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D-Index & Metrics

Genetics

D-Index
77
Citations
41189
World Ranking
1735
National Ranking
796

Gary P. Schroth 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 Gary P. Schroth 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: 160 publications — 34th percentile

34% of scientists in this discipline score the same or lower.

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

Gary P. Schroth 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 Gary P. Schroth 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: 77 D-Index — 60th percentile

60% of scientists in this discipline score the same or lower.

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

Overview

Gary P. Schroth is affiliated with Illumina in the United States and has contributed extensively to research in biochemistry, genetics, molecular biology, and medicine. Their work spans several subfields including molecular biology, cancer research, infectious diseases, epidemiology, and genetics. The scientist's main research topics focus on cancer-related molecular mechanisms, RNA modifications and cancer, genomics and phylogenetic studies, SARS-CoV-2 and COVID-19 research, molecular biology techniques and applications, cancer genomics and diagnostics, and respiratory viral infections research.

The scientist has published in various venues, with the most frequent being:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Biotechnology
  • Scientific Reports
  • Nature Communications
  • UNC Libraries

Notable recent papers include:

  • Genome Sequencing of Sewage Detects Regionally Prevalent SARS-CoV-2 Variants, 2021, mBio
  • Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing, 2021, Nature Biotechnology
  • The RNA Atlas expands the catalog of human non-coding RNAs, 2021, Nature Biotechnology
  • Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study, 2021, Nature Biotechnology
  • Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing, 2021, Nature Biotechnology

Frequent co-authors collaborating with Gary P. Schroth include:

  • Scott Kuersten
  • Jo Vandesompele
  • Pieter Mestdagh
  • Justine Nuytens
  • Jasper Anckaert

Best Publications

  • Alternative Isoform Regulation in Human Tissue Transcriptomes

    Eric T. Wang;Rickard Sandberg;Rickard Sandberg;Shujun Luo;Irina Khrebtukova

  • Accurate whole human genome sequencing using reversible terminator chemistry

    David R. Bentley;Shankar Balasubramanian;Harold P. Swerdlow;Harold P. Swerdlow;Geoffrey P. Smith

  • The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements

    Leming Shi;Laura H. Reid;Wendell D. Jones;Richard Shippy

  • High density DNA methylation array with single CpG site resolution

    Marina Bibikova;Bret Barnes;Chan Tsan;Vincent Ho

  • Full-length mRNA-Seq from single-cell levels of RNA and individual circulating tumor cells

    Daniel Ramsköld;Shujun Luo;Yu Chieh Wang;Robin Li

  • Metagenomic discovery of biomass-degrading genes and genomes from cow rumen.

    Matthias Hess;Matthias Hess;Alexander Sczyrba;Alexander Sczyrba;Rob Egan;Rob Egan;Tae Wan Kim

  • A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium

    Zhenqiang Su;Paweł P. Łabaj;Sheng Li;Jean Thierry-Mieg

  • Global identification of microRNA-target RNA pairs by parallel analysis of RNA ends.

    Marcelo A German;Manoj Pillay;Dong-Hoon Jeong;Amit Hetawal

  • Mammalian microRNAs: experimental evaluation of novel and previously annotated genes

    H. Rosaria Chiang;Lori W. Schoenfeld;J. Graham Ruby;Vincent C. Auyeung

  • Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing

    Callum J. Bell;Darrell L. Dinwiddie;Darrell L. Dinwiddie;Neil A. Miller;Neil A. Miller;Shannon L. Hateley

  • Evaluation of quantitative miRNA expression platforms in the microRNA quality control (miRQC) study

    Pieter Mestdagh;Nicole Hartmann;Lukas Baeriswyl;Ditte Andreasen

  • PRG-1 and 21U-RNAs interact to form the piRNA complex required for fertility in C. elegans.

    Pedro J. Batista;J. Graham Ruby;Julie M. Claycomb;H. Rosaria Chiang

  • High-Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain

    Christopher Gregg;Jiangwen Zhang;Brandon Weissbourd;Brandon Weissbourd;Shujun Luo

  • Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis.

    Sergio E. Baranzini;Joann Mudge;Jennifer C. Van Velkinburgh;Pouya Khankhanian

  • From single-cell to cell-pool transcriptomes: Stochasticity in gene expression and RNA splicing

    Georgi K Marinov;Brian A Williams;Kenneth McCue;Gary P Schroth

  • Molecular Evidence of Sexual Transmission of Ebola Virus

    Suzanne E Mate;Jeffrey R Kugelman;Tolbert G Nyenswah;Jason T Ladner

  • Transcriptome-wide Regulation of Pre-mRNA Splicing and mRNA Localization by Muscleblind Proteins

    Eric T. Wang;Neal A.L. Cody;Sonali Jog;Michela Biancolella

  • Multiplexed RNA structure characterization with selective 2′-hydroxyl acylation analyzed by primer extension sequencing (SHAPE-Seq)

    Julius B. Lucks;Stefanie A. Mortimer;Cole Trapnell;Cole Trapnell;Shujun Luo

  • Cohesin‐mediated interactions organize chromosomal domain architecture

    Sevil Sofueva;Eitan Yaffe;Wen-Ching Chan;Dimitra Georgopoulou

  • Chimeric transcript discovery by paired-end transcriptome sequencing

    Christopher A. Maher;Nallasivam Palanisamy;John C. Brenner;Xuhong Cao

Frequent Co-Authors

Shujun Luo
Shujun Luo Predicine
Jo Vandesompele
Jo Vandesompele Ghent University
Pieter Mestdagh
Pieter Mestdagh Ghent University
Stephen F. Kingsmore
Stephen F. Kingsmore Rady Children's Hospital-San Diego
Rickard Sandberg
Rickard Sandberg Karolinska Institute
Christopher E. Mason
Christopher E. Mason Cornell University
Jennifer A. Doudna
Jennifer A. Doudna University of California, Berkeley
Joann Mudge
Joann Mudge National Center for Genome Resources
Yan W. Asmann
Yan W. Asmann Mayo Clinic
Adam P. Arkin
Adam P. Arkin Lawrence Berkeley National Laboratory

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