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

Journal of human genetics, 2020-12, Vol.65 (12), p.1083-1091

2020

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Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome

Circulation Journal, 2024/06/25, Vol.88(7), pp.1176-1184

2024

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Impact of statin therapy on late target lesion revascularization after everolimus-eluting stent implantation according to pre-interventional vessel remodeling and vessel size of treated lesion

Heart and vessels, 2022-11, Vol.37 (11), p.1817-1828

2022

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

Circulation Journal, 2020/08/25, Vol.84(9), pp.1575-1581

2020

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Clopidogrel Use in CYP2C19 Loss-of-Function Carriers With High Bleeding Risk After Percutaneous Coronary Intervention

Circulation Journal, 2023/05/25, Vol.87(6), pp.755-763

2023

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High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8

Circulation Journal, 2020/03/25, Vol.84(4), pp.559-568

2020

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Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1

Heart (British Cardiac Society), 2022-06, Vol.108 (11), p.840-847

2022

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Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome

Europace (London, England), 2022-03, Vol.24 (3), p.497-510

2022

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Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly

Scientific reports, 2022-11, Vol.12 (1), p.18984-18984, Article 18984

2022

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School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome

Europace (London, England), 2022-10, Vol.24 (9), p.1496-1503

2022

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

Circulation Journal, 2023/11/24, Vol.87(12), pp.1828-1835

2023

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Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Circulation Journal, 2020/10/23, Vol.84(11), pp.2123

2020

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Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

Europace (London, England), 2014-12, Vol.16 (12), p.1828-1837

2014

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Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes

Circulation Journal, 2016/11/25, Vol.80(12), pp.2435-2442

2016

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Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Circulation Journal, 2013, Vol.77(6), pp.1534-1542

2013

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L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias

Circulation Journal, 2013, Vol.77(7), pp.1799-1806

2013

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A Common Mutation of Long QT Syndrome Type 1 in Japan

Circulation Journal, 2015/08/25, Vol.79(9), pp.2026-2030

2015

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Nonsense-mediated mRNA decay due to a CACNA1C splicing mutation in a patient with Brugada syndrome

Heart rhythm, 2014-04, Vol.11 (4), p.629-634

2014

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Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family

Internal Medicine, 2016, Vol.55(3), pp.259-262

2016

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Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome

Journal of cardiology, 2018-04, Vol.71 (4), p.401-408

2018

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Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome

Circulation Journal, 2023/12/01, pp.CJ-23-0409

2023

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Genetic screening of KCNJ8 in Japanese patients with J-wave syndromes or idiopathic ventricular fibrillation

Journal of arrhythmia, 2013-10, Vol.29 (5), p.261-264

2013

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

Heart rhythm, 2024-07, Vol.21 (7), p.1113-1120

2024

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Novel SCN10A variants associated with Brugada syndrome

Europace (London, England), 2016-06, Vol.18 (6), p.905-911

2016

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Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

Europace (London, England), 2014-12, Vol.16 (12), p.1828-1837

2014

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

Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome

Impact of statin therapy on late target lesion revascularization after everolimus-eluting stent implantation according to pre-interventional vessel remodeling and vessel size of treated lesion

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

Clopidogrel Use in CYP2C19 Loss-of-Function Carriers With High Bleeding Risk After Percutaneous Coronary Intervention

High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8

Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1

Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome

Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly

School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome

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

Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes

Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias

A Common Mutation of Long QT Syndrome Type 1 in Japan

Nonsense-mediated mRNA decay due to a CACNA1C splicing mutation in a patient with Brugada syndrome

Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family

Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome

Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome

Genetic screening of KCNJ8 in Japanese patients with J-wave syndromes or idiopathic ventricular fibrillation

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

Novel SCN10A variants associated with Brugada syndrome

Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

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