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Professor Jyh-Ming Juang

National Taiwan University Hospital, Taipei (Taiwan)

Member of:

European Society of Cardiology

Dr. Juang is currently an associate professor, Department of Internal Medicine, College of Medicine, National Taiwan University and an attending physician of Cardiology, Division of Cardiology, Department of Internal Medicine, National Taiwan University Hospital in Taiwan. He earned the Fellowship of Cardiology at Barnes-Jewish Hospital of Washington University in St. Louis in USA, and Master’s Degree of genetic medicine at Washington University in St. Louis School of Medicine in 2009. He received Ph. at the Institute of Physiology at the College of Medicine, National Taiwan University. In addition, he was ever awarded a Young Investigator Award (the Best Oral Presentation)/ 5th Asian Pacific Society of Hypertension in 2006 and a Best Poster in ESC 2017. His research focuses on the genetics of inheritable cardiac diseases including Long QT syndrome, Brugada syndrome, CPVT, Early Repolarization Syndrome, Idiopathic VF and HCM etc. He published >120 SCI papers in international journals.

Identification of genetic variants by using a whole exome sequencing approach in Taiwanese patients with Brugada Syndrome

Event: ESC Congress 2024

Topic: Ion Channel Disorders

Session: Sudden cardiac death: insight

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The impact of sarcomeric mutations on myocardial fibrosis and ventricular diastolic function in hypertrophic cardiomyopathy (SADS-TW HCM registry study)

Event: ESC Congress 2019

Topic: Systolic and Diastolic Function

Session: Cardiovascular magnetic resonance in myocarditis/HCM

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Validating previously reported brugada syndrome-associated common variants identified in caucasian population in the han chinese brs cohort in taiwan: SADS-BrS registry

Event: ESC Congress 2019

Topic: Arrhythmias

Session: Electrophysiology and arrhythmias

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Entropy-based algorithm for atrial fibrillation detection using photoplethysomgraphic signal recorded by a smart watch

Event: ESC Congress 2019

Topic: Noninvasive Diagnostic Methods

Session: Arrhythmias

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Functional studies of a novel copy number deletion in GSTM3 gene associated with increase of ventricular arrhythmia in patients with Brugada syndrome and ICD implantation

Event: ESC Congress 2018

Topic: Ion Channels, Electrophysiology

Session: Ion channels - Related pathologies

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Genome-wide methylation profiles in coronary artery ectasia

Event: ESC Congress 2017

Topic: Inflammation, growth factors and signal transduction-vascular

Session: Inflammation and grown factors

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Trans-ethnic fine mapping of previously identified QT interval loci in han chinese discover ethnic-specific signals associated with inflammation pathway

Event: ESC Congress 2017

Topic: Genetics and gene therapy

Session: Best Posters in genetics and gene therapy

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