Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission

Molecular Psychiatry

Volumn 12, Issue 4, 2007, Pages 367-375

  Mulle, J G ^a   Fallin, M D ^b   Lasseter, V K ^a   McGrath, J A ^a   Wolyniec, P S ^a   Pulver, A E ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

18p11; Bipolar disorder; Genetic association; Parent of origin; Psychiatric genetics; Transmission disequilibrium

Indexed keywords

ADULT; ARTICLE; BIPOLAR I DISORDER; CHROMOSOME 18P; CONTROLLED STUDY; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; HYPOTHESIS; JEW; MAJOR CLINICAL STUDY; MALE; PATERNITY; PEDIGREE ANALYSIS; PHENOTYPE; POPULATION GENETICS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; BIPOLAR DISORDER; CHROMOSOMES, HUMAN, PAIR 18; FAMILY HEALTH; FATHER-CHILD RELATIONS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; JEWS; LINKAGE DISEQUILIBRIUM; LONGITUDINAL STUDIES; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33947625116     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/sj.mp.4001916     Document Type: Article

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