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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia
Authors:Shi Yongyong  Li Zhiqiang  Xu Qi  Wang Ti  Li Tao  Shen Jiawei  Zhang Fengyu  Chen Jianhua  Zhou Guoquan  Ji Weidong  Li Baojie  Xu Yifeng  Liu Dengtang  Wang Peng  Yang Ping  Liu Benxiu  Sun Wensheng  Wan Chunling  Qin Shengying  He Guang  Steinberg Stacy  Cichon Sven  Werge Thomas  Sigurdsson Engilbert  Tosato Sarah  Palotie Aarno  Nöthen Markus M  Rietschel Marcella  Ophoff Roel A  Collier David A  Rujescu Dan  Clair David St  Stefansson Hreinn  Stefansson Kari  Ji Jue  Wang Qingzhong  Li Wenjin  Zheng Linqing  Zhang Hairong  Feng Guoyin  He Lin
Institution:Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, China. shiyongyong@gmail.com
Abstract:Schizophrenia is a severe mental disorder affecting ~1% of the world population, with heritability of up to 80%. To identify new common genetic risk factors, we performed a genome-wide association study (GWAS) in the Han Chinese population. The discovery sample set consisted of 3,750 individuals with schizophrenia and 6,468 healthy controls (1,578 cases and 1,592 controls from northern Han Chinese, 1,238 cases and 2,856 controls from central Han Chinese, and 934 cases and 2,020 controls from the southern Han Chinese). We further analyzed the strongest association signals in an additional independent cohort of 4,383 cases and 4,539 controls from the Han Chinese population. Meta-analysis identified common SNPs that associated with schizophrenia with genome-wide significance on 8p12 (rs16887244, P = 1.27 × 10(-10)) and 1q24.2 (rs10489202, P = 9.50 × 10(-9)). Our findings provide new insights into the pathogenesis of schizophrenia.
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