AVPR1a and SLC6A4 gene polymorphisms are associated with creative dance performance.The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysisMeta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorderGenome-wide association scan of the time to onset of attention deficit hyperactivity disorderIndividual differences in allocation of funds in the dictator game associated with length of the arginine vasopressin 1a receptor RS3 promoter region and correlation between RS3 length and hippocampal mRNAD-serine efficacy as add-on pharmacotherapy to risperidone and olanzapine for treatment-refractory schizophreniaAHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophreniaGenome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorderMolecular genetic studies of the arginine vasopressin 1a receptor (AVPR1a) and the oxytocin receptor (OXTR) in human behaviour: from autism to altruism with some notes in betweenGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsAssociation between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skillsEffect of lithium on the physostigmine-induced behavioral syndrome and plasma cyclic GMPHaplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotypeU-shaped relation between plasma oxytocin levels and behavior in the trust gameGenetic variation in CD38 and breastfeeding experience interact to impact infants' attention to social eye cues.Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scanConduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics studyGenome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associationsEffects of arginine vasopressin on musical working memory.Genetics of human social behavior.The contributions of oxytocin and vasopressin pathway genes to human behavior.The oxytocin receptor (OXTR) contributes to prosocial fund allocations in the dictator game and the social value orientations task.Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the Psychomotor Vigilance Test.Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program.Monoamine oxidase A gene (MAOA) associated with attitude towards longshot risksGenome-wide association scan of attention deficit hyperactivity disorderDopamine D4 receptor gene associated with fairness preference in ultimatum gameDissociable contribution of prefrontal and striatal dopaminergic genes to learning in economic games.The impact of study design and diagnostic approach in a large multi-centre ADHD study. Part 1: ADHD symptom patternsThe impact of study design and diagnostic approach in a large multi-centre ADHD study: Part 2: Dimensional measures of psychopathology and intelligence.Differential genetic susceptibility to child risk at birth in predicting observed maternal behavior.Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypesMeta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorderEffect of bipolar disorder on lymphocyte inositol monophosphatase mRNA levels.A haplotype relative risk study of the dopamine D4 receptor (DRD4) exon III repeat polymorphism and attention deficit hyperactivity disorder (ADHD).Oxytonergic circuitry sustains and enables creative cognition in humans.Human maternal behaviour is associated with arginine vasopressin receptor 1A gene.AVPR1A variant associated with preschoolers' lower altruistic behavior.Copy number variation of the SELENBP1 gene in schizophreniaIdentifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.
P50
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P50
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Richard Ebstein
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Richard P. Ebstein
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Richard P. Ebstein
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type
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Richard Ebstein
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Richard P Ebstein
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R P Ebstein
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Richard Ebstein
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Richard P Ebstein
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Richard P Ebstein
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Richard P. Ebstein
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Richard P. Ebstein
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P1006
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