Qiuping Wu

No. 74, Zhongshan 2nd Road
Guangzhou, 510080, China

Last Updated: 09/26/2026

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Found 16 publications

Characterization of a novel SCN5A mutation associated with long QT syndrome and arrhythmogenic right ventricular cardiomyopathy in a family.

Characterization of a novel SCN5A mutation associated with long QT syndrome and arrhythmogenic right ventricular cardiomyopathy in a family.

Journal: Forensic science, medicine, and pathology

Published: July 10, 2024

Mutation in mitral valve prolapse susceptible gene DCHS1 causes familial mitral annular disjunction.

Mutation in mitral valve prolapse susceptible gene DCHS1 causes familial mitral annular disjunction.

Journal: Journal of medical genetics

Published: March 14, 2023

Targeted genetic analysis in a cohort of sporadic death from spontaneous rupture of thoracic aortic dissection in Han Chinese population.

Targeted genetic analysis in a cohort of sporadic death from spontaneous rupture of thoracic aortic dissection in Han Chinese population.

Journal: Forensic science international. Genetics

Published: March 12, 2023

The characteristics of thoracic aortic dissection in autopsy-diagnosed individuals: An autopsy study.

The characteristics of thoracic aortic dissection in autopsy-diagnosed individuals: An autopsy study.

Journal: Frontiers in cardiovascular medicine

Published: June 20, 2022

Xanthohumol inhibits tau protein aggregation and protects cells against tau aggregates.

Xanthohumol inhibits tau protein aggregation and protects cells against tau aggregates.

Journal: Food & function

Published: December 04, 2019

HCN4 Gene Variations in Sudden Unexplained Nocturnal Death Syndrome in the Southern Han Chinese Population.

HCN4 Gene Variations in Sudden Unexplained Nocturnal Death Syndrome in the Southern Han Chinese Population.

Journal: Journal of forensic sciences

Published: June 14, 2018

Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing.

Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing.

Journal: International journal of legal medicine

Published: January 14, 2018

Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.

Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.

Journal: Journal of the American Heart Association

Published: January 08, 2018

Course constructions: A case-base of forensic toxicology.

Course constructions: A case-base of forensic toxicology.

Journal: Journal of forensic and legal medicine

Published: December 25, 2016

The forensic pathological analysis of sport-related sudden cardiac death in Southern China.

The forensic pathological analysis of sport-related sudden cardiac death in Southern China.

Journal: Forensic sciences research

Published: November 26, 2016

Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go.

Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go.

Journal: Forensic sciences research

Published: November 26, 2016

GJA1 gene variations in sudden unexplained nocturnal death syndrome in the Chinese Han population.

GJA1 gene variations in sudden unexplained nocturnal death syndrome in the Chinese Han population.

Journal: Forensic science international

Published: September 12, 2016

Showing 1-12 of 16

Last Updated: 09/26/2026