Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteriaGünter U. Höglinger, Gesine Respondek, María Stamelou et al.|Movement Disorders|2017Cited by 2.3k
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathwaysElizabeth T. Cirulli, Wendy K. Chung, Brittany N. Lasseigne et al.|Science|2015Cited by 980
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M. Van Deerlin, Howard Feldman, Stuart Pickering‐Brown et al.|Nature Genetics|2010Cited by 608
Which ante mortem clinical features predict progressive supranuclear palsy pathology?Gesine Respondek, Carolin Kurz, Thomas Arzberger et al.|Movement Disorders|2017Cited by 163
Preventing amyotrophic lateral sclerosis: insights from pre-symptomatic neurodegenerative diseasesMichael Benatar, Joanne Wuu, Caroline McHutchison et al.|Brain|2021Cited by 116