Yong Feng

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

Jia-Hui Xia, Chunyu Liu, Bei-sha Tang et al. · Nature Genetics · 1998 · 422 citations

Auditory Processing, Developmental Biology, Health Sciences +13

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

Denise Yan, Demet Tekin, Güney Bademci et al. · Human Genetics · 2016 · 136 citations · Full text

Allelic Variant, Multiple Continents, Mendelian Disorder +12

Up-regulation of CD44 in the development of metastasis, recurrence and drug resistance of ovarian cancer

Yan Gao, Rosemary Foster, Xiaoqian Yang et al. · Oncotarget · 2015 · 127 citations · Full text

Common genetic variants on 1p13.2 associate with risk of autism

Kun Xia, Hui Guo, Zhengmao Hu et al. · Molecular Psychiatry · 2013 · 106 citations

Syndromic Autism, Genetic Disorder, Genetics +7

<i>SLC39A5</i> mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia

Hui Guo, Xuemin Jin, Tengfei Zhu et al. · Journal of Medical Genetics · 2014 · 102 citations · Full text