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Items: 1 to 20 of 94

1.

Large-scale copy number polymorphism in the human genome.

Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, Månér S, Massa H, Walker M, Chi M, Navin N, Lucito R, Healy J, Hicks J, Ye K, Reiner A, Gilliam TC, Trask B, Patterson N, Zetterberg A, Wigler M.

Science. 2004 Jul 23;305(5683):525-8.

2.

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.

de Bustos C, Díaz de Ståhl T, Piotrowski A, Mantripragada KK, Buckley PG, Darai E, Hansson CM, Grigelionis G, Menzel U, Dumanski JP.

Genomics. 2006 Aug;88(2):152-62. Epub 2006 May 18.

3.

Copy-number polymorphisms: mining the tip of an iceberg.

Buckley PG, Mantripragada KK, Piotrowski A, Diaz de Ståhl T, Dumanski JP.

Trends Genet. 2005 Jun;21(6):315-7. Review.

PMID:
15922827
4.

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
5.

Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster.

Emerson JJ, Cardoso-Moreira M, Borevitz JO, Long M.

Science. 2008 Jun 20;320(5883):1629-31. doi: 10.1126/science.1158078. Epub 2008 Jun 5.

6.

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.

7.

Genome-wide analysis of DNA copy-number changes using cDNA microarrays.

Pollack JR, Perou CM, Alizadeh AA, Eisen MB, Pergamenschikov A, Williams CF, Jeffrey SS, Botstein D, Brown PO.

Nat Genet. 1999 Sep;23(1):41-6.

PMID:
10471496
8.

Copy-number variants in patients with a strong family history of pancreatic cancer.

Lucito R, Suresh S, Walter K, Pandey A, Lakshmi B, Krasnitz A, Sebat J, Wigler M, Klein AP, Brune K, Palmisano E, Maitra A, Goggins M, Hruban RH.

Cancer Biol Ther. 2007 Oct;6(10):1592-9. Epub 2007 Jul 12.

PMID:
17912030
9.

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.

10.

Gene expression profiling and gene copy-number changes in malignant mesothelioma cell lines.

Zanazzi C, Hersmus R, Veltman IM, Gillis AJ, van Drunen E, Beverloo HB, Hegmans JP, Verweij M, Lambrecht BN, Oosterhuis JW, Looijenga LH.

Genes Chromosomes Cancer. 2007 Oct;46(10):895-908.

PMID:
17620293
11.

Segmental duplications and copy-number variation in the human genome.

Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, Vallente RU, Pertz LM, Clark RA, Schwartz S, Segraves R, Oseroff VV, Albertson DG, Pinkel D, Eichler EE.

Am J Hum Genet. 2005 Jul;77(1):78-88. Epub 2005 May 25.

12.
13.

Genome wide gene amplifications and deletions in Plasmodium falciparum.

Ribacke U, Mok BW, Wirta V, Normark J, Lundeberg J, Kironde F, Egwang TG, Nilsson P, Wahlgren M.

Mol Biochem Parasitol. 2007 Sep;155(1):33-44. Epub 2007 May 18.

PMID:
17599553
14.

High-resolution copy number arrays in cancer and the problem of normal genome copy number variation.

Gorringe KL, Campbell IG.

Genes Chromosomes Cancer. 2008 Nov;47(11):933-8. doi: 10.1002/gcc.20595.

PMID:
18663746
15.

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.

16.

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.

Sharp AJ, Hansen S, Selzer RR, Cheng Z, Regan R, Hurst JA, Stewart H, Price SM, Blair E, Hennekam RC, Fitzpatrick CA, Segraves R, Richmond TA, Guiver C, Albertson DG, Pinkel D, Eis PS, Schwartz S, Knight SJ, Eichler EE.

Nat Genet. 2006 Sep;38(9):1038-42. Epub 2006 Aug 13.

PMID:
16906162
17.

[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.

18.

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.

BMC Genomics. 2007 Feb 20;8:53.

19.
20.

Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci.

Buckley PG, Jarbo C, Menzel U, Mathiesen T, Scott C, Gregory SG, Langford CF, Dumanski JP.

Cancer Res. 2005 Apr 1;65(7):2653-61.

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