Lars Feuk
Lars Feuk
Associate Professor, Uppsala University
Verified email at igp.uu.se
TitleCited byYear
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, 2006
44322006
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, 2004
31692004
Structural variation in the human genome
L Feuk, AR Carson, SW Scherer
Nature Reviews Genetics 7 (2), 85, 2006
20042006
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
19882010
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
19222007
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, 2010
17822010
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
16702008
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
13652007
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
8692006
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
N Craddock, ME Hurles, N Cardin, RD Pearson, V Plagnol, S Robson, ...
Nature 464 (7289), 713, 2010
7762010
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, 2013
6992013
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, 2009
3992009
Challenges and standards in integrating surveys of structural variation
SW Scherer, C Lee, E Birney, DM Altshuler, EE Eichler, NP Carter, ...
Nature genetics 39 (7s), S7-S15, 2007
3762007
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, 2011
3672011
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
2952006
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 (5), R52, 2010
2692010
Copy-number variation in control population cohorts
D Pinto, C Marshall, L Feuk, SW Scherer
Human molecular genetics 16 (R2), R168-R173, 2007
2612007
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, 2011
2362011
Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome
J Zhang, L Feuk, GE Duggan, R Khaja, SW Scherer
Cytogenetic and genome research 115 (3-4), 205-214, 2006
2352006
Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation
JA Prince, L Feuk, WM Howell, M Jobs, T Emahazion, K Blennow, ...
Genome research 11 (1), 152-162, 2001
2242001
The system can't perform the operation now. Try again later.
Articles 1–20