P. V. Doormaal

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Ewout J N Groen, Machiel J Zwarts, Fernando Rivadeneira, 2009, Nature Genetics.

Effect of Presymptomatic BodyMass Index and Consumption of Fat and Alcohol on Amyotrophic Lateral Sclerosis

J. Veldink, H. J. Schelhaas, J. Vries, 2015 .

Prior medical conditions and the risk of amyotrophic lateral sclerosis

J. Veldink, A. Visser, N. Voermans, 2014, Journal of Neurology.

Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers

Annelot M. Dekker, M. V. van Es, J. Veldink, 2016, Neurobiology of Aging.

CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis

Ewout J. N. Groen, F. Diekstra, L. H. van den Berg, 2012, Neurobiology of Aging.

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study

Ewout J. N. Groen, D. Rujescu, S. Corti, 2014, Neurobiology of Aging.

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis

A. Al-Chalabi, C. Shaw, P. Andersen, 2013, Neurobiology of Aging.

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

Naomi R. Wray, Mamede de Carvalho, Blaz Koritnik, 2018, bioRxiv.