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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureA double RING-H2 domain in RNF32, a gene expressed during sperm formationMutations in TITF-1 are associated with benign hereditary choreaMutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonismDJ-1 transcriptionally up-regulates the human tyrosine hydroxylase by inhibiting the sumoylation of pyrimidine tract-binding protein-associated splicing factorDisruption of a long-range cis-acting regulator for Shh causes preaxial polydactylyFrequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyImputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesA mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDClinical features and neuroimaging of PARK7-linked parkinsonismDisruption of the C7orf2/Lmbr1 genic region is associated with preaxial polydactyly in humans and miceLinking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's diseaseLarge-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseAssociation of the gene encoding neurogranin with schizophrenia in malesComprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathwaysNeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesLoss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagyIdentification of common variants influencing risk of the tauopathy progressive supranuclear palsy.Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projects.Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationDiagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling studyDGEclust: differential expression analysis of clustered count data.Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.Novel parkin mutations detected in patients with early-onset Parkinson's disease.Genome-wide prediction of functional gene-gene interactions inferred from patterns of genetic differentiation in mice and men.Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study.Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability.Frontotemporal dementia and its subtypes: a genome-wide association study.Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisGlobal similarity with local differences in linkage disequilibrium between the Dutch and HapMap-CEU populations.Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder.Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17.
P50
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P50
name
Peter Heutink
@ast
Peter Heutink
@en
Peter Heutink
@nl
type
label
Peter Heutink
@ast
Peter Heutink
@en
Peter Heutink
@nl
prefLabel
Peter Heutink
@ast
Peter Heutink
@en
Peter Heutink
@nl