Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteriaGünter U. Höglinger, Dennis W. Dickson, Richard Dodel et al.|Movement Disorders|2017Cited by 2.3k
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s diseaseLaurie Robak, Karin D. van Dijk, Iris E. Jansen et al.|Brain|2017Cited by 452
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson diseaseAlexandria Beilina, Sean Chong, Iakov N. Rudenko et al.|Proceedings of the National Academy of Sciences|2014Cited by 367
A genome-wide association study in multiple system atrophyAnna Sailer, Pietro Cortelli, Sonja W. Scholz et al.|Neurology|2016Cited by 163
Which ante mortem clinical features predict progressive supranuclear palsy pathology?Gesine Respondek, Carolin Kurz, Thomas Arzberger et al.|Movement Disorders|2017Cited by 163