World's Best Scientists 2026 revealed!
Kenneth Morgan

Kenneth Morgan

D-Index & Metrics

Genetics

D-Index
63
Citations
16678
World Ranking
2872
National Ranking
99

Kenneth Morgan 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 Kenneth Morgan 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: 151 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.

Kenneth Morgan 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 Kenneth Morgan 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: 63 D-Index — 35th percentile

35% of scientists in this discipline score the same or lower.

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

Overview

Kenneth Morgan was affiliated with McGill University in Canada. Their research primarily focused on medicine, with a notable emphasis on general health professions alongside specialized interests in artificial intelligence, computer vision and pattern recognition, public health, environmental and occupational health, and surgery.

Throughout their career, Morgan contributed to publications addressing various topics including:

  • AI in cancer detection
  • Handwritten text recognition techniques
  • Digital imaging in medicine
  • Abdominal trauma and injuries
  • Thermal regulation in medicine
  • Amoebic infections and treatments
  • Health sciences research and education

Some of Morgan's recent scholarly papers included:

  • A Method for Efficient De-identification of DICOM Metadata and Burned-in Pixel Text, 2024, Journal of Imaging Informatics in Medicine
  • Duke Spleen Data Set: A Publicly Available Spleen MRI and CT dataset for Training Segmentation, 2023, arXiv (Cornell University)
  • Duke Spleen Data Set, 2023, Zenodo (CERN European Organization for Nuclear Research)
  • Celebrating Ten Years of ECHO Ontario Chronic Pain and Opioid Stewardship, 2024, Pain Management

Their publications appeared in multiple venues, with repeated contributions to:

  • Zenodo (CERN European Organization for Nuclear Research)
  • Journal of Imaging Informatics in Medicine
  • arXiv (Cornell University)
  • Pain Management
  • Journal of the American Veterinary Medical Association

Frequent collaborators included Jacob A. Macdonald, Mustafa R. Bashir, Danielle Hom, Sarah Cubberley, and Kassi Sollace, each involved in several joint projects and publications.

Best Publications

  • Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

    A. Brooks-Wilson;M. Marcil;S. M. Clee;L.-H. Zhang

  • Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

    A Koufos;P Grundy;K Morgan;K A Aleck

  • SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis

    Clemens Bergwitz;Nicole M. Roslin;Martin Tieder;J.C. Loredo-Osti

  • Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy

    Sara J. Brown;Sara J. Brown;Sara J. Brown;Yuka Asai;Heather J. Cordell;Linda E. Campbell

  • Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

    F Rousseau;P Rouillard;M L Morel;E W Khandjian

  • ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF

    James C. Engert;Pierre Bérubé;Jocelyne Mercier;Carole Doré

  • Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.

    Jordan P Lerner-Ellis;Jamie C Tirone;Jamie C Tirone;Peter D Pawelek;Carole Doré

  • Imbalances in Dietary Consumption of Fatty Acids, Vegetables, and Fruits Are Associated With Risk for Crohn's Disease in Children

    Devendra K Amre;Savio D'Souza;Kenneth Morgan;Gillian Seidman

  • Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

    J. Simard;P. Tonin;F. Durocher;K. Morgan

  • Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles.

    C. Dombrowski;S. Lévesque;M. L. Morel;P. Rouillard

  • Allelic variation in TLR4 is linked to susceptibility to Salmonella enterica serovar Typhimurium infection in chickens.

    Gary Leveque;Vincenzo Forgetta;Shaun Morroll;Adrian L. Smith

  • Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene

    Patrick Frosk;Tracey Weiler;Edward Nylen;Thangirala Sudha

  • Haplotype mapping and sequence analysis of the mouse Nramp gene predict susceptibility to infection with intracellular parasites.

    Danielle Malo;Kyle Vogan;Silvia Vidal;Jinxin Hu

  • A survey of genetic and epigenetic variation affecting human gene expression.

    Tomi Pastinen;Robert Sladek;Scott Gurd;Alya’a Sammak

  • Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11

    Paul Grundy;Alex Koufos;Kenneth Morgan;Frederick P. Li

  • Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

    Celia M.T. Greenwood;T. Mary Fujiwara;T. Mary Fujiwara;Lucy J. Boothroyd;Mark A. Miller

  • Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion

    Laura Montermini;Andrea Richeter;Kenneth Morgan;Cristina M. Justice

  • Molecular scanning of the human PPARα gene: association of the L162V mutation with hyperapobetalipoproteinemia

    Marie-Claude Vohl;Pierre Lepage;Daniel Gaudet;Carl G. Brewer

  • Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene.

    Jing Liu;T.M. Fujiwara;N.T. Buu;F.O. Sanchez

  • Mutations in ABC1 in Tangier disease and familial high-density lipoprotein

    A Brooks-Wilson;Michel Marcil;Susanne M. Clee;Lin-Hua Zhang

Frequent Co-Authors

Thomas J. Hudson
Thomas J. Hudson Ontario Institute for Cancer Research
Ernest G. Seidman
Ernest G. Seidman McGill University
Emile Levy
Emile Levy University of Montreal
David R. Mack
David R. Mack University of Ottawa
Steven A. Narod
Steven A. Narod University of Toronto
Celia M. T. Greenwood
Celia M. T. Greenwood McGill University
Patricia N. Tonin
Patricia N. Tonin McGill University
Philippe Gros
Philippe Gros McGill University
Gustavo Turecki
Gustavo Turecki Douglas Mental Health University Institute
Guy A. Rouleau
Guy A. Rouleau Montreal Neurological Institute and Hospital

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Related Online Degrees & Career Pathways

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These online options provide greater flexibility, affordability, and a variety of career pathways for students with an interest in genetics and healthcare.

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