Lars Feuk
Lars Feuk
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Cited by
Cited by
Global variation in copy number in the human genome
R Redon, S Ishikawa, KR Fitch, L Feuk, GH Perry, TD Andrews, H Fiegler, ...
nature 444 (7118), 444-454, 2006
Detection of large-scale variation in the human genome
AJ Iafrate, L Feuk, MN Rivera, ML Listewnik, PK Donahoe, Y Qi, ...
Nature genetics 36 (9), 949-951, 2004
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
DT Miller, MP Adam, S Aradhya, LG Biesecker, AR Brothman, NP Carter, ...
The American Journal of Human Genetics 86 (5), 749-764, 2010
Structural variation in the human genome
L Feuk, AR Carson, SW Scherer
Nature Reviews Genetics 7 (2), 85-97, 2006
The diploid genome sequence of an individual human
S Levy, G Sutton, PC Ng, L Feuk, AL Halpern, BP Walenz, N Axelrod, ...
PLoS biology 5 (10), e254, 2007
Origins and functional impact of copy number variation in the human genome
DF Conrad, D Pinto, R Redon, L Feuk, O Gokcumen, Y Zhang, J Aerts, ...
Nature 464 (7289), 704-712, 2010
Structural variation of chromosomes in autism spectrum disorder
CR Marshall, A Noor, JB Vincent, AC Lionel, L Feuk, J Skaug, M Shago, ...
The American Journal of Human Genetics 82 (2), 477-488, 2008
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
The Database of Genomic Variants: a curated collection of structural variation in the human genome
JR MacDonald, R Ziman, RKC Yuen, L Feuk, SW Scherer
Nucleic acids research 42 (D1), D986-D992, 2014
Copy number variation: new insights in genome diversity
JL Freeman, GH Perry, L Feuk, R Redon, SA McCarroll, DM Altshuler, ...
Genome research 16 (8), 949-961, 2006
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nature 464 (7289), 713-720, 2010
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma
PA Northcott, Y Nakahara, X Wu, L Feuk, DW Ellison, S Croul, S Mack, ...
Nature genetics 41 (4), 465-472, 2009
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
D Pinto, K Darvishi, X Shi, D Rajan, D Rigler, T Fitzgerald, AC Lionel, ...
Nature biotechnology 29 (6), 512-520, 2011
Challenges and standards in integrating surveys of structural variation
SW Scherer, C Lee, E Birney, DM Altshuler, EE Eichler, NP Carter, ...
Nature genetics 39 (Suppl 7), S7-S15, 2007
Towards a comprehensive structural variation map of an individual human genome
AW Pang, JR MacDonald, D Pinto, J Wei, MA Rafiq, DF Conrad, H Park, ...
Genome biology 11, 1-14, 2010
Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain
A Ameur, A Zaghlool, J Halvardson, A Wetterbom, U Gyllensten, ...
Nature structural & molecular biology 18 (12), 1435-1440, 2011
Structural variants: changing the landscape of chromosomes and design of disease studies
L Feuk, CR Marshall, RF Wintle, SW Scherer
Human molecular genetics 15 (suppl_1), R57-R66, 2006
Copy-number variation in control population cohorts
D Pinto, C Marshall, L Feuk, SW Scherer
Human molecular genetics 16 (R2), R168-R173, 2007
Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids
A Ameur, S Enroth, Johansson, G Zaboli, W Igl, ACV Johansson, ...
The American Journal of Human Genetics 90 (5), 809-820, 2012
SNP association studies in Alzheimer's disease highlight problems for complex disease analysis
T Emahazion, L Feuk, M Jobs, SL Sawyer, D Fredman, D St Clair, ...
TRENDS in Genetics 17 (7), 407-413, 2001
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