Yong Feng

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Topics

Spectrum Disorder

Antiretroviral Therapy

Circulating Tumor

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Human molecular genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Jie Wen, Jian Song, Jiale Chen, Zhili Feng, Qiancheng Jing, Wei Gong, Xiaoming Kang, Lingyun Mei, Chufeng He, Lu Ma, Yong Feng
Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway in iPS-derived melanocytes. Pigment cell & melanoma research (2023)
Xianlin Liu, Jie Wen, Xuezhong Liu, Anhai Chen, Sijun Li, Jing Liu, Jie Sun, Wei Gong, Xiaoming Kang, Zhili Feng, Chufeng He, Lingyun Mei, Jie Ling, Yong Feng
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. PloS one 18 (9) (2023)
Sida Huang, Lu Ma, Xuezhong Liu, Chufeng He, Jiada Li, Zhengmao Hu, Lu Jiang, Yalan Liu, Xianlin Liu, Yong Feng, Xinzhang Cai
A non-coding variant in 5' untranslated region drove up-regulation of Pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans. Human molecular genetics (2022)
Minwoo Wendy Jang, Doo-Yi Oh, Eunyoung Yi, Xuezhong Liu, Jie Ling, Nayoung Kim, Kushal Sharma, Tai Young Kim, Seungmin Lee, Ah-Reum Kim, Min Young Kim, Min-A Kim, Mingyu Lee, Jin-Hee Han, Jae Joon Han, Hye-Rim Park, Bong Jik Kim, Sang-Yeon Lee, Dong Ho Woo, Jayoung Oh, Soo-Jin Oh, Tingting Du, Ja-Won Koo, Seung-Ha Oh, Hyun-Woo Shin, Moon-Woo Seong, Kyu-Yup Lee, Un-Kyung Kim, Jung Bum Shin, Shushan Sang, Xinzhang Cai, Lingyun Mei, Chufeng He, Susan Halloran Blanton, Zheng-Yi Chen, Hongsheng Chen, Xianlin Liu, Aida Nourbakhsh, Zaohua Huang, Kwon-Woo Kang, Woong-Yang Park, Yong Feng, Justin Daho Lee, Byung Yoon Choi
A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder. Proceedings of the National Academy of Sciences of the United States of America 118 (22) (2021)
Sida Huang, Jian Song, Chufeng He, Xinzhang Cai, Kai Yuan, Lingyun Mei, Yong Feng
Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome. Gene therapy (2021)
Meng Li, Lingyun Mei, Chufeng He, Hongsheng Chen, Xinzhang Cai, Yalan Liu, Runyi Tian, Qi Tian, Jian Song, Lu Jiang, Chang Liu, Hong Wu, Taoxi Li, Jing Liu, Ximan Li, Yifang Yi, Denise Yan, Susan H Blanton, Zhengmao Hu, Xuezhong Liu, Jiada Li, Jie Ling, Yong Feng
Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (2019)
Wu Li, Lingyun Mei, Hongsheng Chen, Xinzhang Cai, Yalan Liu, Meichao Men, Xue Zhong Liu, Denise Yan, Jie Ling, Yong Feng
New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing. Neural plasticity 2019 (2019)