Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese

Biological Psychiatry

Volumn 80, Issue 4, 2016, Pages 331-337

  Li, Zhiqiang ^a   Chen, Jianhua ^a,b   Xu, Yifeng ^b   Yi, Qizhong ^c   Ji, Weidong ^a,d   Wang, Peng ^e   Shen, Jiawei ^a   Song, Zhijian ^a   Wang, Meng ^a   Yang, Ping ^e   Wang, Qingzhong ^a   Feng, Guoyin ^b   Liu, Benxiu ^f   Sun, Wensheng ^f   Xu, Qi ^g   Li, Baojie ^a   He, Lin ^a,h   He, Guang ^a   Li, Wenjin ^a   Wen, Zujia ^a   Liu, Ke ^a   Huang, Fang ^a   Zhou, Juan ^a   Ji, Jue ^a   Li, Xingwang ^a   Shi, Yongyong ^a,b,c,d,i   more..

^a SHANGHAI JIAO TONG UNIVERSITY   (China)

^b SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

^c First Teaching Hospital of Xinjiang Medical University   (United States)

^d Changning Mental Health Center   (China)

^e Wuhu Fourth People's Hospital   (United States)

^f Longquan Mountain Hospital of Guangxi Province   (United States)

^g INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

^h FUDAN UNIVERSITY   (China)

ⁱ QINGDAO UNIVERSITY   (China)

Author keywords

10p12.1; 13q13.3; 1p36.32; Copy number variation; Han Chinese; Schizophrenia

Indexed keywords

ARHGEF16 PROTEIN; MEGF6 PROTEIN; MIR551A PROTEIN; NEUROPEPTIDE RECEPTOR; NRXN1 PROTEIN; PRDM16 PROTEIN; PROTEIN; UNCLASSIFIED DRUG; VIPR 2 PROTEIN; NERVE CELL ADHESION MOLECULE; NERVE PROTEIN; NRXN1 PROTEIN, HUMAN; VASOACTIVE INTESTINAL POLYPEPTIDE RECEPTOR 2; VIPR2 PROTEIN, HUMAN;

ARTICLE; CHINESE; CLINICAL EVALUATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DISEASE ASSOCIATION; GENE DELETION; GENE DUPLICATION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOME-WIDE ASSOCIATION STUDY; HAN CHINESE; HAPPY PUPPET SYNDROME; HUMAN; MAJOR CLINICAL STUDY; POPULATION; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RISK ASSESSMENT; RISK FACTOR; SCHIZOPHRENIA; WILLIAMS BEUREN SYNDROME; ASIAN CONTINENTAL ANCESTRY GROUP; CHROMOSOME DISORDER; ETHNOLOGY; FEMALE; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; MALE;

ASIAN CONTINENTAL ANCESTRY GROUP; CELL ADHESION MOLECULES, NEURONAL; CHROMOSOME DISORDERS; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; MALE; NERVE TISSUE PROTEINS; RECEPTORS, VASOACTIVE INTESTINAL PEPTIDE, TYPE II; SCHIZOPHRENIA;

EID: 84969913403     PISSN: 00063223     EISSN: 18732402     Source Type: Journal    
DOI: 10.1016/j.biopsych.2015.11.012     Document Type: Article

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