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Proceedings of the National Academy of Sciences of the United States of America|September 2, 2008
Transcriptome-based systematic identification of extracellular matrix proteinsRi-ichiroh Manabe, Ko Tsutsui, Tomiko Yamada, et al.
Clinical Cardiology|November 22, 2022
A multicenter prospective randomized study comparing the incidence of periprocedural cerebral embolisms caused by catheter ablation of atrial fibrillation between cryoballoon and radiofrequency ablation (Embo-Abl study): Study designKoji Miyamoto, Koshiro Kanaoka, Yasutoshi Ohta, et al.
Structure (London, England : 1993)|December 12, 2017
Crystal Structures of Human Orexin 2 Receptor Bound to the Subtype-Selective Antagonist EMPARyoji Suno, Kanako Terakado Kimura, Takanori Nakane, 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.
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|January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic ConditionJason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.
Circulation|May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeNajim Lahrouchi, Rafik Tadros, Lia Crotti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
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