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Traffic (Copenhagen, Denmark)|October 25, 2013
The Vps35 D620N mutation linked to Parkinson's disease disrupts the cargo sorting function of retromerJordan Follett, Suzanne J Norwood, Nicholas A Hamilton, et al.
Brain Research|June 16, 2025
Regulation of LRRK2 activity by metabolic stress and heavy metal exposureMichalis Kentros, Jordan Follett, Nitya Subrahmanian, et al.
Annals of Neurology|September 12, 2017
DNAJC12 and dopa-responsive nonprogressive parkinsonismLetizia Straniero, Ilaria Guella, Roberto Cilia, et al.
Plos Genetics|June 7, 2019
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of diseaseCarles Vilariño-Güell, Alexander Zimprich, Filippo Martinelli-Boneschi, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Brain : a Journal of Neurology|April 16, 2025
Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophyViorica Chelban, David Pellerin, Nirosen Vijiaratnam, et al.
Annals of Neurology|May 3, 2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's DiseaseDongbing Lai, Babak Alipanahi, Pierre Fontanillas, et al.
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