Zongzhe Q. Li

1095# Jiefang Ave
Wuhan, 430030, China

Last Updated: 09/26/2026

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Found 46 publications

Novel FLCN mutations in Birt-Hogg-Dubé patients and potential intervention of FLCN mRNA.

Novel FLCN mutations in Birt-Hogg-Dubé patients and potential intervention of FLCN mRNA.

Journal: Therapeutic advances in respiratory disease

Published: May 28, 2026

Varenicline and Ventricular Ectopy After Myocardial Infarction: A Randomized Phase 2 Study.

Varenicline and Ventricular Ectopy After Myocardial Infarction: A Randomized Phase 2 Study.

Journal: Journal of the American College of Cardiology

Published: November 30, 2025

Ultra-long-term follow-up of renal denervation in patients with resistant hypertension and mild chronic kidney disease

Ultra-long-term follow-up of renal denervation in patients with resistant hypertension and mild chronic kidney disease

Journal: Zhonghua xin xue guan bing za zhi

Published: October 26, 2025

A rare case of fulminant myocarditis complicated with thrombotic aorta occlusion and multiple thrombosis: a case report.

A rare case of fulminant myocarditis complicated with thrombotic aorta occlusion and multiple thrombosis: a case report.

Journal: Frontiers of medicine

Published: April 04, 2025

EMB is essential for enteric nervous system development mediated by PI3K signaling.

EMB is essential for enteric nervous system development mediated by PI3K signaling.

Journal: Genome medicine

Published: January 17, 2025

FBN2 pathogenic variants in congenital contractural arachnodactyly with severe cardiovascular manifestations.

FBN2 pathogenic variants in congenital contractural arachnodactyly with severe cardiovascular manifestations.

Journal: Connective tissue research

Published: April 11, 2024

A Compound Heterozygous Pathogenic Variant in ZP2 Gene Causes Female Infertility.

A Compound Heterozygous Pathogenic Variant in ZP2 Gene Causes Female Infertility.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: November 20, 2023

Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report.

Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report.

Journal: BMC medical genomics

Published: November 10, 2023

Naringenin inhibits thoracic aortic aneurysm formation in mice with Marfan syndrome

Naringenin inhibits thoracic aortic aneurysm formation in mice with Marfan syndrome

Journal: Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

Published: October 14, 2022

FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review.

FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review.

Journal: Genes

Published: September 02, 2022

Machine learning modeling identifies hypertrophic cardiomyopathy subtypes with genetic signature.

Machine learning modeling identifies hypertrophic cardiomyopathy subtypes with genetic signature.

Journal: Frontiers of medicine

Published: July 25, 2022

A laboratory viewpoint of the consensus paper from the European Society of Cardiology regarding the utilization of the American College of Medical Genetics and Genomics pathogenic criteria for cardiomyopathy.

A laboratory viewpoint of the consensus paper from the European Society of Cardiology regarding the utilization of the American College of Medical Genetics and Genomics pathogenic criteria for cardiomyopathy.

Journal: European heart journal

Published: May 22, 2022

Showing 1-12 of 46

Last Updated: 09/26/2026