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Items: 1 to 20 of 133

1.

Structural variation in the human genome.

Feuk L, Carson AR, Scherer SW.

Nat Rev Genet. 2006 Feb;7(2):85-97. Review.

PMID:
16418744
2.

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

Barøy T, Misceo D, Frengen E.

Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1951-5. Review. Norwegian.

3.

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

Feuk L, Marshall CR, Wintle RF, Scherer SW.

Hum Mol Genet. 2006 Apr 15;15 Spec No 1:R57-66. Review.

4.

[Structural variation in the human genome].

He YS, Zhang W, Yang ZQ.

Yi Chuan. 2009 Aug;31(8):771-8. Review. Chinese.

PMID:
19689936
5.

Side effects of genome structural changes.

Reymond A, Henrichsen CN, Harewood L, Merla G.

Curr Opin Genet Dev. 2007 Oct;17(5):381-6. Epub 2007 Oct 24. Review.

PMID:
17913489
6.

Common deletions and SNPs are in linkage disequilibrium in the human genome.

Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA.

Nat Genet. 2006 Jan;38(1):82-5. Epub 2005 Dec 4.

PMID:
16327809
7.

Pharmacogenetics: technologies to detect copy number variations.

Dhawan D, Padh H.

Curr Opin Mol Ther. 2009 Dec;11(6):670-80. Review.

PMID:
20072944
8.

Fine-scale structural variation of the human genome.

Tuzun E, Sharp AJ, Bailey JA, Kaul R, Morrison VA, Pertz LM, Haugen E, Hayden H, Albertson D, Pinkel D, Olson MV, Eichler EE.

Nat Genet. 2005 Jul;37(7):727-32. Epub 2005 May 15.

PMID:
15895083
9.

Detection of copy number variation using SNP genotyping.

Cooper GM, Mefford HC.

Methods Mol Biol. 2011;767:243-52. doi: 10.1007/978-1-61779-201-4_18.

PMID:
21822880
10.

Progress in the detection of human genome structural variations.

WU X, XIAO H.

Sci China C Life Sci. 2009 Jun;52(6):560-7. doi: 10.1007/s11427-009-0078-4. Epub 2009 Jun 26. Review.

PMID:
19557334
11.

Human genome variation in health and in neuropsychiatric disorders.

Buretić-Tomljanović A, Tomljanović D.

Psychiatr Danub. 2009 Dec;21(4):562-9. Review.

12.

[Copy-number variation: a new pattern of structural diversity in genome].

Wu ZJ, Jin W.

Yi Chuan. 2009 Apr;31(4):339-47. Review. Chinese.

PMID:
19586885
13.

Structural variation in the human genome: the impact of copy number variants on clinical diagnosis.

Rodriguez-Revenga L, Mila M, Rosenberg C, Lamb A, Lee C.

Genet Med. 2007 Sep;9(9):600-6. Review.

PMID:
17873648
14.

SNP discovery and typing technologies for pharmacogenomics.

Twyman RM.

Curr Top Med Chem. 2004;4(13):1423-31. Review.

PMID:
15379655
15.

Mutational and selective effects on copy-number variants in the human genome.

Cooper GM, Nickerson DA, Eichler EE.

Nat Genet. 2007 Jul;39(7 Suppl):S22-9. Review.

PMID:
17597777
16.

Genome assembly comparison identifies structural variants in the human genome.

Khaja R, Zhang J, MacDonald JR, He Y, Joseph-George AM, Wei J, Rafiq MA, Qian C, Shago M, Pantano L, Aburatani H, Jones K, Redon R, Hurles M, Armengol L, Estivill X, Mural RJ, Lee C, Scherer SW, Feuk L.

Nat Genet. 2006 Dec;38(12):1413-8. Epub 2006 Nov 22.

17.

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

Carson AR, Feuk L, Mohammed M, Scherer SW.

Hum Genomics. 2006 Jun;2(6):403-14. Review.

18.

What a difference copy number variation makes.

Kehrer-Sawatzki H.

Bioessays. 2007 Apr;29(4):311-3.

PMID:
17373652
19.

Genetic variation analysis for biomedical researchers: a primer.

Barnes MR.

Methods Mol Biol. 2010;628:1-20. doi: 10.1007/978-1-60327-367-1_1. Review.

PMID:
20238073
20.

Relative impact of nucleotide and copy number variation on gene expression phenotypes.

Stranger BE, Forrest MS, Dunning M, Ingle CE, Beazley C, Thorne N, Redon R, Bird CP, de Grassi A, Lee C, Tyler-Smith C, Carter N, Scherer SW, Tavaré S, Deloukas P, Hurles ME, Dermitzakis ET.

Science. 2007 Feb 9;315(5813):848-53.

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