about
Altered serotonergic function may partially account for behavioral endophenotypes in steroid sulfatase-deficient mice.The Role of the Y Chromosome in Brain Function.Understanding the pathophysiology of postpartum psychosis: Challenges and new approaches.Genetic and pharmacological modulation of the steroid sulfatase axis improves response control; comparison with drugs used in ADHD.Imprinted gene expression in the brain.Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice.X-linked imprinting: effects on brain and behaviour.Genomic imprinting effects on brain development and function.Dissociable effects of Sry and sex chromosome complement on activity, feeding and anxiety-related behaviours in miceGenomic imprinting and the social brain.Steroid sulfatase-deficient mice exhibit endophenotypes relevant to attention deficit hyperactivity disorder.The influence of sex-linked genetic mechanisms on attention and impulsivity.Functional themes from psychiatric genome-wide screens.Behavioural and Psychiatric Phenotypes in Men and Boys with X-Linked Ichthyosis: Evidence from a Worldwide Online SurveyIt is not all hormones: alternative explanations for sexual differentiation of the brain.The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders.Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder.What are imprinted genes doing in the brain?Converging pharmacological and genetic evidence indicates a role for steroid sulfatase in attention.A pharmacological mouse model suggests a novel risk pathway for postpartum psychosis.Altered brain gene expression but not steroid biochemistry in a genetic mouse model of neurodevelopmental disorder.The role of imprinted genes in mediating susceptibility to neuropsychiatric disorders.Genomic imprinting on the X chromosome: implications for brain and behavioral phenotypes.Using mouse models to investigate sex-linked genetic effects on brain, behaviour and vulnerability to neuropsychiatric disorders.Sex differences in attention Deficit Hyperactivity Disorder: candidate genetic and endocrine mechanisms.Attention deficit hyperactivity disorder (ADHD) in phenotypically similar neurogenetic conditions: Turner syndrome and the RASopathiesFamilial digit ratio (2D:4D) associations in a general population sample from Wales.X-linked ichthyosis associated with psychosis and behavioral abnormalities: a case reportInsights into rare diseases from social media surveys.Effects on fear reactivity in XO mice are due to haploinsufficiency of a non-PAR X gene: implications for emotional function in Turner's syndrome.Preliminary Evidence for Aortopathy and an X-Linked Parent-of-Origin Effect on Aortic Valve Malformation in a Mouse Model of Turner Syndrome.The steroid sulfate axis and its relationship to maternal behavior and mental health.X-monosomy effects on visuospatial attention in mice: a candidate gene and implications for Turner syndrome and attention deficit hyperactivity disorder.Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain.Do Defective Immune System-Mediated Myelination Processes Increase Postpartum Psychosis Risk?Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosisVisuospatial attentional functioning in mice: interactions between cholinergic manipulations and genotypeDoes steroid sulfatase deficiency influence postpartum psychosis risk?Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK BiobankAn Analysis of Cellular Communication Network Factor Proteins as Candidate Mediators of Postpartum Psychosis Risk
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description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
@hy
name
William Davies
@ast
William Davies
@en
William Davies
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William Davies
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William Davies
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type
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William Davies
@ast
William Davies
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William Davies
@es
William Davies
@nl
William Davies
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prefLabel
William Davies
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William Davies
@en
William Davies
@es
William Davies
@nl
William Davies
@sl
P106
P21
P31
P496
0000-0002-7714-2440