Pages that link to "Q45176969"

The following pages link to Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study (Q45176969):

Displayed 50 items.

• Multifinality in the development of personality disorders: a Biology x Sex x Environment interaction model of antisocial and borderline traits (Q24649658) ‎ (← links)
• Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder (Q24652360) ‎ (← links)
• Affect-modulated startle: interactive influence of catechol-O-methyltransferase Val158Met genotype and childhood trauma (Q28728111) ‎ (← links)
• Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort (Q28744011) ‎ (← links)
• Meta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity (Q30277686) ‎ (← links)
• Depression and anxiety in relation to catechol-O-methyltransferase Val158Met genotype in the general population: the Nord-Trøndelag Health Study (HUNT). (Q33346638) ‎ (← links)
• Poor replication of candidate genes for major depressive disorder using genome-wide association data (Q33547331) ‎ (← links)
• COMT Val158Met, but not BDNF Val66Met, is associated with white matter abnormalities of the temporal lobe in patients with first-episode, treatment-naïve major depressive disorder: a diffusion tensor imaging study (Q33838797) ‎ (← links)
• Modification of depression by COMT val158met polymorphism in children exposed to early severe psychosocial deprivation (Q33938160) ‎ (← links)
• Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women (Q34016279) ‎ (← links)
• Interaction of chronic stress with serotonin transporter and catechol-O-methyltransferase polymorphisms in predicting youth depression (Q34054130) ‎ (← links)
• The impact of the Val158Met catechol-O-methyltransferase genotype on neural correlates of sad facial affect processing in patients with bipolar disorder and their relatives (Q34128418) ‎ (← links)
• The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons (Q34498146) ‎ (← links)
• The catechol-O-methyl transferase Val158Met polymorphism and experience of reward in the flow of daily life (Q34661215) ‎ (← links)
• Meta-analyses of genetic studies on major depressive disorder (Q34701323) ‎ (← links)
• The effects of gender and COMT Val158Met polymorphism on fearful facial affect recognition: a fMRI study (Q34829033) ‎ (← links)
• Early institutionalization: neurobiological consequences and genetic modifiers. (Q34999520) ‎ (← links)
• A neurogenetics approach to defining differential susceptibility to institutional care (Q35049949) ‎ (← links)
• COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study (Q35202841) ‎ (← links)
• A novel SNP in COMT is associated with alcohol dependence but not opiate or nicotine dependence: a case control study (Q35712064) ‎ (← links)
• Genetic Variation in the Catechol-O-Methyl Transferase Val108/158Met Is Linked to the Caudate and Posterior Cingulate Cortex Volume in Healthy Subjects: Voxel-Based Morphometry Analysis of Brain Magnetic Resonance Imaging (Q35840931) ‎ (← links)
• Genetic biomarkers of depression (Q36064163) ‎ (← links)
• Genetic tests of biologic systems in affective disorders. (Q36154264) ‎ (← links)
• Psychiatric outcomes in young children with a history of institutionalization (Q36241848) ‎ (← links)
• Major affective disorders and schizophrenia: a common molecular signature? (Q36569474) ‎ (← links)
• Molecular genetics of bipolar disorder and depression. (Q36713347) ‎ (← links)
• Molecular studies of major depressive disorder: the epigenetic perspective (Q36786517) ‎ (← links)
• Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes (Q37003743) ‎ (← links)
• Investigating the molecular basis of major depressive disorder etiology: a functional convergent genetic approach (Q37039341) ‎ (← links)
• Genetic and environmental factors in complex neurodevelopmental disorders (Q37108117) ‎ (← links)
• Incomplete coverage of candidate genes: a poorly considered bias (Q37108126) ‎ (← links)
• Molecular epidemiology of major depressive disorder (Q37198752) ‎ (← links)
• The COMT Val158Met polymorphism and cognition in depressed and nondepressed older adults (Q37222256) ‎ (← links)
• Epigenetics and Neural developmental disorders: Washington DC, September 18 and 19, 2006 (Q37238104) ‎ (← links)
• Association analysis of the COMT/MTHFR genes and geriatric depression: an MRI study of the putamen (Q37265182) ‎ (← links)
• Emotional symptoms in children: The effect of maternal depression, life events, and COMT genotype (Q37351544) ‎ (← links)
• Reduced brain activation during inhibitory control in children with COMT Val/Val genotype (Q37514479) ‎ (← links)
• Catechol-O-methyltransferase gene val158met polymorphism and depressive symptoms during early childhood (Q37620054) ‎ (← links)
• Advances in molecular genetics of panic disorder (Q37667843) ‎ (← links)
• Children at risk for depression: memory biases, self-schemas, and genotypic variation (Q37724184) ‎ (← links)
• Genetics of depression: an overview of the current science (Q37847575) ‎ (← links)
• Genetic and neurocognitive foundations of emotion abnormalities in bipolar disorder (Q38054178) ‎ (← links)
• Associations of endocrine stress-related gene polymorphisms with risk of autism spectrum disorders: Evidence from an integrated meta-analysis (Q38705661) ‎ (← links)
• Identifying genes in monoamine nuclei that may determine stress vulnerability and depressive behavior in Wistar-Kyoto rats (Q39543910) ‎ (← links)
• Catechol-O-methyltransferase Val158Met genotype and the clinical responses to duloxetine treatment or plasma levels of 3-methoxy-4-hydroxyphenylglycol and homovanillic acid in Japanese patients with major depressive disorder (Q39625250) ‎ (← links)
• Dopaminergic Genetic Polymorphisms Predict Rule-based Category Learning (Q41226794) ‎ (← links)
• Association between COMT Val158Met and DAT1 polymorphisms and depressive symptoms in the obese population. (Q41522675) ‎ (← links)
• The COMT gene variant is associated with depression's decreased positive affect symptoms in Chinese adults. (Q41952905) ‎ (← links)
• Enhancing outcomes from major depression: using antidepressant combination therapies with multifunctional pharmacologic mechanisms from the initiation of treatment. (Q44412610) ‎ (← links)
• Catechol-O-methyltransferase Val158 Met genotype, parenting practices and adolescent alcohol use: testing the differential susceptibility hypothesis (Q45405623) ‎ (← links)