Helenius J Schelhaas

Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C

Andrea Olschewski, Zoltán Bálint, Eleonore Fröhlich, 2009, Nature Genetics.

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

Frank Baas, Cisca Wijmenga, Lude Franke, 2008, Nature Genetics.

Evidence for an oligogenic basis of amyotrophic lateral sclerosis.

Leonard H van den Berg, P. D. de Bakker, L. H. van den Berg, 2012, Human molecular genetics.

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.

Monitoring disease progression using high‐density motor unit number estimation in amyotrophic lateral sclerosis

Dick F Stegeman, Machiel J Zwarts, D. Stegeman, 2010, Muscle & nerve.