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Human Molecular Genetics|August 6, 2010
A large genome scan for rare CNVs in amyotrophic lateral sclerosisHylke M Blauw, Ammar Al-Chalabi, Peter M Andersen, et al.Annals of Neurology|December 23, 2011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosisMichael A van Es, Helenius J Schelhaas, Paul W J van Vught, et al.Nature Genetics|September 8, 2009
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosisMichael A van Es, Jan H Veldink, Christiaan G J Saris, et al.Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.Pageof 6