World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
56
Citations
12038
World Ranking
3494
National Ranking
417

Gavin Hudson 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 Gavin Hudson 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: 132 publications — 22nd percentile

22% of scientists in this discipline score the same or lower.

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

Gavin Hudson 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 Gavin Hudson 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: 56 D-Index — 21st percentile

21% of scientists in this discipline score the same or lower.

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

Overview

Gavin Hudson is affiliated with Newcastle University in the United Kingdom. Their research predominantly focuses on the field of Biochemistry, Genetics and Molecular Biology, with a total of 67 publications. Within this main discipline, they have contributed extensively to Molecular Biology, Clinical Biochemistry, and Neurology, alongside work in Cellular and Molecular Neuroscience and Cancer Research.

Their research addresses several key topics, which include:

  • Mitochondrial Function and Pathology
  • Metabolism and Genetic Disorders
  • Parkinson's Disease Mechanisms and Treatments
  • Metabolomics and Mass Spectrometry Studies
  • RNA modifications and cancer
  • Genetic Neurodegenerative Diseases
  • Single-cell and spatial transcriptomics

Gavin Hudson has authored numerous scientific papers, with some recent notable publications as follows:

  • Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesis, 2020, Nature Cancer
  • GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10-Year Population-Based Study, 2022, Movement Disorders
  • Circulating cell-free mitochondrial DNA levels in Parkinson's disease are influenced by treatment, 2020, Molecular Neurodegeneration
  • The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines, 2021, The Journal of Pathology
  • Heteroplasmic mitochondrial DNA variants in cardiovascular diseases, 2022, PLoS Genetics

The scientist frequently publishes in several journals including:

  • Scientific Reports
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Movement Disorders
  • npj Parkinson's Disease
  • Nature Cancer

Their collaborative network includes frequent co-authors such as:

  • Angela Pyle
  • Douglass M. Turnbull
  • Amy E. Vincent
  • Alexander G. Bury
  • Paolo Actis

Best Publications

  • Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

    Gavin Hudson;Patrizia Amati-Bonneau;Emma L. Blakely;Joanna D. Stewart

  • Characterizing mild cognitive impairment in incident Parkinson disease The ICICLE-PD Study

    Alison J Yarnall;David P Breen;Gordon W Duncan;Tien K Khoo

  • Inherited mitochondrial optic neuropathies

    Patrick Yu-Wai-Man;Philip G Griffiths;Gavin Hudson;Patrick F Chinnery

  • Multi-system neurological disease is common in patients with OPA1 mutations

    Patrick Yu-Wai-Man;Philip G. Griffiths;Philip G. Griffiths;G. Gorman;C.-M. Lourenco

  • Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease

    L.A. Robak;L.A. Robak;I.E. Jansen;I.E. Jansen;J van Rooij;A.G. Uitterlinden

  • Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

    Suzanne Lesage;Valérie Drouet;Elisa Majounie;Vincent Deramecourt

  • Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene

    R Horvath;G Hudson;G Ferrari;N Futterer

  • Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected by the Mitochondrial DNA–Haplogroup Background

    Gavin Hudson;Valerio Carelli;Valerio Carelli;Liesbeth Spruijt;Mike Gerards

  • Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

    A. Beilina;I. N. Rudenko;A. Kaganovich;L. Civiero

  • Whole-genome sequencing of patients with rare diseases in a national health system

    Ernest Turro;William J Astle;Karyn Megy;Stefan Graf

  • A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease

    V. Plagnol;M.A. Nalls;J.M. Bras;D.G. Hernandez;D.G. Hernandez

  • Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.

    Carla Giordano;Luisa Iommarini;Luca Giordano;Alessandra Maresca

  • Mitochondrial DNA polymerase-γ and human disease

    Gavin Hudson;Patrick F. Chinnery

  • Mutant POLG2 Disrupts DNA Polymerase γ Subunits and Causes Progressive External Ophthalmoplegia

    Matthew J. Longley;Susanna Clark;Cynthia Yu Wai Man;Gavin Hudson

  • A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy

    Debbie Hicks;A Sarkozy;N Muelas;K Koehler

  • Reduced mitochondrial DNA copy number is a biomarker of Parkinson's disease

    Angela Pyle;Haidyan Anugrha;Marzena Kurzawa-Akanbi;Alison Yarnall

  • Epigenetics, epidemiology and mitochondrial DNA diseases

    Patrick Francis Chinnery;Hannah R Elliott;Gavin Hudson;David C Samuels

  • Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder

    Gavin Hudson;Sharon Keers;Patrick Yu Wai Man;Philip Griffiths

  • Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene. Commentary

    Salvatore Dimauro;Guido Davidzon;Michio Hirano;Rita Horvath

  • Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

    C. C. Spencer;V. Plagnol;A. Strange;M. Gardner

Frequent Co-Authors

Patrick F. Chinnery
Patrick F. Chinnery University of Cambridge
Angela Pyle
Angela Pyle Newcastle University
Robert W. Taylor
Robert W. Taylor Newcastle University
David J. Burn
David J. Burn Newcastle University
Rita Horvath
Rita Horvath University of Cambridge
Douglass M. Turnbull
Douglass M. Turnbull Newcastle University
Patrick Yu-Wai-Man
Patrick Yu-Wai-Man University of Cambridge
Hanns Lochmüller
Hanns Lochmüller University of Freiburg
Massimo Zeviani
Massimo Zeviani University of Padua
Robert McFarland
Robert McFarland Newcastle University

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