Keiko Sonoda
Suita, Japan
Last Updated: 09/26/2026
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Found 27 publications
A Genome-Wide Association Study Reveals Desmoglein-2 Predominance in Japanese Arrhythmogenic Cardiomyopathy.
Journal: Journal of arrhythmia
Published: October 22, 2025
Long-Term Arrhythmic Outcomes of KCNJ2 Variant Carriers in Japan.
Journal: Circulation. Genomic and precision medicine
Published: September 30, 2025
Functional and pharmacological investigation of novel and de novo KCND3 variants identified in patients with neurodevelopmental disorders.
Journal: Journal of human genetics
Published: September 17, 2025
Biventricular Dysfunction in Knock-in Mice With Dsg2 Variants Specific for Japanese Arrhythmogenic Right Ventricular Cardiomyopathy.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: August 31, 2025
Clinical Impact of Genetic Testing for Long QT Syndrome - Evidence From a Nationwide LQTS Registry in Japan.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: March 30, 2025
SCN5A variant type-dependent risk prediction in Brugada syndrome.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: November 14, 2024
Sex-specific clinical course of young patients with Brugada syndrome.
Journal: European heart journal
Published: August 31, 2024
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome.
Journal: JACC. Clinical electrophysiology
Published: September 29, 2021
Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1.
Journal: Heart (British Cardiac Society)
Published: August 23, 2021
Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias.
Journal: Circulation. Genomic and precision medicine
Published: August 13, 2021
LMNA Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated Cardiomyopathy.
Journal: Circulation. Genomic and precision medicine
Published: August 21, 2020
Last Updated: 09/26/2026