Matthew J. Farrer

University of Florida — United States

Medicine · Health Sciences

101h-index46.2kcitations531works5.52yr avg
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Research Topics

Parkinson's Disease Mechanisms and Treatments(391), Neurological diseases and metabolism(153), Nuclear Receptors and Signaling(119), Neurological disorders and treatments(87), RNA regulation and disease(64)

Publications529 total

A case report of multiple system atrophy-mimics: Importance of comprehensive evaluation in suspected familial cases
Medicine·2026Open Access
TDP-43 loss of function drives aberrant splicing in Parkinson’s disease
2025Open Access
Peripheral inflammation mediates midbrain Lrrk2 kinase activity via Rab32 expression
2025Open Access
Complementarity of long-read sequencing and optical genome mapping in Parkinson’s disease
2025Open Access
Genetic testing for <i>SCA27B</i> in Korean multiple system atrophy
Brain·2025Open Access
The age at onset of LRRK2 p.Gly2019Ser Parkinson’s disease across ancestries and countries of origin
2025Open Access
Central biogenic amine deficiency with concomitant exploratory behavioral deficits in Dnajc12 knock-out mice
npj Parkinson s Disease·2025· 1 citedOpen Access
Intronic <i>FGF14</i> GAA repeat expansions impact progression and survival in multiple system atrophy
Brain·2025· 4 citedOpen Access
Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin Reductase
International Journal of Molecular Sciences·2025Open Access
The Genetic Epidemiology of Parkinson's Disease view
The Lancet Neurology·2025· 1 cited
Genetic testing for <i>SCA27B</i> in Korean Multiple System Atrophy
2024Open Access
RAB32 mutation in Parkinson's disease – Author's reply
The Lancet Neurology·2024
Genome-wide association study of copy number variations in Parkinson’s disease
2024· 2 citedOpen Access
Characterization of <i>Dnajc12</i> knock-out mice, a model of hypodopaminergia
2024· 2 citedOpen Access
Association of Body Mass Index and Parkinson Disease
Neurology·2024· 9 citedOpen Access
The Evolution of Genetic Variability at the LRRK2 Locus
Genes·2024· 2 citedOpen Access
Genome-wide determinants of mortality and motor progression in Parkinson’s disease
npj Parkinson s Disease·2024· 14 citedOpen Access
Immunophenotyping Tracks Motor Progression in Parkinson’s Disease Associated with a TH Mutation
Journal of Parkinson s Disease·2024· 2 citedOpen Access
Newly discovered genetic variant that causes Parkinson’s disease clarifies why the condition develops and how to halt it
2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses
The Lancet Neurology·2024· 97 citedOpen Access
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Frequent Co-authors

Mary Hulihan(15), Jennifer M. Kachergus(14), Dennis W. Dickson(14), Zbigniew K. Wszołek(14), John Hardy(13), Owen A. Ross(13), Sarah Lincoln(12), Demetrius M. Maraganore(10), Ryan J. Uitti(9), Thomas Gasser(9), Jan Aasly(9), Andrew Singleton(8), A. Jon Stoessl(7), Carles Vilariño‐Güell(7), Katrina Gwinn(6), Ignácio F. Mata(6), Justus C. Dächsel(6), Ruey‐Meei Wu(6), S. Lincoln(5), Donald B. Calne(5)