World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
54
Citations
26516
World Ranking
3605
National Ranking
428

Colin A. Semple 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 Colin A. Semple 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: 150 publications — 30th percentile

30% of scientists in this discipline score the same or lower.

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

Colin A. Semple 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 Colin A. Semple 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: 54 D-Index — 17th percentile

17% of scientists in this discipline score the same or lower.

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

Overview

Colin A. Semple is affiliated with the University of Edinburgh in the United Kingdom. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, with significant contributions to Medicine. Within these areas, their work focuses particularly on Molecular Biology, Genetics, Cancer Research, Reproductive Medicine, and Oncology.

The scientist's published work covers several specific topics, including Cancer Genomics and Diagnostics, DNA Repair Mechanisms, Ovarian Cancer Diagnosis and Treatment, PARP Inhibition in Cancer Therapy, Genomics and Rare Diseases, Genomics and Chromatin Dynamics, and BRCA Gene Mutations in Cancer.

Colin A. Semple has contributed extensively to various academic venues. Their frequent publication outlets include bioRxiv (Cold Spring Harbor Laboratory), where they have published 14 papers, Nature Communications with 6 papers, Genome Research and Clinical Cancer Research with 3 papers each, and Nature with 2 papers.

Several recent papers illustrate the focus of their research:

  • "A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns" (2020) in Nature Communications
  • "Functional annotation of human long noncoding RNAs via molecular phenotyping" (2020) in Genome Research
  • "Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome" (2020) in Nature Communications
  • "Sex differences in oncogenic mutational processes" (2020) in Nature Communications
  • "Pervasive lesion segregation shapes cancer genome evolution" (2020) in Nature

The scientist collaborates with a range of researchers, including Alison Meynert, Ailith Ewing, Vera B. Kaiser, Charlie Gourley, and Martin S. Taylor, each having coauthored multiple works with them.

Best Publications

  • The Transcriptional Landscape of the Mammalian Genome

    P. Carninci;T. Kasukawa;S. Katayama;J. Gough

  • Pan-cancer analysis of whole genomes

    Peter J. Campbell;Gad Getz;Jan O. Korbel;Joshua M. Stuart

  • Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

    Y. Okazaki;M. Furuno;T. Kasukawa;J. Adachi

  • A promoter-level mammalian expression atlas

    Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie

  • Genome-wide analysis of mammalian promoter architecture and evolution

    Piero Carninci;Albin Sandelin;Boris Lenhard;Boris Lenhard;Shintaro Katayama

  • Disruption of two novel genes by a translocation co-segregating with schizophrenia

    J. Kirsty Millar;Julie C. Wilson-Annan;Susan Anderson;Sheila Christie

  • Patterns of somatic structural variation in human cancer genomes

    Yilong Li;Nicola D Roberts;Jeremiah A Wala;Jeremiah A Wala;Ofer Shapira;Ofer Shapira

  • Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.

    Yanick J Crow;Yanick J Crow;Andrea Leitch;Bruce E Hayward;Anna Garner

  • Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

    Albert Tenesa;Susan M Farrington;James G D Prendergast;Mary E Porteous

  • A high-resolution anatomical atlas of the transcriptome in the mouse embryo.

    Graciana Diez-Roux;Sandro Banfi;Marc Sultan;Lars Geffers

  • Proteins containing the UBA domain are able to bind to multi-ubiquitin chains.

    Caroline R.M. Wilkinson;Michael Seeger;Rasmus Hartmann-Petersen;Miranda Stone

  • The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line

    Harukazu Suzuki;Alistair R.R. Forrest;Erik Van Nimwegen;Carsten O. Daub

  • Posttranscriptional regulation of miRNAs harboring conserved terminal loops.

    Gracjan Michlewski;Sonia Guil;Colin A. Semple;Javier F. Cáceres

  • Hierarchical folding and reorganization of chromosomes are linked to transcriptional changes in cellular differentiation

    James Fraser;Carmelo Ferrai;Carmelo Ferrai;Andrea M Chiariello;Markus Schueler

  • Conservation and divergence in Toll-like receptor 4-regulated gene expression in primary human versus mouse macrophages

    Kate Schroder;Katharine M Irvine;Martin S Taylor;Nilesh J Bokil

  • POCUS: mining genomic sequence annotation to predict disease genes

    Frances S Turner;Daniel R Clutterbuck;Colin A M Semple

  • Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

    Malcolm G Dunlop;Sara E Dobbins;Susan Mary Farrington;Angela M Jones

  • Two novel proteins recruited by synaptonemal complex protein 1 (SYCP1) are at the centre of meiosis

    Yael Costa;Robert Speed;Rupert Öllinger;Manfred Alsheimer

  • Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cells

    Nicola Reynolds;Brian Collier;Klio Maratou;Victoria Bingham

  • Duplication and selection in the evolution of primate β-defensin genes

    Colin A M Semple;Mark Rolfe;Julia R Dorin

Frequent Co-Authors

Martin S. Taylor
Martin S. Taylor Harvard University
David J. Porteous
David J. Porteous University of Edinburgh
Alistair R. R. Forrest
Alistair R. R. Forrest Harry Perkins Institute of Medical Research
Boris Lenhard
Boris Lenhard Imperial College London
Albin Sandelin
Albin Sandelin University of Copenhagen
David A. Hume
David A. Hume University of Queensland

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