Jeroen van Rooij

Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing

External Test of a Deep Learning Algorithm for Pulmonary Nodule Malignancy Risk Stratification Using European Screening Data

Lifestyle factors and metabolomic aging biomarkers: Meta-analysis of cross-sectional and longitudinal associations in three prospective cohorts

Genome-Wide Interaction Analysis With DASH Diet Score Identified Novel Loci for Systolic Blood Pressure

Multi-source data approach for personalized outcome prediction in lung cancer screening: update from the NELSON trial

Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan

Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

Novel <scp>CSF</scp> biomarkers in genetic frontotemporal dementia identified by proteomics

Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

Identification of context-dependent expression quantitative trait loci in whole blood

Quantifying prion disease penetrance using large population control cohorts

Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis

The transcriptional landscape of age in human peripheral blood

Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations