A rare functional noncoding variant at the GWAS-Implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder

American Journal of Human Genetics

Volumn 95, Issue 6, 2014, Pages 744-753

  Duan, Jubao ^a,b   Shi, Jianxin ^c   Fiorentino, Alessia ^d   Leites, Catherine ^a   Chen, Xiangning ^e   Moy, Winton ^a   Chen, Jingchun ^e   Alexandrov, Boian S ^f,g   Usheva, Anny ^f   He, Deli ^a   Freda, Jessica ^a   O'Brien, Niamh L ^d   McQuillin, Andrew ^d   Sanders, Alan R ^a,b   Gershon, Elliot S ^b   Delisi, Lynn E ^f   Bishop, Alan R ^g   Gurling, Hugh M D ^d   Pato, Michele T ^h   Levinson, Douglas F ⁱ   Kendler, Kenneth S ^e   Pato, Carlos N ^h   Gejman, Pablo V ^a,b   more..

^a NORTHSHORE UNIVERSITY HEALTHSYSTEM   (United States)

^b UNIVERSITY OF CHICAGO   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^f HARVARD MEDICAL SCHOOL   (United States)

^g LOS ALAMOS NATIONAL LABORATORY   (United States)

^h UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

ⁱ STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; MICRORNA; MICRORNA 137; MICRORNA 2682; TRANSCRIPTION FACTOR YY1; UNCLASSIFIED DRUG; MIRN-2682 MICRORNA, HUMAN; MIRN137 MICRORNA, HUMAN;

ALLELE; ARTICLE; BIPOLAR DISORDER; CHROMATIN; CONTROLLED STUDY; DNA FLANKING REGION; DNA SEQUENCE; ENHANCER REGION; GENE EXPRESSION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; MAJOR CLINICAL STUDY; NERVE CELL DIFFERENTIATION; NEURAL STEM CELL; NEUROBLASTOMA CELL; PLURIPOTENT STEM CELL; POLYMERASE CHAIN REACTION; PROMOTER REGION; PROTEIN CONFORMATION; REPORTER GENE; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; TANDEM REPEAT; GENE EXPRESSION REGULATION; GENETIC PREDISPOSITION; GENETICS; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; RISK; TUMOR CELL LINE;

ALLELES; BASE SEQUENCE; BIPOLAR DISORDER; CELL LINE, TUMOR; GENE EXPRESSION REGULATION; GENE FREQUENCY; GENES, REPORTER; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MICRORNAS; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC; RISK; SCHIZOPHRENIA; SEQUENCE ANALYSIS, DNA;

EID: 84919674518     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2014.11.001     Document Type: Article

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