World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
69
Citations
20044
World Ranking
2334
National Ranking
1054

Ethan M. Lange 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 Ethan M. Lange 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: 239 publications — 63rd percentile

63% of scientists in this discipline score the same or lower.

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

Ethan M. Lange 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 Ethan M. Lange 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: 69 D-Index — 47th percentile

47% of scientists in this discipline score the same or lower.

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

Overview

Ethan M. Lange is affiliated with the University of Colorado Anschutz Medical Campus in the United States. Their research primarily spans the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with significant contributions in Genetics and Molecular Biology subfields.

Their scholarly work emphasizes several main topics including:

  • Genetic Associations and Epidemiology
  • Epigenetics and DNA Methylation
  • Birth, Development, and Health
  • Prostate Cancer Treatment and Research
  • Genetic and phenotypic traits in livestock
  • Genetic Mapping and Diversity in Plants and Animals
  • Adipokines, Inflammation, and Metabolic Diseases

Among their recent research papers are:

  • Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022, Nature Genetics)
  • Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease (2023, Nature Communications)
  • Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci (2021, Genome Medicine)
  • DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function (2021, Clinical Epigenetics)
  • Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study (2022, Journal of the American Heart Association)

Frequently publishing in venues such as UNC Libraries, bioRxiv (Cold Spring Harbor Laboratory), Nature Communications, Zenodo (CERN European Organization for Nuclear Research), and Circulation, their work appears consistently in both preprint and peer-reviewed journals.

Frequent collaborators in their research include:

  • Leslie A. Lange
  • Laura M. Raffield (31 co-authored papers)
  • Stephen S. Rich (25 co-authored papers)
  • Jerome I. Rotter (22 co-authored papers)

This body of work reflects a sustained focus on genetic and molecular mechanisms related to human health, with applications to cardiovascular, renal, and developmental biology. The scientist's contributions span epidemiological genetics and molecular studies aimed at understanding complex traits and disease associations across diverse populations.

Best Publications

  • REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

    Nilah M M. Ioannidis;Joseph H H. Rothstein;Joseph H H. Rothstein;Vikas Pejaver;Sumit Middha

  • Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

    Ron Do;Ron Do;Nathan O. Stitziel;Hong Hee Won;Hong Hee Won;Anders Berg Jørgensen

  • Inherited causes of clonal haematopoiesis in 97,691 whole genomes.

    Alexander G Bick;Joshua S Weinstock;Satish K Nandakumar;Satish K Nandakumar;Charles P Fulco;Charles P Fulco

  • Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

    Rosalind A. Eeles;Ali Amin Al Olama;Sara Benlloch;Edward J. Saunders

  • Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

    Rosalind A. Eeles;Zsofia Kote-Jarai;Ali Amin Al Olama;Graham G. Giles;Graham G. Giles

  • Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

    Jianfeng Xu;S. Lilly Zheng;Akira Komiya;Josyf C. Mychaleckyj

  • Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    Valérie Turcot;Yingchang Lu;Yingchang Lu;Heather M Highland;Heather M Highland;Claudia Schurmann

  • Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events.

    Leslie A. Lange;Christopher S. Carlson;Lucia A. Hindorff;Ethan M. Lange

  • Genetic modifiers of liver disease in cystic fibrosis.

    Jaclyn R. Bartlett;Kenneth J. Friedman;Simon C. Ling;Rhonda G. Pace

  • The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

    Soumitra Ghosh;Richard M. Watanabe;Timo T. Valle;Elizabeth R. Hauser

  • Prostate Cancer Susceptibility Locus on Chromosome 1q: A Confirmatory Study

    K.A. Cooney;J.D. McCarthy;E. Lange;L. Huang

  • Exploring the genetic basis of chronic periodontitis: a genome-wide association study

    Kimon Divaris;Keri L. Monda;Keri L. Monda;Kari E North;Andrew F Olshan

  • Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.

    Fred A. Wright;Lisa J. Strug;Vishal K. Doshi;Clayton W. Commander

  • Single-nucleotide polymorphisms in the C-reactive protein (CRP) gene promoter that affect transcription factor binding, alter transcriptional activity, and associate with differences in baseline serum CRP level

    A. J. Szalai;A. J. Szalai;J. Wu;E. M. Lange;M. A. McCrory

  • Randomized comparison of prophylactic and minimal residual disease-triggered imatinib after allogeneic stem cell transplantation for BCR-ABL1-positive acute lymphoblastic leukemia.

    Pfeifer H;Wassmann B;Bethge W;Dengler J

  • Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

    Leslie A Lange;Youna Hu;He Zhang;Chenyi Xue

  • HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)

    Jianfeng Xu;Ethan M. Lange;Ethan M. Lange;Lingyi Lu;Siqun L. Zheng

  • Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer

    Tasha R. Smith;Mark Steven Miller;Kurt Lohman;Ethan M. Lange

  • Rare and low-frequency coding variants alter human adult height

    Eirini Marouli;Mariaelisa Graff;Carolina Medina-Gomez;Ken Sin Lo

  • Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

    Jennifer Wessel;Audrey Y. Chu;Sara M. Willems;Shuai Wang

Frequent Co-Authors

Leslie A. Lange
Leslie A. Lange University of Colorado Anschutz Medical Campus
Alexander P. Reiner
Alexander P. Reiner University of Washington
James G. Wilson
James G. Wilson University of Mississippi Medical Center
Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
Kari E. North
Kari E. North University of North Carolina at Chapel Hill
Jianfeng Xu
Jianfeng Xu Arkansas State University
Karen L. Mohlke
Karen L. Mohlke University of North Carolina at Chapel Hill
William B. Isaacs
William B. Isaacs Johns Hopkins University
Graham G. Giles
Graham G. Giles University of Melbourne
Elaine A. Ostrander
Elaine A. Ostrander National Institutes of Health

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