Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson diseaseAlexandria Beilina, Sean Chong, Suneil K. Kalia et al.|Proceedings of the National Academy of Sciences|2014Cited by 367
Genome sequence analyses identify novel risk loci for multiple system atrophyRuth Chia|Neuron|2024Cited by 41
Genome‐Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J. Billingsley, Andrew Singleton, Jinhui Ding et al.|Annals of Neurology|2023Cited by 37