Feuk L - Search Results

1

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome.

Shlien A, Tabori U, Marshall CR, Pienkowska M, Feuk L, Novokmet A, Nanda S, Druker H, Scherer SW, Malkin D. Shlien A, et al. Among authors: feuk l. Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11264-9. doi: 10.1073/pnas.0802970105. Epub 2008 Aug 6. Proc Natl Acad Sci U S A. 2008. PMID: 18685109 Free PMC article.

2

Long-read whole-genome analysis of human single cells.

Hård J, Mold JE, Eisfeldt J, Tellgren-Roth C, Häggqvist S, Bunikis I, Contreras-Lopez O, Chin CS, Nordlund J, Rubin CJ, Feuk L, Michaëlsson J, Ameur A. Hård J, et al. Among authors: feuk l. Nat Commun. 2023 Aug 24;14(1):5164. doi: 10.1038/s41467-023-40898-3. Nat Commun. 2023. PMID: 37620373 Free PMC article.

3

Detection of large-scale variation in the human genome.

Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, Scherer SW, Lee C. Iafrate AJ, et al. Among authors: feuk l. Nat Genet. 2004 Sep;36(9):949-51. doi: 10.1038/ng1416. Epub 2004 Aug 1. Nat Genet. 2004. PMID: 15286789 Free article.

4

Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies.

Feuk L, MacDonald JR, Tang T, Carson AR, Li M, Rao G, Khaja R, Scherer SW. Feuk L, et al. PLoS Genet. 2005 Oct;1(4):e56. doi: 10.1371/journal.pgen.0010056. Epub 2005 Oct 28. PLoS Genet. 2005. PMID: 16254605 Free PMC article.

5

Structural variation in the human genome.

Feuk L, Carson AR, Scherer SW. Feuk L, et al. Nat Rev Genet. 2006 Feb;7(2):85-97. doi: 10.1038/nrg1767. Nat Rev Genet. 2006. PMID: 16418744 Review.

6

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW. Zeesman S, et al. Among authors: feuk l. Am J Med Genet A. 2006 Mar 1;140(5):509-14. doi: 10.1002/ajmg.a.31110. Am J Med Genet A. 2006. PMID: 16470794

7

Structural variants: changing the landscape of chromosomes and design of disease studies.

Feuk L, Marshall CR, Wintle RF, Scherer SW. Feuk L, et al. Hum Mol Genet. 2006 Apr 15;15 Spec No 1:R57-66. doi: 10.1093/hmg/ddl057. Hum Mol Genet. 2006. PMID: 16651370 Review.

8

Copy number variation: new insights in genome diversity.

Freeman JL, Perry GH, Feuk L, Redon R, McCarroll SA, Altshuler DM, Aburatani H, Jones KW, Tyler-Smith C, Hurles ME, Carter NP, Scherer SW, Lee C. Freeman JL, et al. Among authors: feuk l. Genome Res. 2006 Aug;16(8):949-61. doi: 10.1101/gr.3677206. Epub 2006 Jun 29. Genome Res. 2006. PMID: 16809666 Free article. Review.

9

Strategies for the detection of copy number and other structural variants in the human genome.

Carson AR, Feuk L, Mohammed M, Scherer SW. Carson AR, et al. Among authors: feuk l. Hum Genomics. 2006 Jun;2(6):403-14. doi: 10.1186/1479-7364-2-6-403. Hum Genomics. 2006. PMID: 16848978 Free PMC article. Review.

10

Frequent appearance of novel protein-coding sequences by frameshift translation.

Okamura K, Feuk L, Marquès-Bonet T, Navarro A, Scherer SW. Okamura K, et al. Among authors: feuk l. Genomics. 2006 Dec;88(6):690-697. doi: 10.1016/j.ygeno.2006.06.009. Epub 2006 Aug 4. Genomics. 2006. PMID: 16890400 Free article.

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