Feng Zhang

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 35

Top Venues

Journal of medical genetics

Nature medicine

Nature communications

Human mutation

Sperm Bank of Fudan University

Fudan University (PHD)

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

Affiliation History

Sperm Bank of Fudan University

China

Director

State Key Laboratory of Genetic Engineering

China

Deputy Director

Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases

China

Deputy Director

Fudan University

China

Professor of Genetics

Fudan University

China

Associate Professor of Genetics

Baylor College of Medicine

United States

Postdoctoral Associate :: Department of Molecular and Human Genetics

Education History

Fudan University

China

PHD

East China University of Science and Technology

China

BSC

Publications

Hanni Ke, Shu-Yan Tang, Ting Guo, Dong Hou, Xue Jiao, Shan Li, Wei Luo, Bingying Xu, Shidou Zhao, Guangyu Li, Xiaoxi Zhang, Shuhua Xu, Lingbo Wang, Yanhua Wu, Jiucun Wang, Feng Zhang, Yingying Qin, Li Jin, Zi-Jiang Chen
Landscape of pathogenic mutations in premature ovarian insufficiency. Nature medicine 29 (2) (2023)
Hanni Ke, Shu-Yan Tang, Ting Guo, Dong Hou, Xue Jiao, Shan Li, Wei Luo, Bingying Xu, Shidou Zhao, Guangyu Li, Xiaoxi Zhang, Shuhua Xu, Lingbo Wang, Yanhua Wu, Jiucun Wang, Feng Zhang, Yingying Qin, Li Jin, Zi-Jiang Chen
Landscape of pathogenic mutations in premature ovarian insufficiency. Nature medicine (2023)
Shixiong Tian, Chaofeng Tu, Xiao-Jin He, Lanlan Meng, Jiaxiong Wang, Shuyan Tang, Yang Gao, Chunyu Liu, Huan Wu, Yiling Zhou, Mingrong Lv, Jing Guo, Li Jin, Yunxia Cao, Dongdong Tang, Feng Zhang, Yue-Qiu Tan
Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA. Journal of medical genetics (2023)
Hanni Ke, Shu-Yan Tang, Ting Guo, Dong Hou, Xue Jiao, Shan Li, Wei Luo, Bingying Xu, Shidou Zhao, Guangyu Li, Xiaoxi Zhang, Shuhua Xu, Lingbo Wang, Yanhua Wu, Jiucun Wang, Feng Zhang, Yingying Qin, Li Jin, Zi-Jiang Chen
Landscape of pathogenic mutations in premature ovarian insufficiency. Nature medicine 29 (2) (2023)
Hanni Ke, Shu-Yan Tang, Ting Guo, Dong Hou, Xue Jiao, Shan Li, Wei Luo, Bingying Xu, Shidou Zhao, Guangyu Li, Xiaoxi Zhang, Shuhua Xu, Lingbo Wang, Yanhua Wu, Jiucun Wang, Feng Zhang, Yingying Qin, Li Jin, Zi-Jiang Chen
Landscape of pathogenic mutations in premature ovarian insufficiency. Nature medicine 29 (2) (2023)
Sarah Kimmins, Richard A Anderson, Christopher L R Barratt, Hermann M Behre, Sarah R Catford, Christopher J De Jonge, Géraldine Delbes, Michael L Eisenberg, Nicolás Garrido, Brendan J Houston, Niels Jørgensen, Csilla Krausz, Ariane Lismer, Robert I McLachlan, Suks Minhas, Tim Moss, Allan A Pacey, Laerke Priskorn, Stefan Schlatt, Jacquetta Trasler, Leonardo Trasande, Frank Tüttelmann, Mónica Hebe Vazquez-Levin, Joris A Veltman, Feng Zhang, Brendan J Houston
Frequency, morbidity and equity - the case for increased research on male fertility. Nature reviews. Urology (2023)
Hanni Ke, Shu-Yan Tang, Ting Guo, Dong Hou, Xue Jiao, Shan Li, Wei Luo, Bingying Xu, Shidou Zhao, Guangyu Li, Xiaoxi Zhang, Shuhua Xu, Lingbo Wang, Yanhua Wu, Jiucun Wang, Feng Zhang, Yingying Qin, Li Jin, Zi-Jiang Chen
Landscape of pathogenic mutations in premature ovarian insufficiency. Nature medicine 29 (2) (2023)
