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Lars Feuk | Researchclopedia

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Lars Feuk

Uppsala University ORCID

173

Works

30,601

Citations

51

h-index

92

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Genomics and Rare Diseases Genomics and Phylogenetic Studies

Affiliations

Uppsala University2009–2025

J. Craig Venter Institute2007–2007

National Food Administration2025–2025

St. Jude Children's Research Hospital2007–2007

Uppsala University Hospital2012–2012

Top Works

Global variation in copy number in the human genome

Richard Redon,Shumpei Ishikawa,et al.

20064,350 citations

Chromosomal and Genetic Variations

Genetics and Neurodevelopmental Disorders

Detection of large-scale variation in the human genome

A. John Iafrate,Lars Feuk,et al.

20042,910 citations

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,et al.

20102,855 citations

Structural variation in the human genome

Lars Feuk,Andrew R. Carson,et al.

20062,063 citations

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

Donald F. Conrad,Dalila Pinto,et al.

20092,045 citations

Structural Variation of Chromosomes in Autism Spectrum Disorder

Christian R. Marshall,Abdul Noor,et al.

20081,833 citations

The Diploid Genome Sequence of an Individual Human

Samuel Lévy,Granger Sutton,et al.

20071,817 citations

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

Jeffrey R. MacDonald,Robert Ziman,et al.

20131,398 citations

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Péter Szatmári,Ping G. Tepper,et al.

20071,388 citations