World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
54
Citations
69687
World Ranking
3599
National Ranking
1558

Matthew N. Bainbridge 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 Matthew N. Bainbridge 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: 111 publications — 12th percentile

12% of scientists in this discipline score the same or lower.

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

Matthew N. Bainbridge 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 Matthew N. Bainbridge 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

Matthew N. Bainbridge is affiliated with Rady Children's Hospital-San Diego in the United States. Their research primarily spans the fields of biochemistry, genetics, and molecular biology, with significant contributions to medicine. The scientist's work is concentrated in the subfields of molecular biology, genetics, oncology, cancer research, and pathology and forensic medicine.

The main topics of research undertaken by Bainbridge include genomics and rare diseases, genetics and neurodevelopmental disorders, DNA repair mechanisms, PARP inhibition in cancer therapy, cancer genomics and diagnostics, genetic factors in colorectal cancer, and genomics and phylogenetic studies.

Frequent coauthors collaborating with Bainbridge are:

  • Erica Sanford Kobayashi
  • Stephen F. Kingsmore
  • Aloran Mazumder
  • Svasti Haricharan
  • Jennifer Friedman

Bainbridge has published articles in multiple scientific venues, notably:

  • Cancer Research
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genetics in Medicine Open
  • Science Advances
  • Brain

Representative recent papers authored or coauthored by Bainbridge include:

  • "Approaches to long-read sequencing in a clinical setting to improve diagnostic rate" (2022, Scientific Reports)
  • "POT1 mutation spectrum in tumour types commonly diagnosed among POT1-associated hereditary cancer syndrome families" (2020, Journal of Medical Genetics)
  • "The genomic landscape of familial glioma" (2023, Science Advances)
  • "Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing" (2023, JAMA Network Open)
  • "Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder" (2020, Human Molecular Genetics)

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • An integrated map of genetic variation from 1,092 human genomes

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • Table S2: Trans-factors and trinucleotide repeat instability Trans-factor

    Arturo López Castel;John D Cleary;Christopher E Pearson

  • Comprehensive molecular characterization of human colon and rectal cancer

    Donna M. Muzny;Matthew N. Bainbridge;Kyle Chang;Huyen H. Dinh

  • Clinical whole-exome sequencing for the diagnosis of mendelian disorders.

    Yaping Yang;Donna M. Muzny;Jeffrey G. Reid;Matthew N. Bainbridge

  • Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing

    Gordon Robertson;Martin Hirst;Matthew Bainbridge;Misha Bilenky

  • Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

    Yaping Yang;Donna M. Muzny;Fan Xia;Zhiyv Niu

  • Mapping copy number variation by population-scale genome sequencing

    Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy

    James R. Lupski;Jeffrey G. Reid;Claudia Gonzaga-Jauregui;David Rio Deiros

  • A map of human genome variation from population-scale sequencing

    Richard M. Durbin;David L. Altshuler;Gonçalo R. Abecasis;David R. Bentley

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

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

  • FindPeaks 3.1

    Anthony P. Fejes;Gordon Robertson;Mikhail Bilenky;Richard Varhol

  • Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.

    Lauge Farnaes;Lauge Farnaes;Amber Hildreth;Amber Hildreth;Nathaly M. Sweeney;Nathaly M. Sweeney;Michelle M. Clark

  • Whole-Genome Sequencing for Optimized Patient Management

    Matthew N. Bainbridge;Wojciech Wiszniewski;David R. Murdock;Jennifer Friedman;Jennifer Friedman

  • A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.

    Stephen F. Kingsmore;Julie A. Cakici;Julie A. Cakici;Michelle M. Clark;Mary Gaughran

  • Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approach

    Matthew N. Bainbridge;René L. Warren;Martin Hirst;Tammy Romanuik

  • Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy

    Claudia Gonzaga-Jauregui;Claudia Gonzaga-Jauregui;Tamar Harel;Tomasz Gambin;Maria Kousi

  • Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline.

    Jeffrey G. Reid;Andrew Carroll;Narayanan Veeraraghavan;Mahmoud Dahdouli

  • Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation

    Michelle M. Clark;Amber Hildreth;Amber Hildreth;Amber Hildreth;Sergey Batalov;Yan Ding

Frequent Co-Authors

Richard A. Gibbs
Richard A. Gibbs Baylor College of Medicine
Donna M. Muzny
Donna M. Muzny Baylor College of Medicine
Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
James R. Lupski
James R. Lupski Baylor College of Medicine
Jeffrey G. Reid
Jeffrey G. Reid Regeneron (United States)
Shalini N. Jhangiani
Shalini N. Jhangiani Baylor College of Medicine
Christine M. Eng
Christine M. Eng Baylor College of Medicine
Elaine R. Mardis
Elaine R. Mardis The Ohio State University
Christie L. Kovar
Christie L. Kovar Baylor College of Medicine
Arthur L. Beaudet
Arthur L. Beaudet Baylor College of Medicine

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