| Title | Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia |
| Authors | Li, Zhiqiang Chen, Jianhua Yu, Hao He, Lin Xu, Yifeng Zhang, Dai Yi, Qizhong Li, Changgui Li, Xingwang Shen, Jiawei Song, Zhijian Ji, Weidong Wang, Meng Zhou, Juan Chen, Boyu Liu, Yahui Wang, Jiqiang Wang, Peng Yang, Ping Wang, Qingzhong Feng, Guoyin Liu, Benxiu Sun, Wensheng Li, Baojie He, Guang Li, Weidong Wan, Chunling Xu, Qi Li, Wenjin Wen, Zujia Liu, Ke Huang, Fang Ji, Jue Ripke, Stephan Yue, Weihua Sullivan, Patrick F. O'Donovan, Michael C. Shi, Yongyong |
| Affiliation | Qingdao Univ, Affiliated Hosp, Qingdao, Peoples R China. Qingdao Univ, Biomed Sci Inst, SJTU Bio X Inst, Qingdao Branch, Qingdao, Peoples R China. Shanghai Jiao Tong Univ, Minist Educ, Collaborat Innovat Ctr Brain Sci, Key Lab Genet Dev & Neuropsychiat Disorders,Bio X, Shanghai, Peoples R China. Shanghai Jiao Tong Univ, Inst Social Cognit & Behav Sci, Shanghai, Peoples R China. Shanghai Jiao Tong Univ, Inst Neuropsychiat Sci & Syst Biol Med, Shanghai, Peoples R China. Shanghai Jiao Tong Univ, Shanghai Mental Hlth Ctr, Shanghai Key Lab Psychot Disorders, Shanghai, Peoples R China. Tsinghua Univ, Sch Life Sci, Tsinghua Peking Joint Ctr Life Sci, Beijing, Peoples R China. Peking Univ, Hosp 6, Inst Mental Hlth, Beijing, Peoples R China. Jining Med Univ, Dept Psychiat, Jining, Peoples R China. Peking Univ, McGovern Inst Brain Res, Peking Tsinghua Joint Ctr Life Sci, PKU IDG, Beijing, Peoples R China. Xinjiang Med Univ, Teaching Hosp 1, Dept Psychiat, Urumqi, Peoples R China. Qingdao Univ, Shandong Prov Key Lab Metab Dis, Qingdao, Peoples R China. Qingdao Univ, Metab Dis Inst, Qingdao, Peoples R China. Changning Mental Hlth Ctr, Shanghai, Peoples R China. Wuhu Fourth Peoples Hosp, Wuhu, Peoples R China. Longquan Mt Hosp Guangxi Prov, Liuzhou, Peoples R China. Chinese Acad Med Sci, Inst Basic Med Sci, Natl Lab Med Mol Biol, Beijing, Peoples R China. Peking Union Med Coll, Beijing, Peoples R China. Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Boston, MA 02114 USA. Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA USA. Charite, Dept Psychiat & Psychotherapy, Berlin, Germany. Univ N Carolina, Dept Genet, Chapel Hill, NC USA. Univ N Carolina, Dept Psychiat, Chapel Hill, NC USA. Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden. Cardiff Univ, Sch Med, MRC Ctr Neuropsychiat Genet & Gen, Div Psychol Med & Clin Neurosci, Cardiff, S Glam, Wales. Qingdao Univ, Affiliated Hosp, Qingdao, Peoples R China. Shi, YY (reprint author), Qingdao Univ, Biomed Sci Inst, SJTU Bio X Inst, Qingdao Branch, Qingdao, Peoples R China. Shi, YY (reprint author), Shanghai Jiao Tong Univ, Minist Educ, Collaborat Innovat Ctr Brain Sci, Key Lab Genet Dev & Neuropsychiat Disorders,Bio X, Shanghai, Peoples R China. Shi, YY (reprint author), Shanghai Jiao Tong Univ, Inst Social Cognit & Behav Sci, Shanghai, Peoples R China. Shi, YY (reprint author), Shanghai Jiao Tong Univ, Inst Neuropsychiat Sci & Syst Biol Med, Shanghai, Peoples R China. Shi, YY (reprint author), Xinjiang Med Univ, Teaching Hosp 1, Dept Psychiat, Urumqi, Peoples R China. Shi, YY (reprint author), Changning Mental Hlth Ctr, Shanghai, Peoples R China. |
| Keywords | COMMON VARIANTS GENETIC-VARIATION CONFERRING RISK HAN CHINESE POPULATION DISEASE METAANALYSES PATHWAYS 6P22.1 IMMUNE |
| Issue Date | 2017 |
| Publisher | NATURE GENETICS |
| Citation | NATURE GENETICS. 2017, 49(11), 1576-+. |
| Abstract | We conducted a genome-wide association study (GWAS) with replication in 36,180 Chinese individuals and performed further transancestry meta-analyses with data from the Psychiatry Genomics Consortium (PGC2). Approximately 95% of the genome-wide significant (GWS) index alleles (or their proxies) from the PGC2 study were overrepresented in Chinese schizophrenia cases, including similar to 50% that achieved nominal significance and similar to 75% that continued to be GWS in the transancestry analysis. The Chinese-only analysis identified seven GWS loci; three of these also were GWS in the transancestry analyses, which identified 109 GWS loci, thus yielding a total of 113 GWS loci (30 novel) in at least one of these analyses. We observed improvements in the fine-mapping resolution at many susceptibility loci. Our results provide several lines of evidence supporting candidate genes at many loci and highlight some pathways for further research. Together, our findings provide novel insight into the genetic architecture and biological etiology of schizophrenia. |
| URI | http://hdl.handle.net/20.500.11897/497783 |
| ISSN | 1061-4036 |
| DOI | 10.1038/ng.3973 |
| Indexed | SCI(E) |
| Appears in Collections: | 第六医院 生命科学学院 |
