Yufeng Huang

Wuhan, China

Last Updated: 09/26/2026

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Found 16 publications

A male patient with atrial myxoma and multiple metastatic intracranial aneurysms: A case report and literature review.

A male patient with atrial myxoma and multiple metastatic intracranial aneurysms: A case report and literature review.

Journal: The Journal of international medical research

Published: April 25, 2025

Identification of a new gain-of-function variant p.N536Y of KCNMA1 associated with PNKD3 in the Chinese population.

Identification of a new gain-of-function variant p.N536Y of KCNMA1 associated with PNKD3 in the Chinese population.

Journal: Acta physiologica (Oxford, England)

Published: March 10, 2025

A novel USP27X missense variant identified in an individual with intellectual disability.

A novel USP27X missense variant identified in an individual with intellectual disability.

Journal: Journal of human genetics

Published: August 22, 2024

Analysis of epilepsy-associated variants in HCN3 - Functional implications and clinical observations.

Analysis of epilepsy-associated variants in HCN3 - Functional implications and clinical observations.

Journal: Epilepsia open

Published: March 19, 2024

Identification and Characterization of a Germline Mutation in CARD11 From a Chinese Case of B Cell Expansion With NF-κB and T Cell Anergy.

Identification and Characterization of a Germline Mutation in CARD11 From a Chinese Case of B Cell Expansion With NF-κB and T Cell Anergy.

Journal: Frontiers in immunology

Published: March 05, 2021

Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spams.

Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spams.

Journal: Neurogenetics

Published: May 08, 2019

Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardia.

Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardia.

Journal: Molecular genetics and genomics : MGG

Published: September 30, 2018

Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillation.

Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillation.

Journal: Annals of human genetics

Published: August 06, 2018

Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation.

Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation.

Journal: Scientific reports

Published: August 31, 2017

Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease.

Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease.

Journal: Scientific reports

Published: July 18, 2016

Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.

Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.

Journal: Atherosclerosis

Published: June 26, 2015

Elevated serum chloride is an independent risk factor for coronary heart disease: A retrospective study of more than 13,000 Han Chinese.

Elevated serum chloride is an independent risk factor for coronary heart disease: A retrospective study of more than 13,000 Han Chinese.

Journal: International journal of cardiology

Published: June 16, 2015

Showing 1-12 of 16

Last Updated: 09/26/2026