Similar articles for PMID: 16651370

Year	Number of Results
1974	2
1981	1
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2010	17
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2012	8
2013	6
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2018	4
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2023	2
2024	0

1

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.

2

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.

3

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES. Kloth JN, et al. BMC Genomics. 2007 Feb 20;8:53. doi: 10.1186/1471-2164-8-53. BMC Genomics. 2007. PMID: 17311676 Free PMC article.

4

Emerging themes and new challenges in defining the role of structural variation in human disease.

Sharp AJ. Sharp AJ. Hum Mutat. 2009 Feb;30(2):135-44. doi: 10.1002/humu.20843. Hum Mutat. 2009. PMID: 18837009 Review.

5

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.

Lee C, Iafrate AJ, Brothman AR. Lee C, et al. Nat Genet. 2007 Jul;39(7 Suppl):S48-54. doi: 10.1038/ng2092. Nat Genet. 2007. PMID: 17597782 Review.

6

Identification of disease genes by whole genome CGH arrays.

Vissers LE, Veltman JA, van Kessel AG, Brunner HG. Vissers LE, et al. Hum Mol Genet. 2005 Oct 15;14 Spec No. 2:R215-23. doi: 10.1093/hmg/ddi268. Hum Mol Genet. 2005. PMID: 16244320 Review.

7

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.

Bruno DL, Ganesamoorthy D, Schoumans J, Bankier A, Coman D, Delatycki M, Gardner RJ, Hunter M, James PA, Kannu P, McGillivray G, Pachter N, Peters H, Rieubland C, Savarirayan R, Scheffer IE, Sheffield L, Tan T, White SM, Yeung A, Bowman Z, Ngo C, Choy KW, Cacheux V, Wong L, Amor DJ, Slater HR. Bruno DL, et al. J Med Genet. 2009 Feb;46(2):123-31. doi: 10.1136/jmg.2008.062604. Epub 2008 Nov 17. J Med Genet. 2009. PMID: 19015223

8

Pharmacogenetics: technologies to detect copy number variations.

Dhawan D, Padh H. Dhawan D, et al. Curr Opin Mol Ther. 2009 Dec;11(6):670-80. Curr Opin Mol Ther. 2009. PMID: 20072944 Review.

9

[Structural variation in the human genome contributes to variation of traits].

Barøy T, Misceo D, Frengen E. Barøy T, et al. Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1951-5. Tidsskr Nor Laegeforen. 2008. PMID: 18787571 Free article. Review. Norwegian.

10

The emerging role of structural variations in common disorders: initial findings and discovery challenges.

Armengol L, Rabionet R, Estivill X. Armengol L, et al. Cytogenet Genome Res. 2008;123(1-4):108-17. doi: 10.1159/000184698. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287145 Review.

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