https://doi.org/10.1016/j.ajhg.2010.04.006
L
Lars Feuk
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Lars Feuk is an academic researcher from Uppsala University. The author has contributed to research in topics: Genomic variations and chromosomal abnormalities & Genomics and Rare Diseases & Genomics and Phylogenetic Studies. The author has an h-index of 51, co-authored 148 publications.
ORCID: 0000-0003-2355-2919Papers by this author
worksConsensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
2010 · The American Journal of Human Genetics · 2,835 citations
Structural variation in the human genome
2006 · Nature Reviews Genetics · 2,045 citations
https://doi.org/10.1038/nrg1767
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
2010 · Nature · 810 citations
https://doi.org/10.1038/nature08979
Towards a comprehensive structural variation map of an individual human genome
2010 · Genome biology · 355 citations
https://doi.org/10.1186/gb-2010-11-5-r52
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
2017 · European Journal of Human Genetics · 210 citations
https://doi.org/10.1038/ejhg.2017.130
CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations
2022 · Nature Communications · 175 citations
https://doi.org/10.1038/s41467-022-28244-5
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