Minoru Horie

Professor

Shiga University of Medical Science

Japan

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Minoru Horie is a Professor at Shiga University of Medical Science in Japan. His research focuses on genetic cardiac disorders, particularly catecholaminergic polymorphic ventricular tachycardia, Brugada syndrome, and long QT syndrome. His recent publications highlight significant advancements in the clinical understanding and management of these conditions, as well as their genetic underpinnings.

Minoru Horie

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Articles (20)

Clinical Management of Brugada Syndrome: Commentary From the Experts

Application and validation of phenotype-enhanced variant classification in East Asian patients with catecholaminergic polymorphic ventricular tachycardia

Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

Disrupted Ca<sub>V</sub>1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model

<i>Retracted:</i> Computerized misinterpretation of <scp>QT</scp> interval in 12‐lead electrocardiogram and its clinical consequences: A case of recurrent syncope

A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients

Calmodulinopathy in Japanese Children ― Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy

Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathies.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (vol 77, pg 1534, 2013)

An NGS-based genotyping in LQTS; minor genes are no longer minor

Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1

Cardiac Emerinopathy A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction

Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense Mutation

Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese Population

Elevated Fasting Blood Glucose Levels Are Associated With Lower Cognitive Function, With a Threshold in Non-Diabetic Individuals: A Population-Based Study

Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan (vol 77, pg 1705, 2013)

Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Collaborators (16)

Hiroyuki MISHIMA

Hiroshi Tada

carla spazzolini

Elijah R Behr

Kazuhisa Chonabayashi

Federica Dagradi

Christian van der Werf

Michael Toft Overgaard

Joe-Elie Salem

Mette Nyegaard

Luca Sala

Henrik Kjærulf Jensen

Lee Eckhardt

Mathis Korseberg Stokke

Maarten P van den Berg

julien barc

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