Similar articles for PMID: 17296953

Year	Number of Results
1998	1
2000	1
2001	1
2003	1
2004	4
2005	4
2006	7
2007	23
2008	5
2009	7
2010	6
2011	1
2012	2
2017	1
2023	1
2024	0

1

Copy-number variations add a new layer of complexity in the human genome.

Hegele RA. Hegele RA. CMAJ. 2007 Feb 13;176(4):441-2. doi: 10.1503/cmaj.061689. CMAJ. 2007. PMID: 17296953 Free PMC article. No abstract available.

2

Gene expression profiling and gene copy-number changes in malignant mesothelioma cell lines.

Zanazzi C, Hersmus R, Veltman IM, Gillis AJ, van Drunen E, Beverloo HB, Hegmans JP, Verweij M, Lambrecht BN, Oosterhuis JW, Looijenga LH. Zanazzi C, et al. Genes Chromosomes Cancer. 2007 Oct;46(10):895-908. doi: 10.1002/gcc.20475. Genes Chromosomes Cancer. 2007. PMID: 17620293

3

Accurate and reliable high-throughput detection of copy number variation in the human genome.

Fiegler H, Redon R, Andrews D, Scott C, Andrews R, Carder C, Clark R, Dovey O, Ellis P, Feuk L, French L, Hunt P, Kalaitzopoulos D, Larkin J, Montgomery L, Perry GH, Plumb BW, Porter K, Rigby RE, Rigler D, Valsesia A, Langford C, Humphray SJ, Scherer SW, Lee C, Hurles ME, Carter NP. Fiegler H, et al. Genome Res. 2006 Dec;16(12):1566-74. doi: 10.1101/gr.5630906. Epub 2006 Nov 22. Genome Res. 2006. PMID: 17122085 Free PMC article.

4

Integrated analysis of expression and genome alteration reveals putative amplified target genes in esophageal cancer.

Sugimoto T, Arai M, Shimada H, Hata A, Seki N. Sugimoto T, et al. Oncol Rep. 2007 Aug;18(2):465-72. Oncol Rep. 2007. PMID: 17611672

5

Optimal design of oligonucleotide microarrays for measurement of DNA copy-number.

Sharp AJ, Itsara A, Cheng Z, Alkan C, Schwartz S, Eichler EE. Sharp AJ, et al. Hum Mol Genet. 2007 Nov 15;16(22):2770-9. doi: 10.1093/hmg/ddm234. Epub 2007 Aug 28. Hum Mol Genet. 2007. PMID: 17725982

6

Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes.

Lo KC, Rossi MR, LaDuca J, Hicks DG, Turpaz Y, Hawthorn L, Cowell JK. Lo KC, et al. Genes Chromosomes Cancer. 2007 Oct;46(10):875-94. doi: 10.1002/gcc.20474. Genes Chromosomes Cancer. 2007. PMID: 17620294

7

[Detection for subtype-specific genomic/genetic alterations in diffuse large B-cell lymphoma (DLBCL)].

Tagawa H. Tagawa H. Rinsho Ketsueki. 2008 Feb;49(2):73-81. Rinsho Ketsueki. 2008. PMID: 18341036 Review. Japanese. No abstract available.

8

Integrated high-resolution genome-wide analysis of gene dosage and gene expression in human brain tumors.

Juric D, Bredel C, Sikic BI, Bredel M. Juric D, et al. Methods Mol Biol. 2007;377:187-202. doi: 10.1007/978-1-59745-390-5_12. Methods Mol Biol. 2007. PMID: 17634618 Review.

9

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.

de Bustos C, Díaz de Ståhl T, Piotrowski A, Mantripragada KK, Buckley PG, Darai E, Hansson CM, Grigelionis G, Menzel U, Dumanski JP. de Bustos C, et al. Genomics. 2006 Aug;88(2):152-62. doi: 10.1016/j.ygeno.2006.03.016. Epub 2006 May 18. Genomics. 2006. PMID: 16713171 Free article.

10

Enrichment of super-sized resequencing targets from the human genome.

Olson M. Olson M. Nat Methods. 2007 Nov;4(11):891-2. doi: 10.1038/nmeth1107-891. Nat Methods. 2007. PMID: 17971778 No abstract available.

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