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Lars Feuk
Lars Feuk
Email verificata su igp.uu.se
Titolo
Citata da
Citata da
Anno
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
50152006
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
34162004
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
25872010
Structural variation in the human genome
L Feuk, AR Carson, SW Scherer
Nature Reviews Genetics 7 (2), 85-97, 2006
24332006
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
21562007
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
20542010
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
19422008
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, A Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
15312007
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
10862014
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
10582006
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls
Wellcome Trust Case Control Consortium
Nature 464 (7289), 713, 2010
8672010
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
4492009
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
4382011
Challenges and standards in integrating surveys of structural variation
SW Scherer, C Lee, E Birney, DM Altshuler, EE Eichler, NP Carter, ...
Nature genetics 39 (7), S7-S15, 2007
4362007
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), 1-14, 2010
3352010
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
3352006
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
3212011
Copy-number variation in control population cohorts
D Pinto, C Marshall, L Feuk, SW Scherer
Human molecular genetics 16 (R2), R168-R173, 2007
2702007
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
2422001
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
2412006
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