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Plos One|December 8, 2022
Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.Circulation. Genomic and Precision Medicine|September 16, 2020
Systematic Evaluation of <i>KCNQ1</i> Variant Using ACMG/AMP Guidelines and Risk Stratification in Long QT Syndrome Type 1Asami Kashiwa, Takeshi Aiba, Hisaki Makimoto, et al.Plos One|December 3, 2024
Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.Circulation. Cardiovascular Genetics|December 15, 2017
Gene-Based Risk Stratification for Cardiac Disorders in <i>LMNA</i> Mutation CarriersSuguru Nishiuchi, Takeru Makiyama, Takeshi Aiba, et al.Journal of the American Heart Association|September 15, 2016
Variants in the SCN5A Promoter Associated With Various Arrhythmia PhenotypesNobue Yagihara, Hiroshi Watanabe, Phil Barnett, et al.Heart (British Cardiac Society)|March 16, 2017
Arrhythmia risk and β-blocker therapy in pregnant women with long QT syndromeKohei Ishibashi, Takeshi Aiba, Chizuko Kamiya, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|March 30, 2025
Clinical Impact of Genetic Testing for Long QT Syndrome - Evidence From a Nationwide LQTS Registry in JapanTakeshi Aiba, Seiko Ohno, Misa Takegami, et al.Circulation. Cardiovascular Genetics|June 12, 2014
Novel calmodulin mutations associated with congenital arrhythmia susceptibilityNaomasa Makita, Nobue Yagihara, Lia Crotti, et al.Pageof 4