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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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Contributor content

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

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

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

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

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

Genome-wide methylation profiles in coronary artery ectasia

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

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