J. Wen

发表

Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL

Hongbo Xu, H. Deng, S. Deng, 2019, Neurodegenerative Diseases.

A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Development

Yong Feng, L. Mei, Chufeng He, 2021, Frontiers in Cell and Developmental Biology.

Fishtail phenomenon in Ho-added PMP YBCO

Lei Shi, N. Koshizuka, Lian Zhou, 1998 .

Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families

Yong Feng, Shu-shan Sang, L. Mei, 2020, European Archives of Oto-Rhino-Laryngology.

Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation.

Yong Feng, L. Mei, Hongsheng Chen, 2021, Stem cell research.

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

Yong Feng, Jing Liu, Shu-shan Sang, 2019, Front. Genet..

A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review.

X. Liu, Yong Feng, Jing Liu, 2019, Gene.

A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family

Yong Feng, Shu-shan Sang, Zhijie Niu, 2018, Journal of Human Genetics.

Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.

M. Li, Yong Feng, Shu-shan Sang, 2018, International journal of pediatric otorhinolaryngology.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.

Novel Compound Heterozygous PRKN Variants in a Han-Chinese Family with Early-Onset Parkinson's Disease

Chengyuan Song, H. Deng, P. Hu, 2019, Parkinson's disease.

Novel CompoundHeterozygousPRKNVariants in aHan-Chinese Family with Early-Onset Parkinson’s Disease

Chengyuan Song, H. Deng, P. Hu, 2019 .

An artificial intelligence network‐guided signature for predicting outcome and immunotherapy response in lung adenocarcinoma patients based on 26 machine learning algorithms

Q. Cheng, Xizhe Li, Jian Zhang, 2023, Cell proliferation.

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

Yong Feng, L. Mei, Chufeng He, 2023, Pigment Cell & Melanoma Research.

Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation.

Yong Feng, Jing Liu, L. Mei, 2021, Stem cell research.

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

Yong Feng, L. Mei, Jie Sun, 2023, PloS one.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

X. Liu, M. Li, D. Yan, 2018, Human Genetics.