Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach.
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Toward an integration of cognitive and genetic models of risk for depressionFKBP51 and FKBP52 in signaling and diseaseFKBP5 moderates alcohol withdrawal severity: human genetic association and functional validation in knockout mice.A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder.The common functional FKBP5 variant rs1360780 is associated with altered cognitive function in aged individualsPersonalized medicine in psychiatry: problems and promises.Systematic review of genome-wide gene expression studies of bipolar disorderStress-related genes and heroin addiction: a role for a functional FKBP5 haplotypeInvestigation of genetic variants, birthweight and hypothalamic-pituitary-adrenal axis function suggests a genetic variant in the SERPINA6 gene is associated with corticosteroid binding globulin in the western Australia pregnancy cohort (Raine) studThe Rotterdam Study: 2012 objectives and design update.Polymorphism in COMT is associated with IgG3 subclass level and susceptibility to infection in patients with chronic fatigue syndrome.The Rotterdam Study: 2016 objectives and design update.Elucidating molecular networks that either affect or respond to plasma cortisol concentration in target tissues of liver and muscleGenetic association of FKBP5 and CRHR1 with cortisol response to acute psychosocial stress in healthy adults.GLUCOCORTICOID RECEPTOR-RELATED GENES: GENOTYPE AND BRAIN GENE EXPRESSION RELATIONSHIPS TO SUICIDE AND MAJOR DEPRESSIVE DISORDERThe role of limbic system irritability in linking history of childhood maltreatment and psychiatric outcomes in low-income, high-risk women: moderation by FK506 binding protein 5 haplotypeMetyrapone in treatment-resistant depression.FKBP5 genetic variation: association with selective serotonin reuptake inhibitor treatment outcomes in major depressive disorder.FKBP5 and emotional neglect interact to predict individual differences in amygdala reactivity.Possible association between haplotypes of the FKBP5 gene and suicidal bipolar disorder, but not with melancholic depression and psychotic features, in the course of bipolar disorder.Association of FKBP5 polymorphisms and resting-state activity in a frontotemporal-parietal network.A neurogenetics approach to understanding individual differences in brain, behavior, and risk for psychopathology.Gene-environment interactions at the FKBP5 locus: sensitive periods, mechanisms and pleiotropism.Depression and antidepressant use moderate association between widowhood and Alzheimer's disease.The genetics of loneliness: linking evolutionary theory to genome-wide genetics, epigenetics, and social science.The genetics of anxiety-related negative valence system traits.Hypothalamic-pituitary-adrenal axis genetic variation and early stress moderates amygdala function.Psychiatric symptoms in adolescents: FKBP5 genotype--early life adversity interaction effects.HPA Axis Genes, and Their Interaction with Childhood Maltreatment, are Related to Cortisol Levels and Stress-Related Phenotypes.Mood, stress and longevity: convergence on ANK3.DNA polymorphism in the FKBP5 gene affects impulsivity in intertemporal choice.The Rotterdam Study: 2014 objectives and design update.The FKBP51 Glucocorticoid Receptor Co-Chaperone: Regulation, Function, and Implications in Health and Disease.FKBP5 is associated with amygdala volume in the human brain and mood state: A voxel-based morphometry (VBM) study.FKBP5 Moderates the Association between Antenatal Maternal Depressive Symptoms and Neonatal Brain Morphology.Genetic influences on hormonal markers of chronic hypothalamic-pituitary-adrenal function in human hair.Genetic variation in FKBP5 associated with the extent of stress hormone dysregulation in major depression.The prospect of FKBP51 as a drug target.The extending spectrum of NPC1-related human disorders: from Niemann-Pick C1 Disease to obesity.Polymorphisms in the FK506 binding protein 5 gene are associated with attention deficit hyperactivity disorder and diurnal cortisol levels.
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Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 12 February 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Genetics of cortisol secretion ...... ome wide association approach.
@en
Genetics of cortisol secretion ...... ome wide association approach.
@nl
type
label
Genetics of cortisol secretion ...... ome wide association approach.
@en
Genetics of cortisol secretion ...... ome wide association approach.
@nl
prefLabel
Genetics of cortisol secretion ...... ome wide association approach.
@en
Genetics of cortisol secretion ...... ome wide association approach.
@nl
P2093
P2860
P50
P1476
Genetics of cortisol secretion ...... ome wide association approach.
@en
P2093
Andre G Uitterlinden
Brian R Walker
Cornelia M Van Duijn
Fleur P Velders
Frank C Verhulst
Marieke J Dekker
Maris Kuningas
P2860
P304
P356
10.1016/J.PSYNEUEN.2011.01.003
P577
2011-02-12T00:00:00Z