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A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseA polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease riskRecurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationSevere myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutationIs the saitohin gene involved in neurodegenerative diseases?PRODH mutations and hyperprolinemia in a subset of schizophrenic patientsA non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's diseaseAPP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathyEarly neurological phenotype in 4 children with biallelic PRODH mutationsGenome-wide association analysis identifies 13 new risk loci for schizophreniaABCA2 is a strong genetic risk factor for early-onset Alzheimer's diseaseMosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer DiseaseA study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease.The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.Is the urea cycle involved in Alzheimer's disease?Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
P50
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P50
description
onderzoeker
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name
Dominique Campion
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Dominique Campion
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Dominique Campion
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Dominique Campion
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type
label
Dominique Campion
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Dominique Campion
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Dominique Campion
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Dominique Campion
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prefLabel
Dominique Campion
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Dominique Campion
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Dominique Campion
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Dominique Campion
@sl