Shih-fan S. Yeh

Hsinchu, TNQ, Taiwan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

Genetic and clinical characteristics of catecholaminergic polymorphic ventricular tachycardia in a Taiwanese nationwide cohort.

Genetic and clinical characteristics of catecholaminergic polymorphic ventricular tachycardia in a Taiwanese nationwide cohort.

Journal: Journal of the Formosan Medical Association = Taiwan yi zhi

Published: December 09, 2023

Application and validation of phenotype-enhanced variant classification in East Asian patients with catecholaminergic polymorphic ventricular tachycardia.

Application and validation of phenotype-enhanced variant classification in East Asian patients with catecholaminergic polymorphic ventricular tachycardia.

Journal: Heart rhythm

Published: June 27, 2023

Develop and Apply Electrocardiography-Based Risk Score to Identify Community-Based Elderly Individuals at High-Risk of Mortality.

Develop and Apply Electrocardiography-Based Risk Score to Identify Community-Based Elderly Individuals at High-Risk of Mortality.

Journal: Frontiers in cardiovascular medicine

Published: July 08, 2021

Long-term outcomes and left ventricular diastolic function of sarcomere mutation-positive and mutation-negative patients with hypertrophic cardiomyopathy: a prospective cohort study.

Long-term outcomes and left ventricular diastolic function of sarcomere mutation-positive and mutation-negative patients with hypertrophic cardiomyopathy: a prospective cohort study.

Journal: European heart journal. Cardiovascular Imaging

Published: September 23, 2020

Role of electrocardiographic early repolarization pattern in long-term outcomes of a community-based middle-aged and geriatric ambulatory population: a prospective cohort study.

Role of electrocardiographic early repolarization pattern in long-term outcomes of a community-based middle-aged and geriatric ambulatory population: a prospective cohort study.

Journal: Aging

Published: August 08, 2020

GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death.

GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death.

Journal: EBioMedicine

Published: March 11, 2020

Metabolomic Analysis of Platelets of Patients With Aspirin Non-Response.

Metabolomic Analysis of Platelets of Patients With Aspirin Non-Response.

Journal: Frontiers in pharmacology

Published: November 13, 2018

Impact of Ancestral Differences and Reassessment of the Classification of Previously Reported Pathogenic Variants in Patients With Brugada Syndrome in the Genomic Era: A SADS-TW BrS Registry.

Impact of Ancestral Differences and Reassessment of the Classification of Previously Reported Pathogenic Variants in Patients With Brugada Syndrome in the Genomic Era: A SADS-TW BrS Registry.

Journal: Frontiers in genetics

Published: September 14, 2018

Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study.

Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study.

Journal: Annals of medicine

Published: July 08, 2017

Genome-wide methylation profiles in coronary artery ectasia.

Genome-wide methylation profiles in coronary artery ectasia.

Journal: Clinical science (London, England : 1979)

Published: October 29, 2016

Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome.

Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome.

Journal: Scientific reports

Published: August 07, 2014

Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.

Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.

Journal: Chinese medical journal

Published: April 26, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026