about
Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous geneAn inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.Synaptic scaffold evolution generated components of vertebrate cognitive complexity.DISC1 in schizophrenia: genetic mouse models and human genomic imaging.Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.Genetics of schizophrenia.Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.Phosphorylation of microtubule-associated protein IB and axonal growth.A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia.Using mouse transgenic and human stem cell technologies to model genetic mutations associated with schizophrenia and autism.Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder.Stem Cells to Inform the Neurobiology of Mental IllnessAssociation of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK BiobankDISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illnessAssociation of whole-genome and NETRIN1 signaling pathway-derived polygenic risk scores for Major Depressive Disorder and thalamic radiation white matter microstructure in UK BiobankReversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imagingHippoCA3mpal Stem Cell Models Expose Dysfunctional Circuits in SchizophreniaFamilial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mandy Johnstone
@ast
Mandy Johnstone
@en
Mandy Johnstone
@es
Mandy Johnstone
@nl
type
label
Mandy Johnstone
@ast
Mandy Johnstone
@en
Mandy Johnstone
@es
Mandy Johnstone
@nl
prefLabel
Mandy Johnstone
@ast
Mandy Johnstone
@en
Mandy Johnstone
@es
Mandy Johnstone
@nl
P106
P31
P496
0000-0002-8398-0862