about
COMT Val158Met × SLC6A4 5-HTTLPR interaction impacts on gray matter volume of regions supporting emotion processing.Predicting outcomes following cognitive behaviour therapy in child anxiety disorders: the influence of genetic, demographic and clinical information.Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression.Therapygenetics: the 5HTTLPR and response to psychological therapy.Neurotrophic gene polymorphisms and response to psychological therapy.Ohnologs are overrepresented in pathogenic copy number mutations.Clinical utility gene card for: 16p13.11 microdeletion syndromeMicroduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions.Clinical utility gene card for: 15q13.3 microdeletion syndrome.The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression.Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014.Association analysis of STX1A gene variants in common forms of migraine.No association between bipolar disorder risk polymorphisms in ANK3 and CACNA1C and common migraine.No association between the Catechol-O-Methyltransferase (COMT) val158met polymorphism and cognitive improvement following cognitive remediation therapy (CRT) in schizophrenia
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Maria Tropeano
@ast
Maria Tropeano
@en
Maria Tropeano
@es
Maria Tropeano
@nl
Maria Tropeano
@sl
type
label
Maria Tropeano
@ast
Maria Tropeano
@en
Maria Tropeano
@es
Maria Tropeano
@nl
Maria Tropeano
@sl
prefLabel
Maria Tropeano
@ast
Maria Tropeano
@en
Maria Tropeano
@es
Maria Tropeano
@nl
Maria Tropeano
@sl
P1053
E-7611-2011
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P3829
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0000-0002-5156-7539