Minoru Horie

26PUBLICATIONS
230CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Respiratory diseasesPredictive and prognostic markersNeurology and neuromuscular diseasesNeurogenetics
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Publications (26)

|May 11, 2026
Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel disease.

|Jan 26, 2026
Phenotypic Severity of SCN5A-Related Bradycardia Is Independent of Dominant-Negative and Coupled Gating Effects.

Ayami Tano, Koichi Kato, Kohei Yamauchi

|Dec 19, 2025
Catecholaminergic polymorphic ventricular tachycardia mediated by ryanodine receptor 2: a validated risk stratification.

Krystien V Lieve, Christian van der Werf, Dania Kallas

|Nov 04, 2025
Functional and pharmacological investigation of novel and de novo KCND3 variants identified in patients with neurodevelopmental disorders.

Byambajav Tserenlkham, Koichiro Takayama, Dimitar P Zankov

|Feb 11, 2025
SCN5A variant type-dependent risk prediction in Brugada syndrome.

Takanori Aizawa, Takeru Makiyama, Hai Huang

|Sep 24, 2024
Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve KCNH2-LQTS Variant Classification and Cardiac Event Risk Stratification.

Matthew J O'Neill, Chai-Ann Ng, Takanori Aizawa

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Frequent Collaborators

20 joint publications

Seiko Ohno

9 joint publications

Koichi Kato

7 joint publications

Vincent Probst

6 joint publications

Naomasa Makita