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Junichi Ozawa
Observed names:
J Ozawa,
J. Ozawa,
OZAWA, Junichi
Institution:
Nagaoka Red Cross Hospital
Observed institutions:
Shiga University of Medical Science,
Shiga University,
Niigata City General Hospital,
Nagaoka Red Cross Hospital,
Niigata University Medical and Dental Hospital,
Niigata University
show all 6
ORCID:
0000-0002-9177-6458
Observed ORCID:
0000-0002-9177-6458
OpenAlex ID:
A5042134014
SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups
2018
·
Alban-Elouen Baruteau
, Florence Kyndt
, et al.
·
European Heart Journal
·
49
PDF
Copy number variations of SCN5A in Brugada syndrome
2018
·
Keiko Sonoda
, Seiko Ohno
, et al.
·
Heart Rhythm
·
35
Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1 ― Modified Schwartz Score ―
2018
·
Junichi Ozawa
, Seiko Ohno
, et al.
·
Circulation Journal
·
29
PDF
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes
2016
·
Mari Ichikawa
, Takeshi Aiba
, et al.
·
Circulation Journal
·
26
PDF
A novel CACNA1C mutation identified in a patient with Timothy syndrome without syndactyly exerts both marked loss- and gain-of-function effects
2018
·
Junichi Ozawa
, Seiko Ohno
, et al.
·
HeartRhythm Case Reports
·
20
PDF
Efficacy of SubcutAneous implantable cardioVErter-defibrillators in ≤18 year-old CHILDREN: SAVE-CHILDREN registry
2022
·
Hitoshi Mori
, Naokata Sumitomo
, et al.
·
International Journal of Cardiology
·
18
Novel electrocardiographic criteria for short QT syndrome in children and adolescents
2021
·
Hiroshi Suzuki
, Minoru Horie
, et al.
·
EP Europace
·
18
Short QT syndrome in a boy diagnosed on screening for heart disease
2014
·
Hiroshi Suzuki
, Satoshi Hoshina
, et al.
·
Pediatrics International
·
16
PDF
Pediatric Cohort With Long QT Syndrome – KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms –
2016
·
Junichi Ozawa
, Seiko Ohno
, et al.
·
Circulation Journal
·
15
PDF
An NGS-based genotyping in LQTS; minor genes are no longer minor
2020
·
Seiko Ohno
, Junichi Ozawa
, et al.
·
Journal of Human Genetics
·
14
School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome
2021
·
Megumi Fukuyama
, Minoru Horie
, et al.
·
EP Europace
·
12
High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8
2020
·
Megumi Fukuyama
, Seiko Ohno
, et al.
·
Circulation Journal
·
11
PDF
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano–Ward syndrome under double mutations and acquired long QT syndrome under heterozygote
2016
·
Yusuke Fujii
, Yuichi Matsumoto
, et al.
·
Journal of Cardiology
·
11
Two Cases of New Coronary Aneurysms That Developed in the Late Period After Kawasaki Disease
2012
·
Junichi Ozawa
, Hiroshi Suzuki
, et al.
·
Pediatric Cardiology
·
10
Dynamic QT Changes in Long QT Syndrome Type 8
2018
·
Mizuki Harada
, Hiroshi Suzuki
, et al.
·
Circulation Journal
·
8
PDF
A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant
2024
·
Hiromi Nyuzuki
, Junichi Ozawa
, et al.
·
Human Genome Variation
·
5
Congenital Short QT Syndrome ― Review Focused on KCNQ1 p.Val141Met Variant ―
2025
·
Minoru Horie
, Hirofumi Saiki
, et al.
·
Circulation Journal
·
4
PDF
Preterm Infant with Generalized Arterial Calcification of Infancy Who Survived Due to Early Diagnosis and Appropriate Treatment with Bisphosphonates: A Case Report
2024
·
Masato Tanaka
, Akira Kobayashi
, et al.
·
Children
·
4
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome
2022
·
Keisuke Suzuki
, Keiko Sonoda
, et al.
·
JACC. Clinical electrophysiology
·
4
Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants
2024
·
Asami Kashiwa
, Hideki Itoh
, et al.
·
Heart Rhythm
·
3
Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
2022
·
Junichi Ozawa
, Seiko Ohno
, et al.
·
Scientific Reports
·
3
PDF
Beckwith-Wiedemann syndrome with long QT caused by a deletion involving KCNQ1 but not KCNQ1OT1:TSS-DMR
2022
·
Tatsuki Urakawa
, Junichi Ozawa
, et al.
·
European Journal of Medical Genetics
·
2
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family
2016
·
Mari Ichikawa
, Seiko Ohno
, et al.
·
Internal Medicine
·
2
PDF
QT延長症候群8型患者において高頻度なlate-appearing T波
2020
·
Megumi Fukuyama
, Seiko Ohno
, et al.
·
Circulation
·
1
SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups
2019
·
Alban-Elouen Baruteau
, Florence Kyndt
, et al.
·
Archives of Cardiovascular Diseases Supplements
·
1
PDF
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Works count:
38
Citation count:
322
H-index:
11
I10-index:
14
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