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Human Genetics|January 15, 2013
Increased paternal age and the influence on burden of genomic copy number variation in the general populationJacobine E Buizer-Voskamp, Hylke M Blauw, Marco P M Boks, et al.
Neurobiology of Aging|January 19, 2016
Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriersAnnelot M Dekker, Meinie Seelen, Perry T C van Doormaal, et al.
European Journal of Human Genetics : EJHG|March 14, 2026
Genetic basis of the circle of Willis characteristics in the healthy and intracranial aneurysm populationMark K Bakker, Phebe J Groenheide, Iris N Vos, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 2, 2016
Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosisBenjamin Gaastra, Aleksey Shatunov, Sara Pulit, et al.
Genome Biology|August 30, 2020
Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inferencePaul J Hop, René Luijk, Lucia Daxinger, et al.
The Pharmacogenomics Journal|October 19, 2019
Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure?Ruben P A van Eijk, Marinus J C Eijkemans, Stavros Nikolakopoulos, et al.
Archives of Neurology|February 10, 2010
FUS mutations in familial amyotrophic lateral sclerosis in the NetherlandsEwout J N Groen, Michael A van Es, Paul W J van Vught, et al.
Nature Communications|March 27, 2025
CREB3 gain of function variants protect against ALSSalim Megat, Christine Marques, Marina Hernán-Godoy, et al.
The Lancet. Neurology|February 19, 2013
Controversies and priorities in amyotrophic lateral sclerosisMartin R Turner, Orla Hardiman, Michael Benatar, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosisMichael A Van Es, Paul W J Van Vught, Jan H Veldink, et al.
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