H
Hongyan Wang
Researcher at Fudan University
Publications - 117
Citations - 3320
Hongyan Wang is an academic researcher from Fudan University. The author has contributed to research in topics: Gene & Neural tube. The author has an hindex of 25, co-authored 98 publications receiving 2500 citations. Previous affiliations of Hongyan Wang include University of Pennsylvania & Boston Children's Hospital.
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Journal ArticleDOI
Genomic dissection of population substructure of Han Chinese and its implication in association studies.
Shuhua Xu,Xianyong Yin,Shilin Li,Wenfei Jin,Haiyi Lou,Ling Yang,Xiaohong Gong,Hongyan Wang,Yiping Shen,Yiping Shen,Xuedong Pan,Yungang He,Yajun Yang,Yi Wang,Wenqing Fu,Yu An,Jiucun Wang,Jingze Tan,Ji Qian,Xiaoli Chen,Xin Zhang,Yangfei Sun,Xuejun Zhang,Bai-Lin Wu,Bai-Lin Wu,Li Jin +25 more
TL;DR: Examination of population substructures in a diverse set of over 1700 Han Chinese samples collected from 26 regions across China showed that most differentiated genes among clusters are involved in cardiac arteriopathy, and signals indicating significant differences among Han Chinese subpopulations should be carefully explained.
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A Genome-Wide Search for Signals of High Altitude Adaptation in Tibetans
Shuhua Xu,Shilin Li,Yajun Yang,Jingze Tan,Haiyi Lou,Wenfei Jin,Ling Yang,Xuedong Pan,Jiucun Wang,Yiping Shen,Bai-Lin Wu,Bai-Lin Wu,Hongyan Wang,Li Jin,Li Jin +14 more
TL;DR: In this article, the authors conducted a genome-wide study of 1,000,000 genetic variants in 46 Tibetans and 92 Han Chinese (HAN) for identifying the signals of high-altitude adaptations (HAAs) in Tibetan genomes.
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Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis.
Jinbo B Fan,Chang Shun Zhang,Niu Fan Gu,Xing Wang Li,Wei Wei Sun,Hongyan Wang,Guo Yin Feng,David St Clair,Lin He,Lin He +9 more
TL;DR: The data provide minimal evidence that the Val allele is a susceptibility factor for schizophrenia in either European or Asian populations.
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Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella
Shuyan Tang,Xiong Wang,Xiong Wang,Weiyu Li,Xiaoyu Yang,Zheng Li,Wangjie Liu,Caihua Li,Zi-Jue Zhu,Lingxiang Wang,Jiaxiong Wang,Ling Zhang,Xiaoling Sun,Erlei Zhi,Hongyan Wang,Hong Li,Li Jin,Yang Luo,Jian Wang,Shenmin Yang,Feng Zhang +20 more
TL;DR: The authors' experimental observations on human subjects and animal models strongly suggest that biallelic mutations in either CFAP43 or CFAP44 can cause sperm flagellar abnormalities and impair sperm motility.
Journal ArticleDOI
Mutations in TUBB8 and Human Oocyte Meiotic Arrest
Ruizhi Feng,Qing Sang,Yanping Kuang,Xiaoxi Sun,Zheng Yan,Shaozhen Zhang,Juanzi Shi,Guoling Tian,Anna Luchniak,Yusuke Fukuda,Bin Li,Min Yu,Junling Chen,Yao Xu,Luo Guo,Ronggui Qu,Xueqian Wang,Zhaogui Sun,Miao Liu,Huijuan Shi,Hongyan Wang,Yi Feng,Ruijin Shao,Renjie Chai,Qiaoli Li,Qinghe Xing,Rui Zhang,Eva Nogales,Li Jin,Lin He,Mohan L. Gupta,Nicholas J. Cowan,Lei Wang +32 more
TL;DR: Seven mutations in the primate-specific gene TUBB8 that were responsible for oocyte meiosis I arrest in 7 of the 24 families have dominant-negative effects that disrupt microtubule behavior and oocytes meiotic spindle assembly and maturation, causing female infertility.