archives of Disease in Childhood 108:1, pages 15-19.
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Kritsada Singha, Supawadee Yamsri, Attawut Chaibunruang, Hataichanok Srivorakun, Kanokwan Sanchaisuriya, Goonnapa Fucharoen & Supan Fucharoen. (2022) 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.
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Rossarin Karnpean, Nawinda Vanichakulthada, Wanwisa Suwannaloet, Ruttiya Thongrung, Sanita Singsanan, Nattapol Prakobkaew, Goonnapa Fucharoen & Supan Fucharoen. (2022) Anemia, iron deficiency, and thalassemia among the Thai population inhabiting at the Thailand-Lao PDR-Cambodia triangle. Scientific Reports 12:1.
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Wittaya Jomoui, Hataichanok Srivorakun, Siriyakorn Chansai & Supan Fucharoen. (2022) 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, pages e0267832.
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Phongsathorn Wichian, Supawadee Yamsri, Kanokwan Sanchaisuriya & Supan Fucharoen. (2021) Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-β 0-Thalassemia Diseases. Laboratory Medicine 52:5, pages 460-468.
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Kritsada Singha, Attawut Chaibunruang, Bounpalisone Souvanlasy, Hataichanok Srivorakun, Supawadee Yamsri, Goonnapa Fucharoen & Supan Fucharoen. (2020) 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, pages 500-505.
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Wanicha Tepakhan & Wittaya Jomoui. (2021) Rapid Molecular Detection for Differentiation of Homozygous HbE and ß0-Thalassemia/HbE in Samples Related With HbE >80% and Variable HbF Levels. Laboratory Medicine 52:3, pages 232-239.
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Ibrahim Kalle Kwaifa, Mei I. Lai & Sabariah Md Noor. (2020) Non-deletional alpha thalassaemia: a review. Orphanet Journal of Rare Diseases 15:1.
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Lucky Poh Wah Goh, Eric Tzyy Jiann Chong & Ping-Chin Lee. (2020) Prevalence of Alpha(α)-Thalassemia in Southeast Asia (2010–2020): A Meta-Analysis Involving 83,674 Subjects. International Journal of Environmental Research and Public Health 17:20, pages 7354.
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Kasorn Tiewsiri, Somjate Manipalviratn, Warachaya Sutheesophon, Preeda Vanichsetakul, Piyarat Thaijaroen, Pagawadee Ketcharoon, Cara K. Bradley, Steven J. McArthur, Weena Krutsawad, James T. A. Marshall & Konstantinos I. Papadopoulos. (2020) The First Asian, Single-Center Experience of Blastocyst Preimplantation Genetic Diagnosis with HLA Matching in Thailand for the Prevention of Thalassemia and Subsequent Curative Hematopoietic Stem Cell Transplantation of Twelve Affected Siblings. BioMed Research International 2020, pages 1-10.
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Kritsada Singha, Hataichanok Srivorakun, Goonnapa Fucharoen & Supan Fucharoen. (2019) Molecular basis of Hb H and AEBart’s diseases in the Lao People’s Democratic Republic. International Journal of Laboratory Hematology 42:1, pages 23-27.
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Sayphonh Phanmany, Supantitra Chanprasert, Thongperm Munkongdee, Saovaros Svasti & Kamonlak Leecharoenkiat. (2019) Molecular prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People’s Democratic Republic. International Journal of Laboratory Hematology 41:5, pages 650-656.
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Kanittha Mankhemthong, Arunee Phusua, Sudjai Suanta, Pitipong Srisittipoj, Pimlak Charoenkwan & Torpong Sanguansermsri. (2019) Molecular characteristics of thalassemia and hemoglobin variants in prenatal diagnosis program in northern Thailand. International Journal of Hematology 110:4, pages 474-481.
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Thanyaornwanya Charoenwijitkul, Kritsada Singha, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Phuthita Thepphitak, Preawwalee Wintachai, Rossarin Karnpean & Supan Fucharoen. (2019) Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics. Clinical Biochemistry 71, pages 31-37.
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Maxwell A. Barffour, Guy-Marino Hinnouho, Sengchanh Kounnavong, K. Ryan Wessells, Kethmany Ratsavong, Bangone Bounheuang, Bigphone Chanhthavong, Dalaphone Sitthideth, Khanpaseuth Sengnam, Charles D. Arnold, Kenneth H. Brown & Sonja Y. Hess. (2019) Effects of Daily Zinc, Daily Multiple Micronutrient Powder, or Therapeutic Zinc Supplementation for Diarrhea Prevention on Physical Growth, Anemia, and Micronutrient Status in Rural Laotian Children: A Randomized Controlled Trial. The Journal of Pediatrics 207, pages 80-89.e2.
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Wittaya Jomoui, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Patnaree Charoenwijitkul, Jitpanu Maneesarn, Xiangmin Xu & Supan Fucharoen. (2017) Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart’s hydrops fetalis syndrome. Journal of Human Genetics 62:8, pages 747-754.
