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Results: 1 to 20 of 168

1.

Germ-line DNA copy number variation frequencies in a large North American population.

Zogopoulos G, Ha KC, Naqib F, Moore S, Kim H, Montpetit A, Robidoux F, Laflamme P, Cotterchio M, Greenwood C, Scherer SW, Zanke B, Hudson TJ, Bader GD, Gallinger S.

Hum Genet. 2007 Nov;122(3-4):345-53. Epub 2007 Jul 19.

PMID:
17638019
[PubMed - indexed for MEDLINE]
2.

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
3.

Copy number variation in African Americans.

McElroy JP, Nelson MR, Caillier SJ, Oksenberg JR.

BMC Genet. 2009 Mar 24;10:15. doi: 10.1186/1471-2156-10-15.

PMID:
19317893
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes.

Shen F, Huang J, Fitch KR, Truong VB, Kirby A, Chen W, Zhang J, Liu G, McCarroll SA, Jones KW, Shapero MH.

BMC Genet. 2008 Mar 28;9:27. doi: 10.1186/1471-2156-9-27.

PMID:
18373861
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array.

Hu N, Wang C, Hu Y, Yang HH, Kong LH, Lu N, Su H, Wang QH, Goldstein AM, Buetow KH, Emmert-Buck MR, Taylor PR, Lee MP.

BMC Genomics. 2006 Nov 29;7:299.

PMID:
17134496
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.

Li J, Yang T, Wang L, Yan H, Zhang Y, Guo Y, Pan F, Zhang Z, Peng Y, Zhou Q, He L, Zhu X, Deng H, Levy S, Papasian CJ, Drees BM, Hamilton JJ, Recker RR, Cheng J, Deng HW.

PLoS One. 2009 Nov 23;4(11):e7958. doi: 10.1371/journal.pone.0007958.

PMID:
19956714
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Global variation in copy number in the human genome.

Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, González JR, Gratacòs M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME.

Nature. 2006 Nov 23;444(7118):444-54.

PMID:
17122850
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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
9.

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
10.

Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia.

Braude I, Vukovic B, Prasad M, Marrano P, Turley S, Barber D, Zielenska M, Squire JA.

BMC Genomics. 2006 Jun 6;7:138.

PMID:
16756668
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Population structure in copy number variation and SNPs in the CCL4L chemokine gene.

Colobran R, Comas D, Faner R, Pedrosa E, Anglada R, Pujol-Borrell R, Bertranpetit J, Juan M.

Genes Immun. 2008 Jun;9(4):279-88. doi: 10.1038/gene.2008.15. Epub 2008 Mar 27.

PMID:
18368065
[PubMed - indexed for MEDLINE]
12.

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array.

Díaz de Ståhl T, Sandgren J, Piotrowski A, Nord H, Andersson R, Menzel U, Bogdan A, Thuresson AC, Poplawski A, von Tell D, Hansson CM, Elshafie AI, Elghazali G, Imreh S, Nordenskjöld M, Upadhyaya M, Komorowski J, Bruder CE, Dumanski JP.

Hum Mutat. 2008 Mar;29(3):398-408.

PMID:
18058796
[PubMed - indexed for MEDLINE]
13.

Towards a comprehensive structural variation map of an individual human genome.

Pang AW, MacDonald JR, Pinto D, Wei J, Rafiq MA, Conrad DF, Park H, Hurles ME, Lee C, Venter JC, Kirkness EF, Levy S, Feuk L, Scherer SW.

Genome Biol. 2010;11(5):R52. doi: 10.1186/gb-2010-11-5-r52. Epub 2010 May 19.

PMID:
20482838
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.

Baross A, Delaney AD, Li HI, Nayar T, Flibotte S, Qian H, Chan SY, Asano J, Ally A, Cao M, Birch P, Brown-John M, Fernandes N, Go A, Kennedy G, Langlois S, Eydoux P, Friedman JM, Marra MA.

BMC Bioinformatics. 2007 Oct 2;8:368.

PMID:
17910767
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population.

Bae JS, Cheong HS, Kim JO, Lee SO, Kim EM, Lee HW, Kim S, Kim JW, Cui T, Inoue I, Shin HD.

Biochem Biophys Res Commun. 2008 Sep 5;373(4):593-6. doi: 10.1016/j.bbrc.2008.06.083. Epub 2008 Jul 2.

PMID:
18601904
[PubMed - indexed for MEDLINE]
16.

[Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0].

Ma F, Wu FX, Li N, Liu Q, Yang W, Zhang X, Sun M.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):336-9. doi: 10.3760/cma.j.issn.1003-9406.2009.03.022. Chinese.

PMID:
19504452
[PubMed - indexed for MEDLINE]
17.

Analysis of genome-wide copy number variation in Irish and Dutch ALS populations.

Cronin S, Blauw HM, Veldink JH, van Es MA, Ophoff RA, Bradley DG, van den Berg LH, Hardiman O.

Hum Mol Genet. 2008 Nov 1;17(21):3392-8. doi: 10.1093/hmg/ddn233. Epub 2008 Aug 7.

PMID:
18689356
[PubMed - indexed for MEDLINE]
Free Article
18.

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.

Komura D, Shen F, Ishikawa S, Fitch KR, Chen W, Zhang J, Liu G, Ihara S, Nakamura H, Hurles ME, Lee C, Scherer SW, Jones KW, Shapero MH, Huang J, Aburatani H.

Genome Res. 2006 Dec;16(12):1575-84. Epub 2006 Nov 22.

PMID:
17122084
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis.

Yang TL, Chen XD, Guo Y, Lei SF, Wang JT, Zhou Q, Pan F, Chen Y, Zhang ZX, Dong SS, Xu XH, Yan H, Liu X, Qiu C, Zhu XZ, Chen T, Li M, Zhang H, Zhang L, Drees BM, Hamilton JJ, Papasian CJ, Recker RR, Song XP, Cheng J, Deng HW.

Am J Hum Genet. 2008 Dec;83(6):663-74. doi: 10.1016/j.ajhg.2008.10.006. Epub 2008 Nov 6.

PMID:
18992858
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Detection of genome-wide polymorphisms in the AT-rich Plasmodium falciparum genome using a high-density microarray.

Jiang H, Yi M, Mu J, Zhang L, Ivens A, Klimczak LJ, Huyen Y, Stephens RM, Su XZ.

BMC Genomics. 2008 Aug 25;9:398. doi: 10.1186/1471-2164-9-398.

PMID:
18724869
[PubMed - indexed for MEDLINE]
Free PMC Article
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