Richard W. Orrell

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Alan E. Renton, Elisa Majounie, Adrian J. Waite et al. · Neuron · 2011 · 4.5K citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

Elisa Majounie, Alan E. Renton, Kin Y. Mok et al. · The Lancet Neurology · 2012 · 1.2K citations · Full text

Life Sciences, Molecular Genetics, Neurology +15

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

Wouter van Rheenen, Aleksey Shatunov, Annelot M. Dekker et al. · Nature Genetics · 2016 · 628 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Neurofilament light chain

Ching‐Hua Lu, Corrie Macdonald‐Wallis, Elizabeth Gray et al. · Neurology · 2015 · 551 citations · Full text

Life Sciences, Neurology, Neuroscience +14

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Janel O. Johnson, Erik P. Pioro, Ashley Boehringer et al. · Nature Neuroscience · 2014 · 443 citations · Full text

Life Sciences, Genetics, Neuroscience +12