Hanni Ke, Shu-Yan Tang, Ting Guo, Dong Hou, Xue Jiao, Shan Li, Wei Luo, Bingying Xu, Shidou Zhao, Guangyu Li, Xiaoxi Zhang, Shuhua Xu, Lingbo Wang, Yanhua Wu, Jiucun Wang, Feng Zhang, Yingying Qin, Li Jin, Zi-Jiang Chen
Landscape of pathogenic mutations in premature ovarian insufficiency. Nature medicine 29 (2) (2023)
Yue Qin, Yasong Du, Liqiang Chen, Yanyan Liu, Wenjing Xu, Ying Liu, Ying Li, Jing Leng, Yalan Wang, Xiao-Yong Zhang, Jianfeng Feng, Feng Zhang, Li Jin, Zi-Long Qiu, Xiaohong Gong, Hong-Yan Wang
A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling. Molecular psychiatry 27 (7) (2022)
Qian Zhang, Chengqiu Tao, Shuchang Gao, Shan Li, Bingying Xu, Hanni Ke, Yiyang Wang, Feng Zhang, Yingying Qin, Ling Zhang, Ting Guo
Homozygous Variant in KASH5 Causes Premature Ovarian Insufficiency by Disordered Meiotic Homologous Pairing. The Journal of clinical endocrinology and metabolism 107 (9) (2022)
Jintao Zhang, Xiaojin He, Huan Wu, Xin Zhang, Shenmin Yang, Chunyu Liu, Siyu Liu, Rong Hua, Shushu Zhou, Shuqin Zhao, Fan Hu, Junqiang Zhang, Wangjie Liu, Huiru Cheng, Yang Gao, Feng Zhang, Yunxia Cao, Mingxi Liu
Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse. Human molecular genetics 30 (21) (2022)
Xueguang Zhang, Lingbo Wang, Yongyi Ma, Yan Wang, Hongqian Liu, Mohan Liu, Lang Qin, Jinghong Li, Chuan Jiang, Xiaojian Zhang, Xudong Shan, Yuliang Liu, Jinsong Li, Yaqian Li, Rui Zheng, Yongkang Sun, Jianfeng Sun, Xiangyou Leng, Yan Liang, Feng Zhang, XiaoHui Jiang, Yihong Yang, Ying Shen
CEP128 is involved in spermatogenesis in humans and mice. Nature communications 13 (1) (2022)
Zixue Zhou, Xi Yang, Yuncheng Pan, Lingyue Shang, Siyuan Chen, Jialin Yang, Li Jin, Feng Zhang, Yanhua Wu
Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging. Human molecular genetics 30 (21) (2022)
Chunyu Liu, Ying Shen, Shuyan Tang, Jiaxiong Wang, Yiling Zhou, Shixiong Tian, Huan Wu, Jiangshan Cong, Xiao-Jin He, Li Jin, Yunxia Cao, Yihong Yang, Feng Zhang
Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility. Journal of medical genetics (2022)
Chengzhe Tao, Yuna Huang, Xuzhao Huang, Zhi Li, Yun Fan, Yan Zhang, Tingya Wan, Liyu Lu, Qiaoqiao Xu, Wei Wu, Di Wu, Feng Zhang, Chuncheng Lu
Association between Blood Manganese Levels and Visceral Adipose Tissue in the United States: A Population-Based Study. Nutrients 14 (22) (2022)
Qiqi Wang, Qing Chen, Yixin Zhang, Xue Zhang, Chunyu Liu, Daqi Wang, Yanhua Wu, Yixi Sun, Ling Zhang, Chengcheng Song, Yongming Wang, Yanpeng An, Huiru Tang, Congjian Xu, Yanting Wu, Li Jin, Hefeng Huang, Feng Zhang
HSD17B12 dosage insufficiency induced premature ovarian insufficiency in humans and mice. Clinical and translational medicine 12 (2) (2022)
Jiangshan Cong, Yihong Yang, Xin Wang, Ying Shen, Hui-Tao Qi, Chunyu Liu, Shuyan Tang, Sixian Wu, Shixiong Tian, Yiling Zhou, Xiaojin He, Lingbo Wang, Mo-Fang Liu, Feng Zhang
Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis. Cell discovery 8 (1) (2022)
Chunyu Liu, Ying Shen, Qunshan Shen, Wen Zhang, Jiaxiong Wang, Shu-Yan Tang, Huan Wu, Shixiong Tian, Jiangshan Cong, Xiaojin He, Li Jin, Feng Zhang, Xiaohui Jiang, Yunxia Cao
Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility. Cells 10 (7) (2021)
