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(1 - 24 of 28)

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WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Skewed X-inactivation is common in the general female population
Increased High-Density Lipoprotein Levels Associated with Age-Related Macular Degeneration Evidence from the EYE-RISK and European Eye Epidemiology Consortia
Mediterranean Diet and Incidence of Advanced Age-Related Macular Degeneration: The EYE-RISK Consortium
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly
Skewed X-inactivation is common in the general female population
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Genome-wide associations for birth weight and correlations with adult disease
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Population-specific genotype imputations using minimac or IMPUTE2
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
The impact of low-frequency and rare variants on lipid levels
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Whole-genome sequence variation, population structure and demographic history of the Dutch population

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