Yu-han Guo
Shanghai, China
Last Updated: 09/26/2026
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Found 12 publications
KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.
Journal: Journal of the American Heart Association
Published: November 08, 2022
Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions.
Journal: Biology
Published: January 04, 2022
A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus.
Journal: Genetics and molecular biology
Published: November 30, 2021
PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.
Journal: Journal of the American Heart Association
Published: November 30, 2021
SOX7 loss-of-function variation as a cause of familial congenital heart disease.
Journal: American journal of translational research
Published: August 08, 2021
VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.
Journal: European journal of medical genetics
Published: July 30, 2021
Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.
Journal: Clinical chemistry and laboratory medicine
Published: August 29, 2020
A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block.
Journal: International heart journal
Published: July 10, 2020
ISL1 loss-of-function variation causes familial atrial fibrillation.
Journal: European journal of medical genetics
Published: January 18, 2020
Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
Journal: International heart journal
Published: July 11, 2017
HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
Journal: Pediatric cardiology
Published: August 15, 2016
Showing 1-12 of 12
Last Updated: 09/26/2026