Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 39

2.

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
3.

Extending genome-wide association studies to copy-number variation.

McCarroll SA.

Hum Mol Genet. 2008 Oct 15;17(R2):R135-42. doi: 10.1093/hmg/ddn282. Review.

PMID:
18852202
4.

[Genome-wide detection of loss of heterozygosity and copy number variation in a human lung large cell carcinoma cell line by affymetrix single-nucleotide polymorphism array 500K.].

Hu B, Chen J, Liu H, Wu H, Wu Z, Wang Y, Bai Y, Li Y, Zhou Q.

Zhongguo Fei Ai Za Zhi. 2008 Jun 20;11(3):327-32. doi: 10.3779/j.issn.1009-3419.2008.03.017. Chinese.

5.

Detection and characterization of copy number variation in autism spectrum disorder.

Marshall CR, Scherer SW.

Methods Mol Biol. 2012;838:115-35. doi: 10.1007/978-1-61779-507-7_5. Review.

PMID:
22228009
6.

Implications of gene copy-number variation in health and diseases.

Almal SH, Padh H.

J Hum Genet. 2012 Jan;57(1):6-13. doi: 10.1038/jhg.2011.108. Epub 2011 Sep 29. Review.

PMID:
21956041
7.

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.

8.

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.

Weiss LA.

Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Review.

PMID:
19895225
9.

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics.

Gai X, Perin JC, Murphy K, O'Hara R, D'arcy M, Wenocur A, Xie HM, Rappaport EF, Shaikh TH, White PS.

BMC Bioinformatics. 2010 Feb 4;11:74. doi: 10.1186/1471-2105-11-74.

10.

A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals.

Teo SM, Ku CS, Naidoo N, Hall P, Chia KS, Salim A, Pawitan Y.

J Hum Genet. 2011 Jul;56(7):524-33. doi: 10.1038/jhg.2011.52. Epub 2011 Jun 2.

PMID:
21633363
11.

What a difference copy number variation makes.

Kehrer-Sawatzki H.

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

PMID:
17373652
12.

Cardiac hypertrophy and hypertension.

Dunn FG.

Blood Press Suppl. 1995;2:17-21. Review.

PMID:
7582068
13.

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
14.

Copy Number Variation Detection via High-Density SNP Genotyping.

Wang K, Bucan M.

CSH Protoc. 2008 Jun 1;2008:pdb.top46. doi: 10.1101/pdb.top46.

PMID:
21356857
15.

Variation of CNV distribution in five different ethnic populations.

White SJ, Vissers LE, Geurts van Kessel A, de Menezes RX, Kalay E, Lehesjoki AE, Giordano PC, van de Vosse E, Breuning MH, Brunner HG, den Dunnen JT, Veltman JA.

Cytogenet Genome Res. 2007;118(1):19-30.

PMID:
17901696
16.

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
17.

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.

18.

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
19.

[Prognostic implications of left ventricular hypertrophy in arterial hypertension].

Kannel WB.

Arch Mal Coeur Vaiss. 1990 Dec;83 Spec No 4:11-21. French.

PMID:
2150470
20.

Supplemental Content

Support Center