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Nga Thi Nguyen, Kanokwan Sanchaisuriya, Pattara Sanchaisuriya, Hoa Van Nguyen, Hoa Thi Thuy Phan, Goonnapa Fucharoen & Supan Fucharoen. (2017) Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups. Journal of Community Genetics 8:3, pages 221-228.
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Wittaya Jomoui, Goonnapa Fucharoen, Kanokwan Sanchaisuriya & Supan Fucharoen. (2017)
Screening of (–
SEA
) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies
. Journal of Clinical Pathology 70:1, pages 63-68.
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Wanicha Tepakhan, Supawadee Yamsri, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Xiangmin Xu & Supan Fucharoen. (2016) Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder. Blood Cells, Molecules, and Diseases 59, pages 85-91.
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Wittaya Jomoui, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Van Hoa Nguyen & Supan Fucharoen. (2015) Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis. PLOS ONE 10:12, pages e0145230.
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Wanicha Tepakhan, Supawadee Yamsri, Goonnapa Fucharoen, Kanokwan Sanchaisuriya & Supan Fucharoen. (2015) Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome. Annals of Hematology 94:7, pages 1093-1098.
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Jiraporn Kuesap, W. Chaijaroenkul, K. Rungsihirunrat, K. Pongjantharasatien & Kesara Na-Bangchang. (2015) Coexistence of Malaria and Thalassemia in Malaria Endemic Areas of Thailand. The Korean Journal of Parasitology 53:3, pages 265-270.
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Jie Zhang, Jing He, Xiao-Hong Zeng, Shi-Jun Ge, Yu Huang, Jie Su, Xue-Mei Ding, Ji-Qing Yang, Yong-Jiu Cao, Hong Chen, Ying-Hong Zhang & Bao-Sheng Zhu. (2015) Genetic Heterogeneity of the β-Globin Gene in Various Geographic Populations of Yunnan in Southwestern China. PLOS ONE 10:4, pages e0122956.
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Supawadee Yamsri, Kritsada Singha, Thanet Prajantasen, Wachiraporn Taweenan, Goonnapa Fucharoen, Kanokwan Sanchaisuriya & Supan Fucharoen. (2015) A large cohort of β+-thalassemia in Thailand: Molecular, hematological and diagnostic considerations. Blood Cells, Molecules, and Diseases 54:2, pages 164-169.
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Danny Koh Xuan Rong, Endom Ismail, Raja Zahratul Azma Raja Sabudin, Noor Hamidah Hussin & Ainoon Othman. Hemoglobinopathies and thalassemia screening among Senoi Orang Asli in Peninsular Malaysia. Hemoglobinopathies and thalassemia screening among Senoi Orang Asli in Peninsular Malaysia.
Somphou Sayasone, Jürg Utzinger, Kongsap Akkhavong & Peter Odermatt. (2015) Multiparasitism and intensity of helminth infections in relation to symptoms and nutritional status among children: A cross-sectional study in southern Lao People's Democratic Republic. Acta Tropica 141, pages 322-331.
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Hataichanok Srivorakun, Kritsada Singha, Goonnapa Fucharoen, Kanokwan Sanchaisuriya & Supan Fucharoen. (2014) A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration. PLoS ONE 9:9, pages e108365.
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Patcharawadee Prayalaw, Goonnapa Fucharoen & Supan Fucharoen. (2014) Routine screening for α-thalassaemia using an immunochromatographic strip assay for haemoglobin Bart's. Journal of Medical Screening 21:3, pages 120-125.
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Van Hoa Nguyen, Kanokwan Sanchaisuriya, Kasama Wongprachum, Mau Duyen Nguyen, Thi Thuy Hoa Phan, Van Thang Vo, Pattara Sanchaisuriya, Supan Fucharoen & Frank P. Schelp. (2014) Hemoglobin Constant Spring is markedly high in women of an ethnic minority group in Vietnam: A community-based survey and hematologic features. Blood Cells, Molecules, and Diseases 52:4, pages 161-165.
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Attawut Chaibunruang, Rossarin Karnpean, Goonnapa Fucharoen & Supan Fucharoen. (2014) Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand. Blood Cells, Molecules, and Diseases 52:4, pages 176-180.
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Attawut Chaibunruang, Simaporn Prommetta, Supawadee Yamsri, Goonnapa Fucharoen, Nattaya Sae-ung, Kanokwan Sanchaisuriya & Supan Fucharoen. (2013) Molecular and hematological studies in a large cohort of α0-thalassemia in northeast Thailand: Data from a single referral center. Blood Cells, Molecules, and Diseases 51:2, pages 89-93.
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Sirivara Siridamrongvattana, Nguyen Van Hoa, Kanokwan Sanchaisuriya, Nguyen Dung, Phan Thi Thuy Hoa, Pattara Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen & Frank P. Schelp. (2013) Burden of Anemia in Relation to Thalassemia and Iron Deficiency among Vietnamese Pregnant Women. Acta Haematologica 130:4, pages 281-287.
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