Articles with public access mandates - Lars FeukLearn more
Not available anywhere: 3
Welander Distal Myopathy Caused by an Ancient Founder Mutation in TIA1 Associated with Perturbed Splicing
J Klar, M Sobol, A Melberg, K Mäbert, A Ameur, ACV Johansson, L Feuk, ...
Human mutation 34 (4), 572-577, 2013
Mandates: Swedish Research Council
Characterization of copy number‐stable regions in the human genome
ACV Johansson, L Feuk
Human Mutation 32 (8), 947-955, 2011
Mandates: Swedish Research Council
Copy number variation in the autism genome
L Feuk
Expert Opinion on Medical Diagnostics 2 (4), 417-428, 2008
Mandates: Canadian Institutes of Health Research
Available somewhere: 73
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
Mandates: Genome Canada
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Structural variation in the human genome
L Feuk, AR Carson, SW Scherer
Nature Reviews Genetics 7 (2), 85-97, 2006
Mandates: Genome Canada
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
Mandates: Genome Canada
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
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
Mandates: Canadian Institutes of Health Research, Genome Canada
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
Mandates: Genome Canada, German Research Foundation
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
Mandates: Canadian Institutes of Health Research, Genome Canada
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
Mandates: Genome Canada
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
Mandates: Versus Arthritis, UK, British Heart Foundation
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
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
Mandates: Genome Canada
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
Mandates: Canadian Institutes of Health Research, Genome Canada
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
Mandates: Genome Canada
Copy-number variation in control population cohorts
D Pinto, C Marshall, L Feuk, SW Scherer
Human molecular genetics 16 (R2), R168-R173, 2007
Mandates: Genome Canada
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, Å Johansson, G Zaboli, W Igl, ACV Johansson, ...
The American Journal of Human Genetics 90 (5), 809-820, 2012
Mandates: Swedish Research Council
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