World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
55
Citations
14428
World Ranking
3559
National Ranking
1543

Gholson J. Lyon 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 Gholson J. Lyon 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: 257 publications — 68th percentile

68% of scientists in this discipline score the same or lower.

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

Gholson J. Lyon 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 Gholson J. Lyon 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: 55 D-Index — 19th percentile

19% 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

Gholson J. Lyon mainly focuses on Genetics, Exome sequencing, Exome, DNA sequencing and Genomics. Genetics and Enzyme are commonly linked in his work. Gholson J. Lyon combines subjects such as Acetyltransferase, Ogden Syndrome, Hypotonia, X chromosome and Exon with his study of Exome sequencing.

His Exome research incorporates elements of Genome, Whole genome sequencing, Sequence alignment and Indel. His DNA sequencing research incorporates themes from Data mining, Deep sequencing and Word error rate. His Genomics research includes themes of Ontology, Precision medicine, Translational research and Phenotype.

His most cited work include:

  • Analysis of shared heritability in common disorders of the brain (726 citations)
  • The Human Phenotype Ontology in 2017 (471 citations)
  • Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2 , a COX assembly gene (465 citations)

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

His scientific interests lie mostly in Genetics, Computational biology, Exome sequencing, Genome and Whole genome sequencing. All of his Genetics and DNA sequencing, Copy-number variation, Human genetics, Genomics and Personal genomics investigations are sub-components of the entire Genetics study. His Copy-number variation research is multidisciplinary, relying on both Genome-wide association study and Tourette syndrome.

His study in Exome sequencing is interdisciplinary in nature, drawing from both Hypotonia, Human Phenotype Ontology and Indel. The Genome study combines topics in areas such as Genotyping and Bioinformatics. His research investigates the link between Whole genome sequencing and topics such as Exome that cross with problems in Human genome.

He most often published in these fields:

  • Genetics (62.63%)
  • Computational biology (21.45%)
  • Exome sequencing (27.34%)

What were the highlights of his more recent work (between 2015-2021)?

  • Genetics (62.63%)
  • Exome sequencing (27.34%)
  • Tourette syndrome (9.34%)

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

Gholson J. Lyon spends much of his time researching Genetics, Exome sequencing, Tourette syndrome, Phenotype and Human Phenotype Ontology. His study in Copy-number variation, Genomics, Intellectual disability, Human genetics and NAA15 falls within the category of Genetics. His Genomics research is multidisciplinary, incorporating perspectives in Translational research, Human genome, Computational biology and Candidate gene.

The concepts of his Candidate gene study are interwoven with issues in Indel, Annotation, Molecular Sequence Annotation, INDEL Mutation and DNA sequencing. His work deals with themes such as Missense mutation, Contig, Allele and Bioinformatics, which intersect with Exome sequencing. Gholson J. Lyon has included themes like Clinical psychology, Attention deficit hyperactivity disorder, Tics and Genetic architecture in his Tourette syndrome study.

Between 2015 and 2021, his most popular works were:

  • Analysis of shared heritability in common disorders of the brain (726 citations)
  • The Human Phenotype Ontology in 2017 (471 citations)
  • Long-read sequencing and de novo assembly of a Chinese genome (176 citations)

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

  • Gene
  • Genetics
  • Mutation

Gholson J. Lyon mainly investigates Genetics, Tourette syndrome, Computational biology, Genome-wide association study and Attention deficit hyperactivity disorder. His work in Exome sequencing, Missense mutation, Shotgun sequencing, Reference genome and Sequence assembly is related to Genetics. His research in Exome sequencing is mostly concerned with Cancer genome sequencing.

His work carried out in the field of Tourette syndrome brings together such families of science as Tics, Proband and Copy-number variation. His studies deal with areas such as Indel, Human genome, Sequencing data and Genomics as well as Computational biology. Gholson J. Lyon interconnects Annotation, INDEL Mutation, DNA sequencing and Candidate gene in the investigation of issues within Genomics.

Best Publications

  • Analysis of shared heritability in common disorders of the brain

    Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters

  • The Human Phenotype Ontology in 2017

    Sebastian Köhler;Nicole A. Vasilevsky;Mark Engelstad;Erin D. Foster

  • Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome

    Matthew E. Hirschtritt;Paul C. Lee;David L. Pauls;Yves Dion

  • Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

    L C Papadopoulou;C M Sue;M M Davidson;K Tanji

  • Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

    Jason O'Rawe;Jason O'Rawe;Tao Jiang;Guangqing Sun;Yiyang Wu;Yiyang Wu

  • Peptide signaling in Staphylococcus aureus and other Gram-positive bacteria.

    Gholson J. Lyon;Richard P. Novick

  • Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

    Josephine Elia;Joseph T. Glessner;Kai Wang;Nagahide Takahashi

  • An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.

    Catherine A. Brownstein;Alan H. Beggs;Nils Homer;Barry Merriman

  • Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

    Dongmei Yu;Jae Hoon Sul;Fotis Tsetsos;Muhammad S Nawaz

  • Rational design of a global inhibitor of the virulence response in Staphylococcus aureus, based in part on localization of the site of inhibition to the receptor-histidine kinase, AgrC

    Gholson J. Lyon;Patricia Mayville;Tom W. Muir;Richard P. Novick

  • Exfoliatin-producing strains define a fourth agr specificity group in Staphylococcus aureus.

    S. Jarraud;G. J. Lyon;G. J. Lyon;A. M. S. Figueiredo;G. Lina

  • SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data

    Zhi-Jian Wei;Wei-wei Wang;Pingzhao Hu;Gholson J Lyon

  • Long-read sequencing and de novo assembly of a Chinese genome

    Lingling Shi;Lingling Shi;Yunfei Guo;Chengliang Dong;John Huddleston

  • Using VAAST to Identify an X-Linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

    Alan F. Rope;Kai Wang;Rune Evjenth;Jinchuan Xing

  • Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age-onset cataract formation and disruption of the lens.

    Darren T. Gilmour;Gholson J. Lyon;Mark B.L. Carlton;Joshua R. Sanes

  • Key determinants of receptor activation in the agr autoinducing peptides of Staphylococcus aureus.

    Gholson J. Lyon;Jesse S. Wright;Tom W. Muir;Richard P. Novick

  • Accurate de novo and transmitted indel detection in exome-capture data using microassembly

    Giuseppe Narzisi;Jason A O'Rawe;Ivan Iossifov;Han Fang

  • Genome-wide association study of Tourette's syndrome

    J. M. Scharf;J. M. Scharf;D. Yu;C. A. Mathews;B. M. Neale;B. M. Neale

  • Reducing INDEL calling errors in whole genome and exome sequencing data

    Han Fang;Yiyang Wu;Giuseppe Narzisi;Jason A ORawe;Jason A ORawe

  • Chemical Signaling among Bacteria and Its Inhibition

    Gholson J Lyon;Tom W Muir

Frequent Co-Authors

Danielle C. Cath
Danielle C. Cath Utrecht University
Robert A. King
Robert A. King Yale University
Hakon Hakonarson
Hakon Hakonarson Children's Hospital of Philadelphia
Benjamin M. Neale
Benjamin M. Neale Harvard University
William M. McMahon
William M. McMahon University of Utah
David L. Pauls
David L. Pauls Harvard University
Nelson B. Freimer
Nelson B. Freimer University of California, Los Angeles
Cathy L. Barr
Cathy L. Barr University Health Network
Mary M. Robertson
Mary M. Robertson University College London
Guy A. Rouleau
Guy A. Rouleau Montreal Neurological Institute and Hospital

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