about
Novel genetic loci underlying human intracranial volume identified through genome-wide associationCommon genetic variants influence human subcortical brain structuresNovel genetic loci associated with hippocampal volume.Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia.Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia.Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 SubphenotypesA Longitudinal Model of Human Neuronal Differentiation for Functional Investigation of Schizophrenia Polygenic RiskThe Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and PlasmaWhole blood transcriptome analysis in bipolar disorder reveals strong lithium effectContribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolatesThe genetic architecture of the human cerebral cortexGenetic architecture of subcortical brain structures in 38,851 individualsComplement genes contribute sex-biased vulnerability in diverse disorders
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P50
description
researcher ORCID ID = 0000-0002-3327-7837
@en
wetenschapper
@nl
name
Loes M Olde Loohuis
@ast
Loes M Olde Loohuis
@en
Loes M Olde Loohuis
@nl
type
label
Loes M Olde Loohuis
@ast
Loes M Olde Loohuis
@en
Loes M Olde Loohuis
@nl
prefLabel
Loes M Olde Loohuis
@ast
Loes M Olde Loohuis
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Loes M Olde Loohuis
@nl
P31
P496
0000-0002-3327-7837