about
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depressionCognitive endophenotypes in a family with bipolar disorder with a risk locus on chromosome 4.GRIK4/KA1 protein expression in human brain and correlation with bipolar disorder risk variant status.A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing.A kainate receptor GluK4 deletion, protective against bipolar disorder, is associated with enhanced cognitive performance across diagnoses in the TwinsUK cohort.Vitamin intake is associated with improved visuospatial and verbal semantic memory in middle-aged individuals.Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.Interaction of nutrition and genetics via DNMT3L-mediated DNA methylation determines cognitive decline
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Q35014891-DC23C4B0-1314-4317-9081-ADFB85B5DBAFQ38457576-8E580E52-2513-4E7B-9088-B176BF083560Q39448242-6A56FEA8-A1D3-4085-A53A-C39476B31613Q45901178-4B55D8FA-21EE-4382-961E-E7B71706819EQ47564111-14A60D60-590F-49BD-A1CC-476ECE6B08FFQ47664313-1ADB7658-3FE8-4DCD-9E22-5108EAA91828Q50452939-1A3B0400-580B-4A67-88BF-6B915127388DQ92407309-FD7EAD0F-92FB-4B02-A1BD-254C2EAE5321
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Helen M Knight
@ast
Helen M Knight
@en
Helen M Knight
@es
Helen M Knight
@nl
type
label
Helen M Knight
@ast
Helen M Knight
@en
Helen M Knight
@es
Helen M Knight
@nl
prefLabel
Helen M Knight
@ast
Helen M Knight
@en
Helen M Knight
@es
Helen M Knight
@nl
P106
P31
P3762
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0000-0003-3267-9591