World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
47
Citations
28476
World Ranking
4076
National Ranking
6

Russell G. Snell 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 Russell G. Snell 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: 138 publications — 24th percentile

24% of scientists in this discipline score the same or lower.

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

Russell G. Snell 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 Russell G. Snell 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: 47 D-Index — 6th percentile

6% of scientists in this discipline score the same or lower.

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

Overview

Russell G. Snell is affiliated with the University of Auckland in New Zealand and has a research portfolio primarily focused on biochemistry, genetics, and molecular biology with contributions extending into medicine. Their research spans several subfields including molecular biology, genetics, infectious diseases, cellular and molecular neuroscience, and physiology.

Snell's work covers a variety of specific topics such as:

  • CRISPR and genetic engineering
  • Animal genetics and reproduction
  • Genetic neurodegenerative diseases
  • Genetic and phenotypic traits in livestock
  • Mitochondrial function and pathology
  • Genetic mapping and diversity in plants and animals
  • Single-cell and spatial transcriptomics

The scientist has contributed to recent papers including:

  • From Pathogenesis to Therapeutics: A Review of 150 Years of Huntington's Disease Research, 2023, International Journal of Molecular Sciences
  • DNA methylation study of Huntington's disease and motor progression in patients and in animal models, 2020, Nature Communications
  • Castration delays epigenetic aging and feminizes DNA methylation at androgen-regulated loci, 2021, eLife
  • A Review of the Current Mammalian Models of Alzheimer's Disease and Challenges That Need to Be Overcome, 2021, International Journal of Molecular Sciences
  • Genome-wide association studies of lactation yields of milk, fat, protein and somatic cell score in New Zealand dairy goats, 2020, Journal of Animal Science and Biotechnology

Frequent publication venues for Snell's work include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genetics Selection Evolution
  • Expert Review of Clinical Immunology
  • International Journal of Molecular Sciences
  • eLife

Collaborations have been established with multiple coauthors, among them:

  • Klaus Lehnert
  • Jessie C. Jacobsen
  • Andrew Jiang
  • Renée R. Handley
  • Mathew D. Littlejohn

The scientist's research contributes to better understanding complex genetic mechanisms and molecular pathways, particularly in the context of neurodegenerative diseases like Huntington's and Alzheimer's, as well as in livestock genetics and reproductive biology.

Best Publications

  • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

    Marcy E. MacDonald;Christine M. Ambrose;Mabel P. Duyao;Richard H. Myers

  • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.

    M Shah;N Datson;L Srinidhi;VP Stanton

  • Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

    J. David Brook;Mila E. McCurrach;Helen G. Harley;Alan J. Buckler

  • Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34

    Marjon van Slegtenhorst;Ronald de Hoogt;Caroline Hermans;Mark Nellist

  • Positional candidate cloning of a QTL in dairy cattle: identification of a missense mutation in the bovine DGAT1 gene with major effect on milk yield and composition.

    Bernard Grisart;Wouter Coppieters;Frédéric Farnir;Latifa Karim

  • Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

    Russell G. Snell;John C. MacMillan;Jeremy Peter Cheadle;Iain Fenton

  • Interaction Between Hamartin and Tuberin, the TSC1 and TSC2 Gene Products

    Marjon van Slegtenhorst;Mark Nellist;Bas Nagelkerken;Jeremy Cheadle

  • Molecular dissection of a quantitative trait locus: a phenylalanine-to-tyrosine substitution in the transmembrane domain of the bovine growth hormone receptor is associated with a major effect on milk yield and composition.

    Sarah Blott;Jong-Joo Kim;Sirja Moisio;Anne Schmidt-Küntzel

  • Molecular Genetic and Phenotypic Analysis Reveals Differences between TSC1 and TSC2 Associated Familial and Sporadic Tuberous Sclerosis

    Alistair C. Jones;Claire E. Daniells;Russell G. Snell;Maria Tachataki

  • Characterization of the DGAT1 gene in the New Zealand dairy population

    R.J. Spelman;C.A. Ford;P. McElhinney;G.C. Gregory

  • Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

    Colby Chiang;Jessie C Jacobsen;Carl Ernst;Carrie Hanscom

  • An ovine transgenic Huntington's disease model

    Jessie C. Jacobsen;C. Simon Bawden;Skye R. Rudiger;Clive J. McLaughlan

  • Sequence-based Association Analysis Reveals an MGST1 eQTL with Pleiotropic Effects on Bovine Milk Composition.

    Mathew D. Littlejohn;Mathew D. Littlejohn;Kathryn Tiplady;Tania A. Fink;Klaus Lehnert

  • Hyperekplexia associated with compound heterozygote mutations in the β-subunit of the human inhibitory glycine receptor (GLRB)

    Mark I. Rees;Trevor M. Lewis;John B. J. Kwok;Geert R. Mortier

  • Functionally reciprocal mutations of the prolactin signalling pathway define hairy and slick cattle.

    Mathew D. Littlejohn;Kristen M. Henty;Kathryn Tiplady;Thomas Johnson

  • Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia

    Mark I. Rees;Kirsten Harvey;Hamish Ward;Julia H. White

  • Molecular analysis and clinical correlations of the Huntington's disease mutation

    J. C. MacMillan;R. G. Snell;A. Tyler;G. D. Houlihan

  • Mutation in Bovine β-Carotene Oxygenase 2 Affects Milk Color

    S. D. Berry;S. R. Davis;E. M. Beattie;N. L. Thomas

  • TATA-binding protein in neurodegenerative disease.

    W.M.C. van Roon-Mom;S.J. Reid;R.L.M. Faull;R.G. Snell

  • Molecular dissection of a quantitative trait locus: a phenylalanine-to-tyrosine substitution in the transmembrane domain of the bovine growth hormone receptor is associated with a major effect on milk yield and composition.

    Wouter Coppieters;Sarah C. Blott;Michel Georges;Richard J. Spelman

Frequent Co-Authors

Richard Spelman
Richard Spelman Livestock Improvement Corporation
Richard L.M. Faull
Richard L.M. Faull University of Auckland
Marcy E. MacDonald
Marcy E. MacDonald Harvard University
Henry J. Waldvogel
Henry J. Waldvogel University of Auckland
Mark I. Rees
Mark I. Rees Swansea University
Peter S. Harper
Peter S. Harper Cardiff University
James F. Gusella
James F. Gusella Harvard University
Joel H. Rothman
Joel H. Rothman University of California, Santa Barbara
Michael John Owen
Michael John Owen Cardiff University
Dorian J. Garrick
Dorian J. Garrick Massey University

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