World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
54
Citations
10694
World Ranking
3645
National Ranking
430

John A.L. Armour 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 John A.L. Armour 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: 135 publications — 23rd percentile

23% of scientists in this discipline score the same or lower.

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

John A.L. Armour 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 John A.L. Armour 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

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Mutation

His primary areas of study are Genetics, Gene, Genome, Allele and Copy-number variation. Genomic DNA, Locus, Angelman syndrome, Tandem repeat and Minisatellite are among the areas of Genetics where the researcher is concentrating his efforts. His study explores the link between Minisatellite and topics such as Genetic variation that cross with problems in Genetic marker.

His studies deal with areas such as Molecular biology and Psoriasis as well as Gene. His Allele research is multidisciplinary, incorporating perspectives in Immunohistochemistry, Tissue sections, Pathology, Breast tumours and Retinoblastoma gene. His Copy-number variation study combines topics in areas such as Gene cluster, Genome-wide association study and Polymerase chain reaction.

His most cited work include:

  • Psoriasis is associated with increased beta-defensin genomic copy number. (545 citations)
  • Complex gene conversion events in germline mutation at human minisatellites (465 citations)
  • Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis (427 citations)

What are the main themes of his work throughout his whole career to date?

His scientific interests lie mostly in Genetics, Minisatellite, Locus, Allele and Copy-number variation. His study in Gene, Minisatellite Repeat, Human genome, Genetic marker and Tandem repeat falls within the category of Genetics. John A.L. Armour works mostly in the field of Minisatellite, limiting it down to concerns involving Evolutionary biology and, occasionally, Genetic variation.

His research in Locus intersects with topics in genomic DNA and Molecular biology. His research investigates the connection with Allele and areas like Germline mutation which intersect with concerns in Germline. His study in Copy-number variation is interdisciplinary in nature, drawing from both Polymerase chain reaction, Disease, Immunology and Haplotype.

He most often published in these fields:

  • Genetics (81.56%)
  • Minisatellite (26.95%)
  • Locus (26.24%)

What were the highlights of his more recent work (between 2009-2019)?

  • Genetics (81.56%)
  • Copy-number variation (24.82%)
  • Gene (20.57%)

In recent papers he was focusing on the following fields of study:

John A.L. Armour mainly focuses on Genetics, Copy-number variation, Gene, Haplotype and Locus. In his study, he carries out multidisciplinary Genetics and Amylase research. John A.L. Armour interconnects Comparative genomic hybridization, Disease, Genetic association and Polymerase chain reaction in the investigation of issues within Copy-number variation.

His work on Gene cluster and Gene duplication is typically connected to HRAS and MSH2 as part of general Gene study, connecting several disciplines of science. His Haplotype research integrates issues from Evolutionary biology, Structural variation, Computational biology and Human genome. His Locus research incorporates themes from Fixation, Low copy number, Allele frequency and Genetic variation.

Between 2009 and 2019, his most popular works were:

  • Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies (108 citations)
  • α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects (96 citations)
  • Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. (82 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Genetics

His primary areas of investigation include Genetics, Gene, Human genome, Copy-number variation and Amylase. As part of his studies on Genetics, he often connects relevant areas like Odds ratio. In general Gene study, his work on Mutation, Mutant and Point mutation often relates to the realm of Myofibril assembly and MYH6, thereby connecting several areas of interest.

His studies in Human genome integrate themes in fields like Polymorphism, CCL3L1, Disease, Human genetics and Polymerase chain reaction. Many of his studies on Copy-number variation involve topics that are commonly interrelated, such as Haplotype. He has researched Locus in several fields, including Young adult, Meta-analysis, Epistasis and Immunology.

Best Publications

  • Psoriasis is associated with increased beta-defensin genomic copy number.

    Edward J Hollox;Ulrike Huffmeier;Patrick L J M Zeeuwen;Raquel Palla

  • Complex gene conversion events in germline mutation at human minisatellites

    Alec J. Jeffreys;Keiji Tamaki;Annette MacLeod;Darren G. Monckton;Darren G. Monckton

  • Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis

    Rafael De Cid;Eva Riveira-Munoz;Patrick L.J.M. Zeeuwen;Jason Robarge

  • Isolation of human simple repeat loci by hybridization selection

    John A.L. Armour;Rita Neumann;Stephanie Gobert;Alec J. Jeffreys

  • Extensive Normal Copy Number Variation of a β-Defensin Antimicrobial-Gene Cluster

    Edward J. Hollox;John A. L. Armour;John C. K. Barber;John C. K. Barber

  • Uniparental paternal disomy in Angelman's syndrome

    S. Malcolm;J. Clayton-Smith;M. Nichols;M.E. Pembrey

  • The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

    Maria J. Mascari;Wayne Gottlieb;Peter K. Rogan;Merlin G. Butler

  • Measurement of locus copy number by hybridisation with amplifiable probes

    John A. L. Armour;Carolina Sismani;Philippos C. Patsalis;Gareth Cross

  • The retinoblastoma gene is frequently altered leading to loss of expression in primary breast tumours.

    Varley Jm;Armour J;Swallow Je;Jeffreys Aj

  • Genomic copy number variation, human health, and disease.

    Louise V Wain;John A L Armour;Martin D Tobin

  • Minisatellite diversity supports a recent African origin for modern humans

    John A.L. Armour;John A.L. Armour;Tiiu Anttinen;Celia A. May;Emilce E. Vega

  • Copy number polymorphism and expression level variation of the human α-defensin genes DEFA1 and DEFA3

    Patricia M.R. Aldred;Edward J. Hollox;John A.L. Armour

  • β-Defensin-2 Protein Is a Serum Biomarker for Disease Activity in Psoriasis and Reaches Biologically Relevant Concentrations in Lesional Skin

    Patrick A. M. Jansen;Diana Rodijk-Olthuis;Edward J. Hollox;Marijke Kamsteeg

  • Systematic cloning of human minisatellites from ordered array charomid libraries.

    John A.L. Armour;Sue Povey;Stephen Jeremiah;Alec J. Jeffreys

  • Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.

    Beth Coyle;Rebecca Coffey;John A.L. Armour;Eleanor Gausden

  • Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy.

    Jannine Clapp;Laura M. Mitchell;Daniel J. Bolland;Judy Fantes

  • Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats

    John A. L. Armour;Raquel Palla;Patrick L. J. M. Zeeuwen;Martin den Heijer

  • α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

    Javier T. Granados-Riveron;Tushar K. Ghosh;Mark Pope;Frances Bu'Lock

  • The detection of large deletions or duplications in genomic DNA.

    J.A.L. Armour;D.E. Barton;D.J. Cockburn;G.R. Taylor

  • Sequences flanking the repeat arrays of human minlsatellites: association with tandem and dispersed repeat elements

    John A.L. Armour;Zilla Wong;Victoria Wilson;Nicola J. Royle

Frequent Co-Authors

Alec J. Jeffreys
Alec J. Jeffreys University of Leicester
Joost Schalkwijk
Joost Schalkwijk Radboud University
Patrick L.J.M. Zeeuwen
Patrick L.J.M. Zeeuwen Radboud University
Martin den Heijer
Martin den Heijer University of Amsterdam
Darren G. Monckton
Darren G. Monckton University of Glasgow
James T. Elder
James T. Elder University of Michigan–Ann Arbor
André Reis
André Reis University of Erlangen-Nuremberg
Mathias M. Siems
Mathias M. Siems European University Institute
Richard C. Trembath
Richard C. Trembath King's College London

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