World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
67
Citations
24960
World Ranking
2496
National Ranking
83

Ryan D. Morin 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 Ryan D. Morin 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: 234 publications — 62nd percentile

62% of scientists in this discipline score the same or lower.

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

Ryan D. Morin 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 Ryan D. Morin 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: 67 D-Index — 43rd percentile

43% of scientists in this discipline score the same or lower.

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

Overview

Ryan D. Morin is affiliated with Simon Fraser University in Canada. Their research spans multiple areas within medicine and molecular biology, with a focus on hematology and oncology. The primary fields of study include Medicine and Biochemistry, Genetics and Molecular Biology.

The subfields of study they contribute to cover Pathology and Forensic Medicine, Molecular Biology, Genetics, Oncology, and Cancer Research. Morin's work is deeply connected to topics such as Lymphoma Diagnosis and Treatment, Chronic Lymphocytic Leukemia Research, Cancer Genomics and Diagnostics, CAR-T cell therapy research, Viral-associated cancers and disorders, Cancer-related gene regulation, and Monoclonal and Polyclonal Antibodies Research.

Frequent co-authors collaborating with Morin include:

  • David W. Scott
  • Laura K. Hilton
  • Christian Steidl
  • Kostiantyn Dreval
  • Pedro Farinha

Morin publishes regularly in a range of scientific journals, notably:

  • Blood
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Hematological Oncology
  • Blood Advances
  • Blood Cancer Discovery

Among the recent papers associated with Ryan D. Morin are:

  • "A Probabilistic Classification Tool for Genetic Subtypes of Diffuse Large B Cell Lymphoma with Therapeutic Implications," published in 2020 in Cancer Cell
  • "Genomic profiling for clinical decision making in lymphoid neoplasms," published in 2022 in Blood
  • "Super-enhancer hypermutation alters oncogene expression in B cell lymphoma," published in 2022 in Nature
  • "TBL1XR1 Mutations Drive Extranodal Lymphoma by Inducing a Pro-tumorigenic Memory Fate," published in 2020 in Cell
  • "Evaluating the quantity, quality and size distribution of cell-free DNA by multiplex droplet digital PCR," published in 2020 in Scientific Reports

The research papers demonstrate an involvement in genetic and molecular mechanisms underlying lymphoma and other hematological cancers, as well as advances in diagnostic techniques and clinical decision-making in lymphoid neoplasms.

Best Publications

  • Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

    Morin Rd;Johnson Na;Severson Tm;Mungall Aj

  • Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

    Ryan D Morin;María Méndez-Lago;Andrew J Mungall;Rodrigo Goya

  • Application of massively parallel sequencing to microRNA profiling and discovery in human embryonic stem cells.

    Ryan D Morin;Michael D O'Connor;Malachi Griffith;Florian Kuchenbauer

  • Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

    Sohrab P. Shah;Ryan D. Morin;Jaswinder Khattra;Leah Prentice

  • Genetic Alterations Activating Kinase and Cytokine Receptor Signaling in High-Risk Acute Lymphoblastic Leukemia

    Kathryn G. Roberts;Ryan D. Morin;Jinghui Zhang;Martin Hirst

  • Mutation of FOXL2 in Granulosa-Cell Tumors of the Ovary

    Sohrab P Shah;Martin Köbel;Janine Senz;Ryan D Morin

  • A Probabilistic Classification Tool for Genetic Subtypes of Diffuse Large B Cell Lymphoma with Therapeutic Implications.

    George W. Wright;Da Wei Huang;James D. Phelan;Zana A. Coulibaly

  • The complete genome of Rhodococcus sp. RHA1 provides insights into a catabolic powerhouse

    Michael P. McLeod;René L. Warren;William W. L. Hsiao;Naoto Araki

  • Identification of miR-145 and miR-146a as mediators of the 5q– syndrome phenotype

    Daniel T Starczynowski;Florian Kuchenbauer;Bob Argiropoulos;Sandy Sung

  • The status, quality, and expansion of the NIH full-length cDNA project: The Mammalian Gene Collection (MGC)

    Daniela S. Gerhard;Lukas Wagner;Elise A. Feingold;Carolyn M. Shenmen

  • Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation.

    Damian B. Yap;Damian B. Yap;Justin Chu;Tobias Berg;Matthieu Schapira

  • Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing.

    Ryan D. Morin;Matthew Bainbridge;Anthony Fejes;Martin Hirst

  • De novo transcriptome assembly with ABySS

    Inanç Birol;Shaun D. Jackman;Cydney B. Nielsen;Jenny Q. Qian

  • Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing.

    Ryan D. Morin;Ryan D. Morin;Karen Mungall;Erin Pleasance;Andrew J. Mungall

  • Next-generation tag sequencing for cancer gene expression profiling

    A Sorana Morrissy;Ryan D Morin;Allen Delaney;Thomas Zeng

  • Alternative expression analysis by RNA sequencing.

    Malachi Griffith;Malachi Griffith;Obi L Griffith;Obi L Griffith;Jill Mwenifumbo;Rodrigo Goya

  • Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma

    Robert Kridel;Robert Kridel;Barbara Meissner;Sanja Rogic;Merrill Boyle

  • Cell-free DNA (cfDNA): Clinical Significance and Utility in Cancer Shaped By Emerging Technologies.

    Stanislav Volik;Miguel Alcaide;Ryan D. Morin;Ryan D. Morin;Colin Collins;Colin Collins

  • Comparative analysis of the small RNA transcriptomes of Pinus contorta and Oryza sativa

    Ryan D. Morin;Gozde Aksay;Elena Dolgosheina;H. Alexander Ebhardt

  • Double-Hit Gene Expression Signature Defines a Distinct Subgroup of Germinal Center B-Cell-Like Diffuse Large B-Cell Lymphoma.

    Daisuke Ennishi;Aixiang Jiang;Merrill Boyle;Brett Collinge

Frequent Co-Authors

Marco A. Marra
Marco A. Marra University of British Columbia
Randy D. Gascoyne
Randy D. Gascoyne BC Cancer Agency
Christian Steidl
Christian Steidl University of British Columbia
Joseph M. Connors
Joseph M. Connors University of British Columbia
Steven J.M. Jones
Steven J.M. Jones University of British Columbia
Andrew J. Mungall
Andrew J. Mungall BC Cancer Agency
Sohrab P. Shah
Sohrab P. Shah Memorial Sloan Kettering Cancer Center
Martin Hirst
Martin Hirst University of British Columbia
David Scott
David Scott Ascension Health
Kerry J. Savage
Kerry J. Savage University of British Columbia

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Related Online Degrees & Career Pathways

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Another practical pivot is earning a medical billing and coding certification. This credential prepares graduates to process sensitive genetic data and medical records in healthcare settings. Each of these online pathways complements a background in genetics, expanding employment prospects across the healthcare industry.

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