Yong Feng

8PUBLICATIONS
23CO-AUTHORS
Genetic immunologyEpigenetics (incl. genome methylation and epigenomics)MechanobiologyNeurogeneticsCancer genetics
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Publications (8)

|Jun 17, 2025
The γ-Actin with pathogenic variants of sites on actin-binding proteins caused earlier onset and more malignant progressive hearing loss.

Sijun Li, Qi Feng, Lingyun Mei

|Sep 14, 2023
Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss.

Xianlin Liu, Jie Wen, Xuezhong Liu

|Aug 10, 2023
Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway in iPS-derived melanocytes.

Jie Wen, Jian Song, Jiale Chen

|Sep 01, 2022
A non-coding variant in 5' untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans.

Sida Huang, Lu Ma, Xuezhong Liu

|May 29, 2021
A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder.

Minwoo Wendy Jang, Doo-Yi Oh, Eunyoung Yi

|Feb 26, 2021
Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome.

Sida Huang, Jian Song, Chufeng He

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Frequent Collaborators

3 joint publications

Lingyun Mei

2 joint publications

Jie Ling

2 joint publications

Sida Huang

1 joint publications

Meichao Men