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Scientific Reports|July 31, 2023
A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented populationJohn Mauleekoonphairoj, Sissades Tongsima, Apichai Khongphatthanayothin, et al.
PNAS Nexus|December 19, 2025
Mutation-specific roles of sustained sodium current (INa) in guiding precision medicine for long QT syndrome type 3Vichaya Auvichayapat, Sarin Lekchuensakul, Pharawee Wandee, et al.
Heart Rhythm|April 28, 2025
Brugada Syndrome Ablation for the Prevention of Ventricular Fibrillation Episodes (BRAVE)Koonlawee Nademanee, Wanwarang Wongcharoen, Nitinan Chimparlee, et al.
Heart Rhythm|July 4, 2020
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in ThailandPattarapong Makarawate, Charlotte Glinge, Apichai Khongphatthanayothin, et al.
European Heart Journal|May 15, 2024
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk lociTaisuke Ishikawa, Tatsuo Masuda, Tsuyoshi Hachiya, et al.
Circulation|October 11, 2024
A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in ThailandRoddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli, et al.
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