World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

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

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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