← Back to directory

Minoru Horie

Researcher Next ID · RN-036005

Researcher · Biochemistry, Genetics and Molecular Biology

Shiga University of Medical Science

Ōtsu, Japan

Accepting doctoral researchersFunding unknown
Works count
1,079
Citation count
28,260
H-index
83
i10-index
436

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Cardiac electrophysiology and arrhythmias
Ion channel regulation and function
Cardiac Arrhythmias and Treatments
Cardiac Imaging and Diagnostics
Atrial Fibrillation Management and Outcomes

Publications

  • Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

    European Heart Journal · 2019 · 10.1093/eurheartj/ehz311

  • Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome

    Circulation · 2017 · 10.1161/circulationaha.117.027983

  • J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

    Heart Rhythm · 2016 · https://doi.org/10.1016/j.hrthm.2016.05.024

  • Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

    Nature Communications · 2016 · 10.1038/ncomms11067

  • The genetics underlying acquired long QT syndrome: impact for genetic screening

    European Heart Journal · 2015 · 10.1093/eurheartj/ehv695

  • Ultrastructural Maturation of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes in a Long-Term Culture

    Circulation Journal · 2013 · 10.1253/circj.cj-12-0987

  • Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

    Nature Genetics · 2013 · https://doi.org/10.1038/ng.2712

  • HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

    Heart Rhythm · 2013 · https://doi.org/10.1016/j.hrthm.2013.05.014

  • Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

    EP Europace · 2013 · https://doi.org/10.1093/europace/eut272

  • Executive Summary: HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

    Heart Rhythm · 2013 · 10.1016/j.hrthm.2013.07.021

  • High prevalence of early repolarization in short QT syndrome

    Heart Rhythm · 2010 · https://doi.org/10.1016/j.hrthm.2010.01.012

  • Long-Term Prognosis of Probands With Brugada-Pattern ST-Elevation in Leads V 1 –V 3

    Circulation Arrhythmia and Electrophysiology · 2009 · 10.1161/circep.108.816892

  • The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

    Journal of Clinical Investigation · 2008 · 10.1172/jci34057

  • A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation

    Journal of the American College of Cardiology · 2008 · 10.1016/j.jacc.2008.07.013

  • Prevalence of atrial fibrillation in the general population of Japan: An analysis based on periodic health examination

    International Journal of Cardiology · 2008 · 10.1016/j.ijcard.2008.06.029

  • Relationship Between Renal Function and Plasma Brain Natriuretic Peptide in Patients With Heart Failure

    Journal of the American College of Cardiology · 2006 · 10.1016/j.jacc.2005.10.038

  • The Jervell and Lange-Nielsen Syndrome

    Circulation · 2006 · 10.1161/circulationaha.105.592899

  • Electrocardiographic Features in Andersen-Tawil Syndrome Patients With KCNJ2 Mutations

    Circulation · 2005 · 10.1161/circulationaha.104.472498

  • Immediate Administration of Mineralocorticoid Receptor Antagonist Spironolactone Prevents Post-Infarct Left Ventricular Remodeling Associated With Suppression of a Marker of Myocardial Collagen Synthesis in Patients With First Anterior Acute Myocardial Infarction

    Circulation · 2003 · 10.1161/01.cir.0000068340.96506.0f

  • Exercise Stress Test Amplifies Genotype-Phenotype Correlation in the LQT1 and LQT2 Forms of the Long-QT Syndrome

    Circulation · 2003 · https://doi.org/10.1161/01.cir.0000048142.85076.a2

  • Genomic structure and mutations in adipose-specific gene, adiponectin

    International Journal of Obesity · 2000 · 10.1038/sj.ijo.0801244

  • Cloning and Functional Characterization of a Novel ATP-sensitive Potassium Channel Ubiquitously Expressed in Rat Tissues, including Pancreatic Islets, Pituitary, Skeletal Muscle, and Heart

    Journal of Biological Chemistry · 1995 · https://doi.org/10.1074/jbc.270.11.5691

  • Long-term prognosis for patients with variant angina and influential factors.

    Circulation · 1988 · https://doi.org/10.1161/01.cir.78.1.1

  • Voltage‐dependent magnesium block of adenosine‐triphosphate‐sensitive potassium channel in guinea‐pig ventricular cells.

    The Journal of Physiology · 1987 · 10.1113/jphysiol.1987.sp016572

Current projects

    No projects listed.