Huijun Wang

20PUBLICATIONS
12CO-AUTHORS
Forensic epidemiologyNeonatologyGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Gene mapping
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (20)

|May 25, 2026
Loss-of-function variants in EPHX3 cause nonsyndromic epidermal differentiation disorders.

|Jul 25, 2025
Gain-of-function variant in NNT causes premature diffuse familial sebaceous hyperplasia.

Lina Liang, Sheng Wang, Shimiao Huang

|Feb 19, 2025
Variants in KLF4 affecting residue Asp441 cause an autosomal dominant syndromic ichthyosis.

Zijuan Wang, Jun Liu, Oded Wechsberg

|Jul 15, 2024
A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataracts.

Huijun Wang, Yuan Wu, Jennifer A Bassetti

|Mar 15, 2024
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation.

Xingyuan Jiang, Chao Yang, Zhaoyang Wang

|Jan 23, 2023
Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder.

Zhuoqing Gong, Shangzhi Dai, Xingyuan Jiang

Pageof 4

Frequent Collaborators

9 joint publications

Zhimiao Lin

9 joint publications

Zhimiao Lin

4 joint publications

Zhuoqing Gong

2 joint publications

Fang Yang