| 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 | 5508 | 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 | 3614 | 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 | 3252 | 2010 |
| Structural variation in the human genome L Feuk, AR Carson, SW Scherer Nature Reviews Genetics 7 (2), 85-97, 2006 | 2790 | 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 | 2338 | 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 | 2295 | 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 | 2194 | 2008 |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1671 | 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 | 1446 | 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 | 1184 | 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 | 943 | 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 | 501 | 2009 |
| 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 | 487 | 2007 |
| 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 | 485 | 2011 |
| 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 | 406 | 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 | 389 | 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 | 374 | 2006 |
| Copy-number variation in control population cohorts D Pinto, C Marshall, L Feuk, SW Scherer Human molecular genetics 16 (R2), R168-R173, 2007 | 297 | 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, Å Johansson, G Zaboli, W Igl, ACV Johansson, ... The American Journal of Human Genetics 90 (5), 809-820, 2012 | 269 | 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 | 258 | 2001 |
