Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 159 B, Issue 5, 2012, Pages 549-559

  Hunter, Jessica Ezzell ^a   Leslie, Mary ^a   Novak, Gloria ^a   Hamilton, Debra ^a   Shubeck, Lisa ^a   Charen, Krista ^a   Abramowitz, Ann ^b   Epstein, Michael P ^a   Lori, Adriana ^a   Binder, Elisabeth ^a   Cubells, Joseph F ^a   Sherman, Stephanie L ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMORY UNIVERSITY   (United States)

Author keywords

Cortisol; FMR1 premutation; Fragile X syndrome; Gene environment interaction; Hypothalamic pituitary adrenal axis

Indexed keywords

HYDROCORTISONE;

ADULT; ALLELE; ANXIETY DISORDER; ARTICLE; CENTER FOR EPIDEMIOLOGIC STUDIES DEPRESSION SCALE; CORTICOTROPHIN RELEASING HORMONE RECEPTOR 1 GENE; DEPRESSION; FEMALE; FRAGILE X SYNDROME; GENE; GENE LOCUS; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HEREDITY; HUMAN; POSITIVE AND NEGATIVE AFFECT SCHEDULE; PRIORITY JOURNAL; PSYCHOLOGIC TEST; QUESTIONNAIRE; SELF REPORT; SINGLE NUCLEOTIDE POLYMORPHISM; SOCIAL PHOBIA AND ANXIETY INVENTORY; STATE TRAIT ANXIETY INVENTORY; STRESS;

ADOLESCENT; ADULT; ANXIETY; CHILD; CHILD REARING; DEMOGRAPHY; DEPRESSION; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; GENE FREQUENCY; HUMANS; LINEAR MODELS; LOGISTIC MODELS; MIDDLE AGED; MUTATION; PERSONALITY INVENTORY; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, CORTICOTROPIN-RELEASING HORMONE;

EID: 84861936832     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32061     Document Type: Article

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