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Yuka Mizusawa

Jichi Medical University Saitama Medical Center · JP
Area of research
Cardiology and Cardiovascular Medicine · Molecular Biology
Research interest
Research interests include Cardiac electrophysiology and arrhythmias, Ion channel regulation and function, Cardiac Arrhythmias and Treatments, and ECG Monitoring and Analysis.
h-index
27
citations
3,103
works
91
NIH funding
primary concept
Medicine
email

Recent publications

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Nature Genetics 2022cited by 141position: middledoi
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
Circulation 2020cited by 140position: middledoi
<i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families
Circulation Genomic and Precision Medicine 2020cited by 64position: middledoi
Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome
Journal of the American College of Cardiology 2019cited by 70position: middledoi
Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome
Heart Rhythm 2019cited by 34position: middledoi
Fever-related arrhythmic events in the multicenter Survey on Arrhythmic Events in Brugada Syndrome
Heart Rhythm 2018cited by 88position: middledoi
Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients
Heart Rhythm 2018cited by 81position: middledoi
Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)
Heart Rhythm 2018cited by 76position: middledoi
Prognostic significance of fever-induced Brugada syndrome
Heart Rhythm 2016cited by 76position: firstdoi
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Nature Genetics 2013cited by 545position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Estelle Gandjbakhch · Université de Caen Normandie1 papers (2016–2016)Sami Viskin · Tel Aviv University1 papers (2016–2016)Aurélie Thollet · ERN GUARD-Heart1 papers (2016–2016)Frédéric Sacher · Hôpital Pellegrin1 papers (2016–2016)Dan Hu · Massachusetts Institute of Technology1 papers (2016–2016)Ahmad S. Amin · Amsterdam Neuroscience1 papers (2016–2016)Hanno L. Tan · Netherlands Heart Institute1 papers (2016–2016)Najim Lahrouchi · Massachusetts General Hospital1 papers (2016–2016)Philippe Maury · Technical University of Munich1 papers (2016–2016)Kui Hong · Nanchang University1 papers (2016–2016)Vincent Probst · Hôpital Nord1 papers (2016–2016)Arthur A.M. Wilde · Norton Healthcare1 papers (2016–2016)Arnon Adler · University Health Network1 papers (2016–2016)Charles Antzelevitch · Sidney Kimmel Cancer Center1 papers (2016–2016)Hiroshi Morita · Fujieda Municipal General Hospital1 papers (2016–2016)Dao Wen Wang · Tongji Hospital1 papers (2016–2016)Ofer Havakuk · Weizmann Institute of Science1 papers (2016–2016)