P
Peng Zhang
Researcher at Beijing Genomics Institute
Publications - 10
Citations - 954
Peng Zhang is an academic researcher from Beijing Genomics Institute. The author has contributed to research in topics: Exome sequencing & Spinocerebellar ataxia. The author has an hindex of 6, co-authored 9 publications receiving 890 citations. Previous affiliations of Peng Zhang include Anhui Medical University & Chinese Ministry of Education.
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Journal ArticleDOI
Association analyses identify six new psoriasis susceptibility loci in the Chinese population
Liangdan Sun,Hui Cheng,Hui Cheng,Zaixing Wang,Zaixing Wang,Anping Zhang,Anping Zhang,Pei-Guang Wang,Pei-Guang Wang,Jinhua Xu,Qi-Xing Zhu,Qi-Xing Zhu,Hai-Sheng Zhou,Hai-Sheng Zhou,Eva Ellinghaus,Furen Zhang,Xiong-Ming Pu,Xueqin Yang,Jianzhong Zhang,Ai-E Xu,Ri-Na Wu,Limin Xu,Lin Peng,Cynthia Helms,Yunqing Ren,Yunqing Ren,Chi Zhang,Chi Zhang,Shu-Mei Zhang,Shu-Mei Zhang,Rajan P. Nair,Hongyan Wang,Hongyan Wang,Guo-Shu Lin,Guo-Shu Lin,Philip E. Stuart,Xing Fan,Xing Fan,Gang Chen,Gang Chen,Trilokraj Tejasvi,Pan Li,Pan Li,Jun Zhu,Jun Zhu,Zhi-Ming Li,Zhi-Ming Li,Hong-Mei Ge,Hong-Mei Ge,Michael Weichenthal,Wen-Zheng Ye,Wen-Zheng Ye,Cheng Zhang,Cheng Zhang,Songke Shen,Songke Shen,Baoqi Yang,Yuan-Yuan Sun,Yuan-Yuan Sun,Shan-Shan Li,Shan-Shan Li,Yan Lin,Yan Lin,Jian-Hua Jiang,Cun-Tao Li,Cun-Tao Li,Ri-Xin Chen,Ri-Xin Chen,Juan Cheng,Xin Jiang,Xin Jiang,Peng Zhang,Peng Zhang,Wei-Min Song,Jin Tang,Jin Tang,Hao-Qin Zhang,Hao-Qin Zhang,Li Sun,Jing Cui,Jing Cui,Li-Jun Zhang,Li-Jun Zhang,Biao Tang,Biao Tang,Fei Huang,Fei Huang,Qian Qin,Qian Qin,Xiao-Ping Pei,Xiao-Ping Pei,Ai-Min Zhou,Li-Mei Shao,Li-Mei Shao,Jian-Lan Liu,Jian-Lan Liu,Feng-Yu Zhang,Feng-Yu Zhang,Wei-Dong Du,Wei-Dong Du,Andre Franke,Anne M. Bowcock,James T. Elder,Jianjun Liu,Jianjun Liu,Jianjun Liu,Sen Yang,Sen Yang,Xuejun Zhang +108 more
TL;DR: Six new susceptibility loci associated with psoriasis in the Chinese study containing the candidate genes ERAP1, PTTG1, CSMD1, GJB2, SERPINB8 and ZNF816A are identified and the heterogeneity of disease susceptibility between the Chinese and European populations is highlighted.
Journal ArticleDOI
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing
Junling Wang,Xu Yang,Kun Xia,Zheng mao Hu,Ling Weng,Xin Jin,Hong Jiang,Peng Zhang,Lu Shen,Ji Feng Guo,Nan Li,Yingrui Li,Li fang Lei,Jie Zhou,Juan Du,Ya Fang Zhou,Qian Pan,Jing Wang,Jun Wang,Rui Qiang Li,Bei Sha Tang +20 more
TL;DR: The finding of TGM6 as a novel causative gene of spinocerebellar ataxia illustrates whole-exome sequencing of affected individuals from one family as an effective and cost efficient method for mapping genes of rare Mendelian disorders and the use of linkage analysis and exome sequencing for further improving efficiency.
Journal ArticleDOI
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.
Junling Wang,Li Cao,Xun-Hua Li,Zhengmao Hu,Jia-Da Li,Jianguo Zhang,Yu Liang,San-A,Nan Li,Su-Qin Chen,Jifeng Guo,Hong Jiang,Lu Shen,Lan Zheng,Xiao Mao,Weiqian Yan,Ying Zhou,Yuting Shi,Sanxi Ai,Mei-zhi Dai,Peng Zhang,Kun Xia,Sheng-Di Chen,Beisha Tang +23 more
TL;DR: Proline-rich transmembrane protein 2 (PRRT2) is identified as the first causative gene of paroxysmal kinesigenic dyskinesias by using a combination of exome sequencing and linkage analysis, warranting further investigations to understand the pathogenesis of this disorder.
Journal ArticleDOI
Confirmation by exome sequencing of the pathogenic role of NCSTN mutations in acne inversa (hidradenitis suppurativa).
Yuan Liu,Yuan Liu,Min Gao,Min Gao,Yong Mei Lv,Yong Mei Lv,Xu Yang,Yun Qing Ren,Yun Qing Ren,Tao Jiang,Xin Zhang,Xin Zhang,Bi Rong Guo,Bi Rong Guo,Min Li,Min Li,Qing Zhang,Peng Zhang,Fu Sheng Zhou,Fu Sheng Zhou,Gang Chen,Gang Chen,Xianyong Yin,Xianyong Yin,Xian Bo Zuo,Xian Bo Zuo,Liangdan Sun,Liangdan Sun,X. Zheng,X. Zheng,Shu Mei Zhang,Shu Mei Zhang,Jianjun Liu,Jianjun Liu,Youwen Zhou,Youwen Zhou,Yingrui Li,Jun Wang,Jian Wang,Huanming Yang,Sen Yang,Sen Yang,Rui Qiang Li,Xuejun Zhang,Xuejun Zhang +44 more
TL;DR: Exome capture was carried out using Agilent SureSelect Human All Exon Kit guided by the manufacturer’s protocols and paired-end sequencing was conducted according to Declaration of Helsinki principles.
Journal ArticleDOI
Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia.
Zi-xiong Zhan,Xinxin Liao,Juan Du,Yingying Luo,Zhaoting Hu,Junling Wang,Xinxiang Yan,Jianguo Zhang,Mei-zhi Dai,Peng Zhang,Kun Xia,Beisha Tang,Lu Shen +12 more
TL;DR: Exome sequencing can be used not only to find a novel causative gene, but also to quickly identify mutations of known genes when the clinical elements are etiologically misleading, this study suggests.