Maternal depression and child and adolescent depression symptoms: An exploratory test for moderation by CRHR1, FKBP5 and NR3C1 gene variants

Behavior Genetics

Volumn 42, Issue 1, 2012, Pages 121-132

  Lewis, Gemma ^a   Collishaw, Stephan ^a   Harold, Gordon ^c   Rice, Frances ^b   Thapar, Anita ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY OF LEICESTER   (United Kingdom)

Author keywords

Child and adolescent depression; Gene environment interaction; Maternal depression; Single nucleotide polymorphism

Indexed keywords

ADOLESCENT; ADULT; AGE DISTRIBUTION; ARTICLE; CHILD; CONTROLLED STUDY; CRHR1 GENE; FEMALE; FKBP5 GENE; GENE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MAJOR DEPRESSION; MALE; MATERNAL DISEASE; NR3C1 GENE; POPULATION RESEARCH; PROGENY; RECURRENT DISEASE; REGISTER; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SYMPTOMATOLOGY;

ADOLESCENT; ADULT; CHILD; DEPRESSION; FEMALE; GENETIC VARIATION; GENOTYPE; HUMANS; MALE; MODELS, GENETIC; MODELS, THEORETICAL; MOTHERS; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, CORTICOTROPIN-RELEASING HORMONE; RECEPTORS, GLUCOCORTICOID; RISK; TACROLIMUS BINDING PROTEINS;

EID: 84856670875     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-011-9482-1     Document Type: Article

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