LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domain

Parlar, S. C., Senkevich, K., Yu, E., Ruskey, J. A., Ahmad, J., Asayesh, F., Spiegelman, D., Waters, C., Monchi, O., Dauvilliers, Y., Dupré, N., Greenbaum, L., Hassin-Baer, S., Miliukhina, I., Timofeeva, A., Emelyanov, A., Pchelina, S., Alcalay, R. N., Fon, E. A., … Gan-Or, Z. (2025). LRRK2 rare-variant per-domain genetic burden in Parkinson’s Disease: association confined to the kinase domain. Npj Parkinson’s Disease, 11(1). https://doi.org/10.1038/s41531-025-00934-z
Authors:
Sitki Cem Parlar
Konstantin Senkevich
Eric Yu
Jennifer A Ruskey
Jamil Ahmad
Farnaz Asayesh
Dan Spiegelman
Cheryl Waters
Oury Monchi
Yves Dauvilliers
Nicolas Dupré
Lior Greenbaum
Sharon Hassin-Baer
Irina Miliukhina
Alla Timofeeva
Anton Emelyanov
Sofya Pchelina
Roy N Alcalay
Edward A Fon
Jean-François Trempe
Ziv Gan-Or
Affiliated Authors:
Cheryl Waters
Roy N Alcalay
Publication Type:
Article
Unique ID:
10.1038/s41531-025-00934-z
PMID:
Publication Date:
Data Source:
PubMed

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