Matthew Farrer, PhD, Imperial College
Affiliations: | Neurogenetics and Translational Medicine | University of British Columbia, Vancouver, Vancouver, BC, Canada |
Area:
Neurodegenerative diseasesWebsite:
http://www.cmmt.ubc.ca/research/investigators/farrer/labGoogle:
"Matthew Farrer"Mean distance: 19.3 (cluster 28)
Cross-listing: Alzheimer's Tree
Children
Sign in to add trainee| Emil Karl Gustavsson | grad student | Univesity of British Columia (UBC) | |
| Igor Tatarnikov | grad student | 2015- | UBC (FlyTree) |
| Stefano Cataldi | grad student | 2014-2018 | UBC (FlyTree) |
| Bahareh Behrouz | post-doc | 2008-2010 | Mayo Clinic Jacksonville |
BETA: Related publications
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Publications
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| Gustavsson EK, Follett J, Trinh J, et al. (2024) RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses. The Lancet. Neurology |
| Gustavsson EK, Follett J, Trinh J, et al. (2024) A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and . Medrxiv : the Preprint Server For Health Sciences |
| Follett J, Guenther D, Xoi L, et al. (2024) Genetic Modifiers of LRRK2 Parkinson's Disease: A Replication Study in Arab-Berbers. Movement Disorders : Official Journal of the Movement Disorder Society |
| Bu M, Follett J, Deng I, et al. (2023) Inhibition of LRRK2 kinase activity rescues deficits in striatal dopamine physiology in VPS35 p.D620N knock-in mice. Npj Parkinson's Disease. 9: 167 |
| Kawakami F, Imai M, Isaka Y, et al. (2023) LRRK2 negatively regulates glucose tolerance via regulation of membrane translocation of GLUT4 in adipocytes. Febs Open Bio |
| Müller-Nedebock AC, Dekker MCJ, Farrer MJ, et al. (2023) Different pieces of the same puzzle: a multifaceted perspective on the complex biological basis of Parkinson's disease. Npj Parkinson's Disease. 9: 110 |
| Nakahara Y, Mitsui J, Date H, et al. (2023) Genome-wide association study identifies a new susceptibility locus in for Multiple System Atrophy. Medrxiv : the Preprint Server For Health Sciences |
| Gabbert C, Schaake S, Lüth T, et al. (2023) GBA1 in Parkinson's disease: variant detection and pathogenicity scoring matters. Bmc Genomics. 24: 322 |
| Vollstedt EJ, Schaake S, Lohmann K, et al. (2023) Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement Disorders : Official Journal of the Movement Disorder Society |
| Trinh J, Hicks AA, König IR, et al. (2022) Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's disease. Brain : a Journal of Neurology |