Jiangshan Cong, Xiong Wang, Amir Amiri-Yekta, Lingbo Wang, Zine-Eddine Kherraf, Chunyu Liu, Caroline Cazin, Shuyan Tang, Seyedeh Hanieh Hosseini, Shixiong Tian, Abbas Daneshipour, Jiaxiong Wang, Yiling Zhou, Yuyan Zeng, Shenmin Yang, Xiao-Jin He, Jinsong Li, Yunxia Cao, Li Jin, Pierre F Ray, Feng Zhang
Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice. Journal of medical genetics (2021)
Guoqing Li, Xi Yang, Lingbo Wang, Yuncheng Pan, Siyuan Chen, Lingyue Shang, Yicheng Zhang, Yucheng Wu, Zixue Zhou, Qing Chen, Xue Zhang, Ling Zhang, Yingchen Wang, Jinsong Li, Li Jin, Yanhua Wu, Xiaojin Zhang, Feng Zhang
Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice. Journal of medical genetics (2021)
Jianhong Ye, Youli Tong, Jiashun Lv, Rui Peng, Shuxia Chen, Lele Kuang, Ke Su, Yu-Fang Zheng, Ting Zhang, Feng Zhang, Li Jin, Xueyan Yang, Hongyan Wang
Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects. Human mutation 41 (8) (2020)
Mingrong Lv, Wangjie Liu, Wangfei Chi, Xiaoqing Ni, Jiajia Wang, Huiru Cheng, Wei-Yu Li, Shenmin Yang, Huan Wu, Junqiang Zhang, Yang Gao, Chunyu Liu, Caihua Li, Chenyu Yang, Qing Tan, Dongdong Tang, Jingjing Zhang, Bing Song, Yu-Jie Chen, Qiang Li, Yading Zhong, Zhihua Zhang, Hexige Saiyin, Li Jin, Yuping Xu, Ping Zhou, Zhaolian Wei, Chuanmao Zhang, Xiao-Jin He, Feng Zhang, Yunxia Cao
Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF. Journal of medical genetics 57 (7) (2020)
Chencheng Yao, Chao Yang, Liangyu Zhao, Peng Li, Ruhui Tian, Huixing Chen, Ying Guo, Yuhua Huang, Erlei Zhi, Jing Zhai, Hongfang Sun, Jianxiong Zhang, Yan Hong, Li Zhang, Zhiyong Ji, Feng Zhang, Zhi Zhou, Zheng Li
Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia. Journal of medical genetics 58 (10) (2020)
Ai-Jie Xin, Ronggui Qu, Guowu Chen, Ling Zhang, Junling Chen, Chengqiu Tao, Jing Fu, Jianan Tang, Yanfei Ru, Ying Chen, Xiandong Peng, Huijuan Shi, Feng Zhang, Xiao-Xi Sun
Disruption in ACTL7A causes acrosomal ultrastructural defects in human and mouse sperm as a novel male factor inducing early embryonic arrest. Science advances 6 (35) (2020)
Sen Zhao, Yuanqiang Zhang, Weisheng Chen, Weiyu Li, Shengru Wang, Lianlei Wang, Yanxue Zhao, Mao Lin, Yongyu Ye, Jiachen Lin, Yu Zheng, Jiaqi Liu, Hengqiang Zhao, Zihui Yan, Yongxin Yang, Yingzhao Huang, Guanfeng Lin, Zefu Chen, Zhen Zhang, Sen Liu, Lichao Jin, Zhaoyang Wang, Jingdan Chen, Yuchen Niu, Xiaoxin Li, Yong Wu, Yipeng Wang, Renqian Du, Na Gao, Hong Zhao, Ying Yang, Ying Liu, Ye Tian, Wenli Li, Yu Zhao, Jia Liu, Bin Yu, Na Zhang, Keyi Yu, Xu Yang, Shugang Li, Yuan Xu, Jianhua Hu, Zhe Liu, Jianxiong Shen, Shuyang Zhang, Jianzhong Su, Anas M Khanshour, Yared H Kidane, Brandon Ramo, Jonathan J Rios, Pengfei Liu, V Reid Sutton, Jennifer E Posey, Zhihong Wu, Guixing Qiu, Carol A Wise, Feng Zhang, Jianguo Zhang, Nan Wu, null null
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS). Journal of medical genetics 58 (1) (2020)
Ying Shen, Feng Zhang, Fuping Li, Xiaohui Jiang, Yihong Yang, Xiaoliang Li, Weiyu Li, Xiang Wang, Juan Cheng, Mohan Liu, Xueguang Zhang, Guiping Yuan, Xue Pei, Kailai Cai, Fengyun Hu, Jianfeng Sun, Lanzhen Yan, Li Tang, Chuan Jiang, Wenling Tu, Jinyan Xu, Haojuan Wu, Weiqi Kong, Shuying Li, Ke Wang, Kai Sheng, Xudong Zhao, Huanxun Yue, Xiaoyu Yang, Wenming Xu
Author Correction: Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella. Nature communications 10 (1) (2019)
