Matthew Farrer, PhD, Imperial College

Affiliations: 
Neurogenetics and Translational Medicine University of British Columbia, Vancouver, Vancouver, BC, Canada 
Area:
Neurodegenerative diseases
Website:
http://www.cmmt.ubc.ca/research/investigators/farrer/lab
Google:
"Matthew Farrer"
Cross-listing: Neurotree

Children

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Igor Tatarnikov grad student 2015- UBC (FlyTree)
Stefano Cataldi grad student 2014-2018 UBC (FlyTree)
Bahareh Behrouz post-doc 2008-2010 Mayo Clinic Jacksonville (Neurotree)
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Publications

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Lai D, Alipanahi B, Fontanillas P, et al. (2021) Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology
Farrer MJ, Bardien S, Hattori N, et al. (2021) Editorial: Celebrating the Diversity of Genetic Research to Dissect the Pathogenesis of Parkinson's Disease. Frontiers in Neurology. 12: 648417
Bentley SR, Guella I, Sherman HE, et al. (2021) Hunting for Familial Parkinson's Disease Mutations in the Post Genome Era. Genes. 12
Kuhlmann N, Wagner Valladolid M, Quesada-Ramírez L, et al. (2021) Chronic and Acute Manipulation of Cortical Glutamate Transmission Induces Structural and Synaptic Changes in Co-cultured Striatal Neurons. Frontiers in Cellular Neuroscience. 15: 569031
Bu M, Farrer MJ, Khoshbouei H. (2021) Dynamic control of the dopamine transporter in neurotransmission and homeostasis. Npj Parkinson's Disease. 7: 22
Follett J, Farrer MJ. (2021) LRRK2; a dynamic regulator of cellular trafficking. Brain Research. 1761: 147394
Robert J, Weilinger NL, Cao LP, et al. (2020) An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases. Molecular Neurodegeneration. 15: 70
Lin CH, Tsai PI, Lin HY, et al. (2020) Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy. Brain : a Journal of Neurology
Lüth T, König IR, Grünewald A, et al. (2020) Age at Onset of LRRK2 p.Gly2019Ser Is Related to Environmental and Lifestyle Factors. Movement Disorders : Official Journal of the Movement Disorder Society
Brown EE, Blauwendraat C, Trinh J, et al. (2020) Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease. Neurobiology of Aging
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