about
Rare chromosomal deletions and duplications increase risk of schizophreniaA 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardationSpeeding disease gene discovery by sequence based candidate prioritizationCandidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18The NPAS3 gene--emerging evidence for a role in psychiatric illnessConfirmed rare copy number variants implicate novel genes in schizophreniaDISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signalingGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsSerine proteases in rodent hippocampus.A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depressionChromosomal abnormalities and mental illness.Genetics of schizophrenia and bipolar affective disorder: strategies to identify candidate genes.Cytogenetics and gene discovery in psychiatric disorders.Metabolomic Profiling of Post-Mortem Brain Reveals Changes in Amino Acid and Glucose Metabolism in Mental Illness Compared with ControlsCopy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness.Disrupted-in-Schizophrenia-1.Progress in defining the biological causes of schizophrenia.Schizophrenia biomarkers: translating the descriptive into the diagnostic.Enhanced gene expression in the brain following intravenous administration of lactoferrin-bearing polypropylenimine dendriplex.The EpiTect Methyl qPCR Assay as novel age estimation method in forensic biology.Specialized Information Processing Deficits and Distinct Metabolomic Profiles Following TM-Domain Disruption of Nrg1.A gene trap mutagenesis screen for genes underlying cellular response to the mood stabilizer lithium.Genomics of Lithium Action and Response.GRIK4/KA1 protein expression in human brain and correlation with bipolar disorder risk variant status.Transcriptional regulation of neurodevelopmental and metabolic pathways by NPAS3.A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.A GRIK4 variant conferring protection against bipolar disorder modulates hippocampal function.Modulation of hippocampal activation by genetic variation in the GRIK4 gene.Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?SUSPECTS: enabling fast and effective prioritization of positional candidatesAssociation of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish populationAre some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1.Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in development.The PDE4B gene confers sex-specific protection against schizophrenia.Cytogenetic and genetic evidence supports a role for the kainate-type glutamate receptor gene, GRIK4, in schizophrenia and bipolar disorder.Imprinting mechanisms.Unbalanced whole arm translocation resulting in loss of 18p in dystonia.Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder.
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Benjamin S Pickard
@ast
Benjamin S Pickard
@en
Benjamin S Pickard
@es
Benjamin S Pickard
@nl
Benjamin S Pickard
@sl
type
label
Benjamin S Pickard
@ast
Benjamin S Pickard
@en
Benjamin S Pickard
@es
Benjamin S Pickard
@nl
Benjamin S Pickard
@sl
altLabel
Ben Pickard
@en
Benjamin Pickard
@en
prefLabel
Benjamin S Pickard
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Benjamin S Pickard
@en
Benjamin S Pickard
@es
Benjamin S Pickard
@nl
Benjamin S Pickard
@sl
P1053
K-3923-2014
P106
P1153
8966860200
P21
P31
P3829
P496
0000-0002-2374-6329