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Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Heart Rhythm. 2020 Dec;17(12):2145-2153. doi: 10.1016/j.hrthm.2020.06.027. Epub 2020 Jun 30.
Heart Rhythm. 2020.
PMID: 32619740
Clinical Characteristics of SCN5A p.R965C Carriers: A Common Founder Variant Predisposing to Brugada Syndrome in Thailand.
Chimparlee N, Prechawat S, Khongphatthanayothin A, Mauleekoonphairoj J, Lekchuensakul S, Wongcharoen W, Makarawate P, Sahasatas D, Krittayaphong R, Amnueypol M, Anannab A, Ngarmukos T, Vardhanabhuti S, Sutjaporn B, Wandee P, Veerakul G, Bezzina CR, Poovorawan Y, Nademanee K.
Chimparlee N, et al. Among authors: sutjaporn b.
Circ Genom Precis Med. 2021 Jun;14(3):e003229. doi: 10.1161/CIRCGEN.120.003229. Epub 2021 Jun 7.
Circ Genom Precis Med. 2021.
PMID: 34092119
Clinical Trial.
No abstract available.
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Phenotype prediction and characterization of 25 pharmacogenes in Thais from whole genome sequencing for clinical implementation.
Mauleekoonphairoj J, Chamnanphon M, Khongphatthanayothin A, Sutjaporn B, Wandee P, Poovorawan Y, Nademanee K, Pongpanich M, Chariyavilaskul P.
Mauleekoonphairoj J, et al. Among authors: sutjaporn b.
Sci Rep. 2020 Nov 3;10(1):18969. doi: 10.1038/s41598-020-76085-3.
Sci Rep. 2020.
PMID: 33144648
Free PMC article.
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A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population.
Mauleekoonphairoj J, Tongsima S, Khongphatthanayothin A, Jurgens SJ, Zimmerman DS, Sutjaporn B, Wandee P, Bezzina CR, Nademanee K, Poovorawan Y.
Mauleekoonphairoj J, et al. Among authors: sutjaporn b.
Sci Rep. 2023 Jul 31;13(1):12360. doi: 10.1038/s41598-023-39429-3.
Sci Rep. 2023.
PMID: 37524845
Free PMC article.
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Metagenomic analysis of viral genes integrated in whole genome sequencing data of Thai patients with Brugada syndrome.
Chitcharoen S, Phokaew C, Mauleekoonphairoj J, Khongphatthanayothin A, Sutjaporn B, Wandee P, Poovorawan Y, Nademanee K, Payungporn S.
Chitcharoen S, et al. Among authors: sutjaporn b.
Genomics Inform. 2022 Dec;20(4):e44. doi: 10.5808/gi.22047. Epub 2022 Dec 30.
Genomics Inform. 2022.
PMID: 36617651
Free PMC article.
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