World's Best Scientists 2026 revealed!

D-Index & Metrics

Medicine

D-Index
114
Citations
58151
World Ranking
4661
National Ranking
2532

Genetics

D-Index
108
Citations
52959
World Ranking
564
National Ranking
281

Matthew J. Farrer publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Matthew J. Farrer sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 431 publications — 90th percentile

90% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Matthew J. Farrer D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Matthew J. Farrer sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 108 D-Index — 87th percentile

87% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Overview

Matthew J. Farrer is affiliated with the University of Florida in the United States. Their research activity primarily focuses on various aspects of Parkinson's disease, including mechanisms, treatments, and related neurological processes. The scientist's work spans multiple disciplines such as medicine, biochemistry, genetics, molecular biology, and neuroscience.

Farrer's main fields of study include:

  • Medicine
  • Biochemistry, Genetics and Molecular Biology
  • Neuroscience

The subfields of study in which they have contributed notably are:

  • Neurology
  • Molecular Biology
  • Cellular and Molecular Neuroscience
  • Genetics
  • Physiology

The principal research topics covered in their publications are:

  • Parkinson's Disease Mechanisms and Treatments
  • Neurological diseases and metabolism
  • RNA regulation and disease
  • Nuclear Receptors and Signaling
  • Lysosomal Storage Disorders Research
  • Cellular transport and secretion
  • Neurological disorders and treatments

Frequently publishing in venues specializing in neurodegenerative diseases and neuroscience, Farrer's common publication outlets include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Brain
  • Movement Disorders
  • npj Parkinson s Disease
  • Research Square (Research Square)

Notable papers from Matthew J. Farrer include:

  • "The Gut-Brain Axis and Its Relation to Parkinson's Disease: A Review" (2022) in Frontiers in Aging Neuroscience
  • "Disease modification and biomarker development in Parkinson disease" (2020) in Neurology
  • "Variants in saposin D domain of prosaposin gene linked to Parkinson's disease" (2020) in Brain
  • "Dynamic control of the dopamine transporter in neurotransmission and homeostasis" (2021) in npj Parkinson s Disease
  • "RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses" (2024) in The Lancet Neurology

They have collaborated frequently with several researchers, including:

  • Jordan Follett
  • Joanne Trinh
  • Alexis Brice
  • Christine Klein
  • Nobutaka Hattori

Best Publications

  • α-Synuclein Locus Triplication Causes Parkinson's Disease

    A. B. Singleton;M. Farrer;J. Johnson;A. Singleton

  • Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

    Alexander Zimprich;Alexander Zimprich;Saskia Biskup;Petra Leitner;Peter Lichtner

  • α-synuclein locus duplication as a cause of familial Parkinson's disease

    Marie-Christine Chartier-Harlin;Jennifer M. Kachergus;Christophe Roumier;Vincent Mouroux

  • Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

    Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz

  • VPS35 Mutations in Parkinson Disease

    Carles Vilariño-Güell;Christian Wider;Owen A. Ross;Justus C. Dachsel

  • Missing pieces in the Parkinson's disease puzzle.

    Jose A Obeso;Maria C Rodriguez-Oroz;Christopher G Goetz;Concepcion Marin;Concepcion Marin

  • Genetics of Parkinson disease: paradigm shifts and future prospects.

    Matthew James Farrer

  • Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplications

    Matt Farrer;Jennifer Kachergus;Lysia Forno;Sarah Lincoln

  • Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease

    Silke Appel-Cresswell;Carles Vilarino-Guell;Mary Encarnacion;Holly Sherman

  • Parkin protects against the toxicity associated with mutant alpha-synuclein: proteasome dysfunction selectively affects catecholaminergic neurons.

    Leonard Petrucelli;Casey O'Farrell;Paul J. Lockhart;Melisa Baptista

  • α-Synuclein Shares Physical and Functional Homology with 14-3-3 Proteins

    Natalie Ostrerova;Leonard Petrucelli;Matthew Farrer;Nitinkumar Mehta

  • Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

    Günter U. Höglinger;Nadine M. Melhem;Dennis W. Dickson;Patrick M A Sleiman

  • Lewy bodies and parkinsonism in families with parkin mutations.

    M Farrer;P Chan;R Chen;L Tan

  • Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

    Jennifer Kachergus;Ignacio F. Mata;Mary Hulihan;Julie P. Taylor

  • Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

    Demetrius M. Maraganore;Mariza De Andrade;Alexis Elbaz;Matthew J. Farrer

  • High-Resolution Whole-Genome Association Study of Parkinson Disease

    Demetrius M. Maraganore;Mariza de Andrade;Timothy G. Lesnick;Kari J. Strain

  • Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database.

    Christina M. Lill;Johannes T. Roehr;Johannes T. Roehr;Matthew B. McQueen;Fotini K. Kavvoura;Fotini K. Kavvoura;Fotini K. Kavvoura

  • LRRK2 in Parkinson's disease: protein domains and functional insights.

    Ignacio F. Mata;William J. Wedemeyer;Matthew J. Farrer;Julie P. Taylor

  • Advances in the genetics of Parkinson disease

    Joanne Trinh;Matt Farrer

  • Molecular mapping of alzheimer-type dementia in Down's syndrome

    V. P. Prasher;Matthew J. Farrer;Anna M. Kessling;Elizabeth M. C. Fisher

Frequent Co-Authors

Owen A. Ross
Owen A. Ross Mayo Clinic
Sarah Lincoln
Sarah Lincoln Mayo Clinic
Ryan J. Uitti
Ryan J. Uitti Mayo Clinic
John Hardy
John Hardy University College London
Demetrius M. Maraganore
Demetrius M. Maraganore Tulane University
Thomas Gasser
Thomas Gasser University of Tübingen
Alexis Brice
Alexis Brice Institut du Cerveau
Nobutaka Hattori
Nobutaka Hattori Juntendo University

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