World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
64
Citations
16831
World Ranking
2776
National Ranking
347

Tom Strachan 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 Tom Strachan 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: 144 publications — 27th percentile

27% of scientists in this discipline score the same or lower.

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

Tom Strachan 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 Tom Strachan 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: 64 D-Index — 37th percentile

37% of scientists in this discipline score the same or lower.

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

Research.com Recognitions

  • 2006 - Fellow of the Royal Society of Edinburgh

Overview

Tom Strachan is affiliated with Newcastle University in the United Kingdom. The scientist's academic career includes recognition as a Fellow of the Royal Society of Edinburgh, an honor awarded in 2006.

While detailed records of research papers are not available, the notable accolade indicates engagement with the scientific community at a distinguished level.

Information regarding co-authors, specific publication venues, book publications, and detailed fields or subfields of study is not provided.

This profile presents the available facts without additional interpretation or speculation.

Best Publications

  • Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury ( T ) gene family

    Li Qy;Newbury-Ecob Ra;Newbury-Ecob Ra;Terrett Ja;Wilson Di

  • Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

    A. Sakuntabhai;V. Ruiz-Perez;S. Carter;N. Jacobsen

  • Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

    Mayada Tassabehji;Andrew P. Read;Valerie E. Newton;Rodney Harris

  • A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

    R Bashir;S Britton;T Strachan;S Keers

  • Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.

    Edgar A. Otto;Bernhard Schermer;Tomoko Obara;John F. O'Toole

  • NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome.

    Emma T Tonkin;Tzu-Jou Wang;Steven Lisgo;Michael J Bamshad

  • The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome

    Mark Clement-Jones;Simone Schiller;Ercole Rao;Rüdiger J. Blaschke

  • Downregulation of NANOG induces differentiation of human embryonic stem cells to extraembryonic lineages.

    Louise Hyslop;Miodrag Stojkovic;Lyle Armstrong;Theresia Walter

  • Keratin 16 and keratin 17 mutations cause pachyonychia congenita.

    W.H.I. McLean;E.L. Rugg;D.P. Lunny;S.M. Morley

  • Hailey–Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump

    Ralf Sudbrak;Joanna Brown;Carol Dobson-Stone;Simon Carter

  • SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development

    N.A Hanley;D.M Hagan;M Clement-Jones;S.G Ball

  • Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse

    David Morgan;Lee Turnpenny;Judith Goodship;Weilie Dai

  • An Autogeneic Feeder Cell System That Efficiently Supports Growth of Undifferentiated Human Embryonic Stem Cells

    Petra Stojkovic;Majlinda Lako;Rebecca Stewart;Stefan Przyborski

  • A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

    Alison J. Ross;Victor Ruiz-Perez;Yiming Wang;Donna Marie Hagan

  • Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2.

    May Tassabehji;Andrew P. Read;Valerie E. Newton;Michael Patton

  • Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations.

    D. G R Evans;L. Trueman;A. Wallace;S. Collins

  • A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy Maps to Chromosome 2p

    R. Bashir;T. Strachan;S. Keers;A. Stephenson

  • Autosomal dominant sacral agenesis: Currarino syndrome

    Sally Ann Lynch;Yiming Wang;T Strachan;John Burn

  • Derivation of human embryonic stem cells from day-8 blastocysts recovered after three-step in vitro culture.

    Miodrag Stojkovic;Majlinda Lako;Petra Stojkovic;Rebecca Stewart

  • A genetic study oftype2neurofibromatosi s in theUnitedKingdom. I.Prevalence, mutation rate,fitness, andconfirmation ofmaternal transmission effect on severity

    D G R Evans;SM Huson;D Donnai;W Neary

Frequent Co-Authors

Susan Lindsay
Susan Lindsay Newcastle University
Majlinda Lako
Majlinda Lako Newcastle University
Stephen C. Robson
Stephen C. Robson Newcastle University
Judith A. Goodship
Judith A. Goodship Newcastle University
Sally Ann Lynch
Sally Ann Lynch University College Dublin
John Burn
John Burn Newcastle University
Jonathan L. Rees
Jonathan L. Rees University of Edinburgh
Peter J. Scambler
Peter J. Scambler University College London
Alain Hovnanian
Alain Hovnanian Imagine Institute for Genetic Diseases
Anthony P. Monaco
Anthony P. Monaco Tufts University

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