About: Walter J Muir

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University of Edinburgh; Western General Hospital

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rdf:type	Item
description	University of Edinburgh; Western General Hospital (en)
rdfs:label	Walter J Muir (de) Walter J Muir (en) Walter J Muir (es) Walter J Muir (fr) Walter J Muir (gl) Walter J Muir (it) Walter J Muir (nl) Walter J Muir (pt) Walter J Muir (sv) Walter J Muir (pt-br)
skos:prefLabel	Walter J Muir (de) Walter J Muir (en) Walter J Muir (es) Walter J Muir (fr) Walter J Muir (gl) Walter J Muir (it) Walter J Muir (nl) Walter J Muir (pt) Walter J Muir (sv) Walter J Muir (pt-br)
name	Walter J Muir (de) Walter J Muir (en) Walter J Muir (es) Walter J Muir (fr) Walter J Muir (gl) Walter J Muir (it) Walter J Muir (nl) Walter J Muir (pt) Walter J Muir (sv) Walter J Muir (pt-br)
instance of	wds:Q113645651-10C095C8-B94D-4950-9093-FDF0DEC17CF2
instance of	Homo sapiens
Dimensions author ID	wds:Q113645651-007351A3-4334-4B06-933E-2D22BB22BEC8 wds:Q113645651-526E41E2-7835-492B-A82D-03D0F8D8E1F9 wds:Q113645651-5C0B4366-CD7C-404A-A86D-64A816214880
Dimensions author ID	010153013057.24 01156276751.86 013373253572.70
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q113645651
is author of	Neuropsychological and P300 abnormalities in schizophrenics and their relatives. Nuts and bolts of psychiatric genetics: building on the Human Genome Project The experiences of adults with intellectual disabilities and their carers in general hospitals: a focus group study Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish population High harm avoidance and low self-directedness in euthymic young adults with recurrent, early-onset depression Auditory P300 does not differentiate borderline personality disorder from schizotypal personality disorder Auditory P300 in borderline personality disorder and schizophrenia Mutational screening and association study of glutamate decarboxylase 1 as a candidate susceptibility gene for bipolar affective disorder and schizophrenia Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family. Borderline personality disorder characteristics in young adults with recurrent mood disorders: a comparison of bipolar and unipolar depression Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder Chromosomal abnormalities and mental illness. Presence of multiple functional polyadenylation signals and a single nucleotide polymorphism in the 3' untranslated region of the human serotonin transporter gene. Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Whole-genome association study of bipolar disorder Disruption of two novel genes by a translocation co-segregating with schizophrenia Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42 A long-range restriction map across 3 Mb of the chromosome 11 breakpoint region of a translocation linked to schizophrenia: localization of the breakpoint and the search for neighbouring genes Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder. Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia. Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia. Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia Markers close to the dopamine D5 receptor gene (DRD5) show significant association with schizophrenia but not bipolar disorder GRIK4/KA1 protein expression in human brain and correlation with bipolar disorder risk variant status A GRIK4 variant conferring protection against bipolar disorder modulates hippocampal function. Cytogenetic and genetic evidence supports a role for the kainate-type glutamate receptor gene, GRIK4, in schizophrenia and bipolar disorder. DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder. The PDE4B gene confers sex-specific protection against schizophrenia. A common variant in the 3'UTR of the GRIK4 glutamate receptor gene affects transcript abundance and protects against bipolar disorder Grey matter correlates of early psychotic symptoms in adolescents at enhanced risk of psychosis: a voxel-based study. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Neurocognitive impairment in euthymic young adults with bipolar spectrum disorder and recurrent major depressive disorder Transcriptional regulation of neurodevelopmental and metabolic pathways by NPAS3. Long-latency auditory event-related potentials in schizophrenia and in bipolar and unipolar affective disorder Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo Case-control study of neurocognitive function in euthymic patients with bipolar disorder: an association with mania. Auditory P300 and eye tracking dysfunction in schizophrenic pedigrees. Support for a bipolar affective disorder susceptibility locus on chromosome 12q24.3. Confirmed rare copy number variants implicate novel genes in schizophrenia Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European multicenter association study of affective disorders Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population. Analysis and metaanalysis of two polymorphisms within the tyrosine hydroxylase gene in bipolar and unipolar affective disorders Association analyses suggestGPR24 as a shared susceptibility gene for bipolar affective disorder and schizophrenia Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder Structure of a variable number tandem repeat of the serotonin transporter gene and association with affective disorder Disruption of the neuronal PAS3 gene in a family affected with schizophrenia Disruption of a brain transcription factor, NPAS3, is associated with schizophrenia and learning disability Linkage Analysis in a Large Family from Pakistan with Depression and a High Incidence of Consanguineous Marriages The effects of cortisol infusion upon hormone secretion from the anterior pituitary and subjective mood in depressive illness and in controls Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing. A locus for bipolar affective disorder on chromosome 4p Auditory P300 event-related potentials and neuropsychological performance in schizophrenia and bipolar affective disorder SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis. Candidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18

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