Yufeng F. Huang

Wuhan, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Journal: Frontiers in genetics

Published: May 09, 2026

Integrative network toxicology and molecular docking preliminarily explore the potential role of polystyrene microplastics in childhood obesity.

Integrative network toxicology and molecular docking preliminarily explore the potential role of polystyrene microplastics in childhood obesity.

Journal: SAR and QSAR in environmental research

Published: February 24, 2026

TPM1-p.E181K mutation suppresses CaMKII/HDAC4 signaling pathway leading to pediatric restrictive cardiomyopathy.

TPM1-p.E181K mutation suppresses CaMKII/HDAC4 signaling pathway leading to pediatric restrictive cardiomyopathy.

Journal: Frontiers in genetics

Published: June 30, 2025

Clinical and genetic characterization of congenital disorders of glycosylation in 20 Chinese patients.

Clinical and genetic characterization of congenital disorders of glycosylation in 20 Chinese patients.

Journal: Orphanet journal of rare diseases

Published: January 10, 2025

Detection of inversion with breakpoints in ARSB causing MPS VI by whole-genome sequencing: lessons learned and best practices.

Detection of inversion with breakpoints in ARSB causing MPS VI by whole-genome sequencing: lessons learned and best practices.

Journal: Frontiers in genetics

Published: June 21, 2024

A case of restrictive cardiomyopathy associated with new TPM1 gene mutation

A case of restrictive cardiomyopathy associated with new TPM1 gene mutation

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: October 08, 2022

Identification and characterization of a new variation in DPM2 gene in two Chinese siblings with mild intellectual impairment.

Identification and characterization of a new variation in DPM2 gene in two Chinese siblings with mild intellectual impairment.

Journal: Frontiers in genetics

Published: April 28, 2022

A novel variant in the HX repeat motif of ATN1 in a Chinese patient with CHEDDA syndrome and literature review.

A novel variant in the HX repeat motif of ATN1 in a Chinese patient with CHEDDA syndrome and literature review.

Journal: Molecular genetics & genomic medicine

Published: March 18, 2022

miR-190a-5p Partially Represses the Abnormal Electrical Activity of SCN3B in Cardiac Arrhythmias by Downregulation of IL-2.

miR-190a-5p Partially Represses the Abnormal Electrical Activity of SCN3B in Cardiac Arrhythmias by Downregulation of IL-2.

Journal: Frontiers in cardiovascular medicine

Published: October 26, 2021

Infantile-onset CMT2D/dSMA-V in a Chinese family with parental germline mosaicism for a novel mutation in the GARS1 gene.

Infantile-onset CMT2D/dSMA-V in a Chinese family with parental germline mosaicism for a novel mutation in the GARS1 gene.

Journal: Molecular genetics & genomic medicine

Published: August 23, 2021

Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann-Steiner syndrome.

Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann-Steiner syndrome.

Journal: Molecular genetics & genomic medicine

Published: March 10, 2021

A 9-month-old Chinese patient with Gabriele-de Vries syndrome due to novel germline mutation in the YY1 gene.

A 9-month-old Chinese patient with Gabriele-de Vries syndrome due to novel germline mutation in the YY1 gene.

Journal: Molecular genetics & genomic medicine

Published: May 07, 2020

Showing 1-12 of 15

Last Updated: 09/26/2026