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Results: 1 to 20 of 229

1.

Copy number variants, diseases and gene expression.

Henrichsen CN, Chaignat E, Reymond A.

Hum Mol Genet. 2009 Apr 15;18(R1):R1-8. doi: 10.1093/hmg/ddp011. Review.

PMID:
19297395
[PubMed - indexed for MEDLINE]
Free Article
2.

What a difference copy number variation makes.

Kehrer-Sawatzki H.

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

PMID:
17373652
[PubMed - indexed for MEDLINE]
3.

Segmental copy number variation shapes tissue transcriptomes.

Henrichsen CN, Vinckenbosch N, Zöllner S, Chaignat E, Pradervand S, Schütz F, Ruedi M, Kaessmann H, Reymond A.

Nat Genet. 2009 Apr;41(4):424-9. doi: 10.1038/ng.345. Epub 2009 Mar 8.

PMID:
19270705
[PubMed - indexed for MEDLINE]
4.

A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.

Lin CH, Lin YC, Wu JY, Pan WH, Chen YT, Fann CS.

Genomics. 2009 Oct;94(4):241-6. doi: 10.1016/j.ygeno.2009.06.004. Epub 2009 Jun 25.

PMID:
19559783
[PubMed - indexed for MEDLINE]
Free Article
5.

Expression divergence and copy number variation in the human genome.

Auer H.

Cytogenet Genome Res. 2008;123(1-4):278-82. doi: 10.1159/000184718. Epub 2009 Mar 11.

PMID:
19287165
[PubMed - indexed for MEDLINE]
6.

The fine-scale and complex architecture of human copy-number variation.

Perry GH, Ben-Dor A, Tsalenko A, Sampas N, Rodriguez-Revenga L, Tran CW, Scheffer A, Steinfeld I, Tsang P, Yamada NA, Park HS, Kim JI, Seo JS, Yakhini Z, Laderman S, Bruhn L, Lee C.

Am J Hum Genet. 2008 Mar;82(3):685-95. doi: 10.1016/j.ajhg.2007.12.010. Epub 2008 Jan 24.

PMID:
18304495
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Extensive copy-number variation of the human olfactory receptor gene family.

Young JM, Endicott RM, Parghi SS, Walker M, Kidd JM, Trask BJ.

Am J Hum Genet. 2008 Aug;83(2):228-42. doi: 10.1016/j.ajhg.2008.07.005.

PMID:
18674749
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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

Armengol L, Rabionet R, Estivill X.

Cytogenet Genome Res. 2008;123(1-4):108-17. doi: 10.1159/000184698. Epub 2009 Mar 11. Review.

PMID:
19287145
[PubMed - indexed for MEDLINE]
9.

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

Marioni JC, Thorne NP, Valsesia A, Fitzgerald T, Redon R, Fiegler H, Andrews TD, Stranger BE, Lynch AG, Dermitzakis ET, Carter NP, Tavaré S, Hurles ME.

Genome Biol. 2007;8(10):R228.

PMID:
17961237
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.

Beckmann JS, Estivill X, Antonarakis SE.

Nat Rev Genet. 2007 Aug;8(8):639-46. Review.

PMID:
17637735
[PubMed - indexed for MEDLINE]
11.

Methods and strategies for analyzing copy number variation using DNA microarrays.

Carter NP.

Nat Genet. 2007 Jul;39(7 Suppl):S16-21. Review.

PMID:
17597776
[PubMed - indexed for MEDLINE]
Free PMC Article
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
[PubMed - indexed for MEDLINE]
13.

Copy-number variation in control population cohorts.

Pinto D, Marshall C, Feuk L, Scherer SW.

Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R168-73. Review. Erratum in: Hum Mol Genet. 2008 Feb 1;17(3):166-7.

PMID:
17911159
[PubMed - indexed for MEDLINE]
Free Article
14.

Copy number variations (CNVs) identified in Korean individuals.

Kang TW, Jeon YJ, Jang E, Kim HJ, Kim JH, Park JL, Lee S, Kim YS, Kim JY, Kim SY.

BMC Genomics. 2008 Oct 18;9:492. doi: 10.1186/1471-2164-9-492.

PMID:
18928558
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.

Lee AS, Gutiérrez-Arcelus M, Perry GH, Vallender EJ, Johnson WE, Miller GM, Korbel JO, Lee C.

Hum Mol Genet. 2008 Apr 15;17(8):1127-36. doi: 10.1093/hmg/ddn002. Epub 2008 Jan 7.

PMID:
18180252
[PubMed - indexed for MEDLINE]
Free Article
16.

A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan.

Lin CH, Li LH, Ho SF, Chuang TP, Wu JY, Chen YT, Fann CS.

BMC Genet. 2008 Dec 24;9:92. doi: 10.1186/1471-2156-9-92.

PMID:
19108714
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Relating CNVs to transcriptome data at fine resolution: assessment of the effect of variant size, type, and overlap with functional regions.

Schlattl A, Anders S, Waszak SM, Huber W, Korbel JO.

Genome Res. 2011 Dec;21(12):2004-13. doi: 10.1101/gr.122614.111. Epub 2011 Aug 23.

PMID:
21862627
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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.

PMID:
17289997
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Copy-number variation and association studies of human disease.

McCarroll SA, Altshuler DM.

Nat Genet. 2007 Jul;39(7 Suppl):S37-42. Review.

PMID:
17597780
[PubMed - indexed for MEDLINE]
20.

Copy number alterations and copy number variation in cancer: close encounters of the bad kind.

Speleman F, Kumps C, Buysse K, Poppe B, Menten B, De Preter K.

Cytogenet Genome Res. 2008;123(1-4):176-82. doi: 10.1159/000184706. Epub 2009 Mar 11. Review.

PMID:
19287153
[PubMed - indexed for MEDLINE]

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