Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 50, 2007, Pages 19942-19947

  Lencz, Todd ^a,b,c   Lambert, Christophe ^d   DeRosse, Pamela ^a   Burdick, Katherine E ^a,b,c   Morgan, T Vance ^e   Kane, John M ^a,b,c   Kucherlapati, Raju ^e,f   Malhotra, Anil K ^a,b,c,d  

^a ZUCKER HILLSIDE HOSPITAL   (United States)

^b FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH   (United States)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d GOLDEN HELIX INC   (United States)

^e LABORATORY FOR MOLECULAR MEDICINE   (United States)

^f HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Genomewide; Haplotype; HapMap; Selection; Susceptibility

Indexed keywords

GENOMIC DNA;

ARTICLE; CASE CONTROL STUDY; CAUCASIAN; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOME; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; PRIORITY JOURNAL; SCHIZOAFFECTIVE PSYCHOSIS; SCHIZOPHRENIA; SCHIZOPHRENIFORM DISORDER; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HOMOZYGOTE; HUMANS; MALE; PENETRANCE; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA;

EID: 38049164192     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0710021104     Document Type: Article

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