World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
55
Citations
36224
World Ranking
3530
National Ranking
45

Lars Feuk 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 Lars Feuk 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: 121 publications — 16th percentile

16% of scientists in this discipline score the same or lower.

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

Lars Feuk 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 Lars Feuk 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

Lars Feuk is affiliated with Uppsala University in Sweden and has contributed extensively to the field of Biochemistry, Genetics, and Molecular Biology. Their research spans various subfields, including Molecular Biology, Genetics, Cancer Research, Public Health, Environmental and Occupational Health, and Insect Science.

Their work covers several main topics, such as:

  • Genomic variations and chromosomal abnormalities
  • Cancer Genomics and Diagnostics
  • Epigenetics and DNA Methylation
  • CRISPR and Genetic Engineering
  • RNA modifications and cancer
  • Genomics and Rare Diseases
  • Genomics and Phylogenetic Studies

Lars Feuk has authored multiple papers, with notable publications including:

  • "CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations" (2022, Nature Communications)
  • "Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity" (2020, Genome Biology)
  • "Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts" (2021, Scientific Reports)
  • "DLG4-related synaptopathy: a new rare brain disorder" (2021, Genetics in Medicine)
  • "Long-read whole-genome analysis of human single cells" (2023, Nature Communications)

Frequent coauthors collaborating with Lars Feuk include:

  • Adam Ameur
  • Ignas Bunikis
  • Jessica Nordlund
  • Anna Lindstrand
  • Jesper Eisfeldt

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

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Scientific Reports
  • Nature Communications
  • Genes
  • International Journal of Molecular Sciences

Best Publications

  • Global variation in copy number in the human genome

    Richard Redon;Shumpei Ishikawa;Karen R. Fitch;Lars Feuk

  • Detection of large-scale variation in the human genome.

    A John Iafrate;Lars Feuk;Miguel N Rivera;Miguel N Rivera;Marc L Listewnik

  • Consensus Statement : Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

    David T. Miller;Margaret P. Adam;Margaret P. Adam;Swaroop Aradhya;Leslie G. Biesecker

  • Structural variation in the human genome

    Lars Feuk;Andrew R. Carson;Stephen W. Scherer

  • The Diploid Genome Sequence of an Individual Human

    Samuel Levy;Granger Sutton;Pauline C Ng;Lars Feuk

  • Origins and functional impact of copy number variation in the human genome

    Donald F. Conrad;Dalila Pinto;Richard Redon;Richard Redon;Lars Feuk;Lars Feuk

  • Structural variation of chromosomes in autism spectrum disorder.

    Christian R. Marshall;Abdul Noor;John B. Vincent;Anath C. Lionel

  • Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts

  • The Database of Genomic Variants: a curated collection of structural variation in the human genome

    Jeffrey R. MacDonald;Robert Ziman;Ryan K. C. Yuen;Lars Feuk

  • Copy number variation: New insights in genome diversity

    Jennifer L. Freeman;George H. Perry;Lars Feuk;Richard Redon

  • Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

    Nick Craddock;Matthew E. Hurles;Niall Cardin;Richard D. Pearson

  • Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma

    Paul A. Northcott;Yukiko Nakahara;Xiaochong Wu;Lars Feuk

  • Challenges and standards in integrating surveys of structural variation.

    Stephen W Scherer;Charles Lee;Ewan Birney;David M Altshuler

  • Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

    Dalila Pinto;Katayoon Darvishi;Xinghua Shi;Diana Rajan

  • Towards a comprehensive structural variation map of an individual human genome

    Andy W Pang;Andy W Pang;Jeffrey R MacDonald;Dalila Pinto;John Wei

  • Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain

    Adam Ameur;Ammar Zaghlool;Jonatan Halvardson;Anna Wetterbom

  • Structural variants: changing the landscape of chromosomes and design of disease studies

    Lars Feuk;Christian R. Marshall;Richard F. Wintle;Stephen W. Scherer

  • Copy-number variation in control population cohorts

    Dalila Pinto;Christian Marshall;Christian Marshall;Lars Feuk;Lars Feuk;Stephen W. Scherer;Stephen W. Scherer

  • Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome

    J Zhang;L Feuk;G E Duggan;R Khaja

  • Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids

    Adam Ameur;Stefan Enroth;Åsa Johansson;Ghazal Zaboli

Frequent Co-Authors

Stephen W. Scherer
Stephen W. Scherer University of Toronto
Charles Lee
Charles Lee The Jackson Laboratory
Ulf Gyllensten
Ulf Gyllensten Uppsala University
Christian R. Marshall
Christian R. Marshall University of Toronto
Nigel P. Carter
Nigel P. Carter Wellcome Sanger Institute
Matthew E. Hurles
Matthew E. Hurles Wellcome Sanger Institute
Anthony J. Brookes
Anthony J. Brookes University of Leicester
Richard Redon
Richard Redon University of Nantes
Dalila Pinto
Dalila Pinto Icahn School of Medicine at Mount Sinai
John B. Vincent
John B. Vincent Centre for Addiction and Mental Health

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