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(21 - 37 of 37)

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Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
A promoter-level mammalian expression atlas
An atlas of active enhancers across human cell types and tissues
Genetic comorbidities in Parkinson's disease
Cervical dystonia and genetic common variation in the dopamine pathway
Dissecting the genetic make-up of North-East Sardinia using a large set of haploid and autosomal markers
A Fine-Mapping Study of 7 Top Scoring Genes from a GWAS for Major Depressive Disorder
Catechol-O-methyltransferase Val158Met and the Risk of Dyskinesias in Parkinson's Disease
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Genome-wide association study confirms extant PD risk loci among the Dutch
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
Melanocortin-4 Receptor Gene Mutations in a Dutch Cohort of Obese Children
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Analysis of variation in the melanocortin-4 receptor gene (mc4r) in golden retriever dogs
Investigation of a Patient With a Partial Trisomy 16q Including the Fat Mass and Obesity Associated Gene (FTO): Fine Mapping and FTO Gene Expression Study

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