Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Ammar Al‐Chalabi, Cathryn M. Lewis et al.|The Lancet Neurology|2010Cited by 226
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosisMichael A. van Es, Roel A. Ophoff, Helenius J. Schelhaas et al.|Annals of Neurology|2011Cited by 203
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European originsShai Carmi, Itsik Pe’er, Ken Hui et al.|Nature Communications|2014Cited by 197
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis RiskMitja Mitrovič, Nadia Barizzone, Nikolaos A. Patsopoulos et al.|Cell|2018Cited by 172
Diagnostic and Prognostic Performance of Neurofilaments in ALSKoen Poesen, Philip Van Damme|Frontiers in Neurology|2019Cited by 138