about
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaPsychosis Risk Candidate ZNF804A Localizes to Synapses and Regulates Neurite Formation and Dendritic Spine StructurePleiotropic Effects of Trait-Associated Genetic Variation on DNA Methylation: Utility for Refining GWAS Loci.Screening the human protocadherin 8 (PCDH8) gene in schizophrenia.Knockdown of the psychosis susceptibility gene ZNF804A alters expression of genes involved in cell adhesion.Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophreniaMethylomic trajectories across human fetal brain development.Effects of cis-regulatory variation differ across regions of the adult human brain.Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci.Gene expression in the etiology of schizophrenia.Transcriptional consequences of schizophrenia candidate miR-137 manipulation in human neural progenitor cells.The neurobiology of schizophrenia: new leads and avenues for treatment.Knockdown of the schizophrenia susceptibility gene TCF4 alters gene expression and proliferation of progenitor cells from the developing human neocortex.MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls.Stochastic choice of allelic expression in human neural stem cells.Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.5-hydroxymethylcytosine is highly dynamic across human fetal brain development.Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.Investigating schizophrenia in a "dish": possibilities, potential and limitations.A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain.Translating Genetic Risk Loci Into Molecular Risk Mechanisms for Schizophrenia.Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia.DISC1 mRNA expression is not influenced by common Cis-acting regulatory polymorphisms or imprinting.Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.Convergent Evidence for 2′,3′-Cyclic Nucleotide 3′-Phosphodiesterase as a Possible Susceptibility Gene for SchizophreniaAllelic expression of APOE in human brain: effects of epsilon status and promoter haplotypesThe effect of age and the H1c MAPT haplotype on MAPT expression in human brainInvestigating cis-acting regulatory variation using assays of relative allelic expressionThe high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophreniaNo evidence for allelic association between schizophrenia and a functional variant of the human dopamine ?-hydroxylase gene (DBH)Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disordersSex differences in gene expression in the human fetal brain
P50
Q24670103-A602C706-A148-4F38-96F8-815ECFC01CE4Q33288801-BAD6E751-08BC-401D-BBAA-AB801BC89693Q33807562-6B3CC007-C3F0-401A-AB37-1AEF9E6876A3Q34217651-84CF2521-6E96-415F-A303-30EAFDDEEE99Q34232304-FD612889-46E4-4D0D-8885-8CFCE8DC387CQ34676602-6F044322-4ED4-48BD-8C3A-07D35F2119A5Q35157209-92545650-4AA6-4E5E-94B3-FC4E0DE03237Q35819825-5E965974-9150-4289-85C4-D71822EFDE77Q36466426-5273B197-AF66-45AA-A0C4-975431DDAA20Q37107674-2C366945-DD8E-4C0E-9735-DFD990F5F35AQ37706529-7FE1150C-E5A4-4405-9DF6-A3204361A747Q37799057-E6B02843-6078-45B5-B7CE-9C7DC71F7638Q38442346-4F775E83-4A66-4CBD-A959-D05086440D4FQ39002120-18D8F83C-F366-4A32-A310-EC7B8D072FF1Q39328174-9CF71988-3F88-4AE3-86A8-B2B4BF591790Q40027214-C2FD3C85-C144-4F81-ABFC-CFE38C390FB0Q41704790-196D7133-22A8-405C-9213-FA7052385C87Q41713353-98352C3C-CFC2-4687-BBE3-FEDD3C811F34Q42326811-605B33CC-09DD-485A-8A00-154655FE37F2Q42928107-1A3620B2-EA2F-4B37-B3D3-ACBE27C8BB02Q43004869-8D1A43D4-FAF4-4CB7-8DE5-1B8D68255BBBQ46531741-C6FFAE83-EE7B-4773-B62D-2DDE01D9B659Q46775363-AFE5F6D4-8ADE-4D65-97EA-FE3EE3C14FEAQ51893915-C23057FB-4144-4FFE-90F6-111559E0292CQ53621277-31FC8C4B-1826-400E-8D42-253551F51886Q57279160-C6196906-8175-469D-B082-7F08501FD30CQ57279167-CB30CEC7-1C7B-40E4-9680-C0023C4AF72AQ57727210-9C356EE8-C66E-42DC-888C-F7BAA86E254CQ57727217-E751108F-16D2-459E-9BF0-00B9CF5AD4A3Q57727237-E52E3389-599B-45AC-890D-24A46AFECDEEQ57727239-60B7370A-0DAB-48AE-B935-1BCEC4E79EEAQ59129918-A5FF4C59-4676-4B33-9DEB-AB2913BD4680Q60627851-A3969679-AB73-452F-8314-8CC8A7A14649
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nicholas Bray
@ast
Nicholas Bray
@en
Nicholas Bray
@es
Nicholas Bray
@nl
type
label
Nicholas Bray
@ast
Nicholas Bray
@en
Nicholas Bray
@es
Nicholas Bray
@nl
prefLabel
Nicholas Bray
@ast
Nicholas Bray
@en
Nicholas Bray
@es
Nicholas Bray
@nl
P106
P1153
7003409020
P21
P31
P496
0000-0002-4357-574X