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List of works by Wouter van Rheenen

A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories

scientific article

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

scientific article

ALS in Danish Registries: Heritability and links to psychiatric and cardiovascular disorders

scientific article published on 20 February 2020

ATXN2 trinucleotide repeat length correlates with risk of ALS.

scientific article

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

scientific article published on December 2011

Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort

scientific article published on 22 September 2018

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis

scientific article published on 31 May 2016

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scientific article

Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

scientific article published on 22 December 2020

Circulating microRNAs in patients with intracranial aneurysms

scientific article

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

preprint

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scholarly article

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

scientific article published on 20 September 2017

Dutch population structure across space, time and GWAS design

scientific article published on 11 September 2020

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

scientific article published on 22 October 2014

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

scientific article published on 21 March 2017

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

scientific article published in March 2018

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

scientific article published on 25 July 2016

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

scientific article published on 16 November 2020

Genomic signals of migration and continuity in Britain before the Anglo-Saxons

scientific article published on 19 January 2016

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis

scientific article published on 11 October 2012

Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis

scientific article published on 15 May 2019

Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.

scientific article

Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

scientific article published on 26 March 2021

No association between gluten sensitivity and amyotrophic lateral sclerosis

scientific article published on 06 February 2017

Population genetic differentiation of height and body mass index across Europe

scientific article

Reconsidering the causality of TIA1 mutations in ALS.

scientific article published on 13 December 2017

Risk in Relatives, Heritability, SNP-Based Heritability, and Genetic Correlations in Psychiatric Disorders: A Review

scientific article published on 10 June 2020

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

scientific article published on 28 January 2022

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

scientific article published on 01 August 2019

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease

scientific article

Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.

scientific article published on 25 June 2018

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