Weiyu Li, Huan Wu, Fuping Li, Shixiong Tian, Zine-Eddine Kherraf, Jintao Zhang, Xiaoqing Ni, Mingrong Lv, Chunyu Liu, Qing Tan, Ying Shen, Amir Amiri-Yekta, Caroline Cazin, Jingjing Zhang, Wangjie Liu, Yan Zheng, Huiru Cheng, Yingbi Wu, Jiajia Wang, Yang Gao, Yujie Chen, Xiaomin Zha, Li Jin, Mingxi Liu, Xiao-Jin He, Pierre F Ray, Yunxia Cao, Feng Zhang
Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice. Journal of medical genetics 57 (2) (2019)
Lingbo Wang, Ying Zhang, Xiaoyi Fu, Shuangshuang Dong, Shuyan Tang, Ning Zhang, Chengcheng Song, Nan Yang, Lin Zhang, Hongyan Wang, Huijuan Shi, Li Jin, Feng Zhang, Jinsong Li, Keqin Hua
Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies. Cell research 30 (1) (2019)
Xiaojun Ren, Nan Yang, Nan Wu, Ximing Xu, Weisheng Chen, Ling Zhang, Yingping Li, Ren-Qian Du, Shuangshuang Dong, Sen Zhao, Shuxia Chen, Li-Ping Jiang, Lianlei Wang, Jianguo Zhang, Zhihong Wu, Li Jin, Guixing Qiu, James R Lupski, Jiangang Shi, Feng Zhang, Pengfei Liu
Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice. Journal of medical genetics 57 (6) (2019)
Ying Shen, Feng Zhang, Fuping Li, Xiaohui Jiang, Yihong Yang, Xiaoliang Li, Weiyu Li, Xiang Wang, Juan Cheng, Mohan Liu, Xueguang Zhang, Guiping Yuan, Xue Pei, Kailai Cai, Fengyun Hu, Jianfeng Sun, Lanzhen Yan, Li Tang, Chuan Jiang, Wenling Tu, Jinyan Xu, Haojuan Wu, Weiqi Kong, Shuying Li, Ke Wang, Kai Sheng, Xudong Zhao, Huanxun Yue, Xiaoyu Yang, Wenming Xu
Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella. Nature communications 10 (1) (2019)
Chunyu Liu, Mingrong Lv, Xiao-Jin He, Yong Zhu, Amir Amiri-Yekta, Weiyu Li, Huan Wu, Zine-Eddine Kherraf, Wangjie Liu, Jingjing Zhang, Qing Tan, Shuyan Tang, Yong-Jun Zhu, Yading Zhong, Caihua Li, Shixiong Tian, Zhiguo Zhang, Li Jin, Pierre Ray, Feng Zhang, Yunxia Cao
Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility. Journal of medical genetics 57 (1) (2019)
Weisheng Chen, Jiachen Lin, Lianlei Wang, Xiaoxin Li, Sen Zhao, Jiaqi Liu, Zeynep C Akdemir, Yanxue Zhao, Renqian Du, Yongyu Ye, Xiaofei Song, Yuanqiang Zhang, Zihui Yan, Xinzhuang Yang, Mao Lin, Jianxiong Shen, Shengru Wang, Na Gao, Ying Yang, Ying Liu, Wenli Li, Jia Liu, Na Zhang, Xu Yang, Yuan Xu, Jianguo Zhang, Mauricio R Delgado, Jennifer E Posey, Guixing Qiu, Jonathan J Rios, Pengfei Liu, Carol A Wise, Feng Zhang, Zhihong Wu, James R. Lupski, Nan Wu
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease. Human mutation 41 (1) (2019)
Qiqi Wang, Da Li, Baozhu Cai, Qing Chen, Caihua Li, Yanhua Wu, Li Jin, Xiuxia Wang, Xiaojin Zhang, Feng Zhang
Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations. Human genetics 138 (1) (2019)
Shuangshuang Dong, Chunyan Wang, Xueping Li, Qian Shen, Xiaoyi Fu, Mingyan Wu, Chengcheng Song, Nan Yang, Yanhua Wu, Hongyan Wang, Li Jin, Hong Xu, Feng Zhang
Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract. Molecular genetics and genomics : MGG 294 (2) (2019)
Weiyu Li, Xiaojin He, Shenmin Yang, Chunyu Liu, Huan Wu, Wangjie Liu, Mingrong Lv, Dongdong Tang, Jing Tan, Shuyan Tang, Yujie Chen, Jiajia Wang, Zhiguo Zhang, Hongyan Wang, Li Jin, Feng Zhang, Yunxia Cao
Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility. Journal of human genetics 64 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Feng Zhang