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Results: 1 to 20 of 289

1.

Copy number polymorphisms and anticancer pharmacogenomics.

Gamazon ER, Huang RS, Dolan ME, Cox NJ.

Genome Biol. 2011;12(5):R46. doi: 10.1186/gb-2011-12-5-r46. Epub 2011 May 25.

PMID:
21609475
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.

Gamazon ER, Nicolae DL, Cox NJ.

PLoS Genet. 2011 Feb 3;7(2):e1001292. doi: 10.1371/journal.pgen.1001292.

PMID:
21304891
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach.

Kalari KR, Hebbring SJ, Chai HS, Li L, Kocher JP, Wang L, Weinshilboum RM.

BMC Genomics. 2010 Jun 4;11:357. doi: 10.1186/1471-2164-11-357.

PMID:
20525348
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Chemotherapeutic-induced apoptosis: a phenotype for pharmacogenomics studies.

Wen Y, Gorsic LK, Wheeler HE, Ziliak DM, Huang RS, Dolan ME.

Pharmacogenet Genomics. 2011 Aug;21(8):476-88. doi: 10.1097/FPC.0b013e3283481967.

PMID:
21642893
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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
6.

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
7.

Population differences in platinum toxicity as a means to identify novel genetic susceptibility variants.

O'Donnell PH, Gamazon E, Zhang W, Stark AL, Kistner-Griffin EO, Stephanie Huang R, Eileen Dolan M.

Pharmacogenet Genomics. 2010 May;20(5):327-37. doi: 10.1097/FPC.0b013e3283396c4e.

PMID:
20393316
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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
9.

Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity.

Waszak SM, Hasin Y, Zichner T, Olender T, Keydar I, Khen M, Stütz AM, Schlattl A, Lancet D, Korbel JO.

PLoS Comput Biol. 2010 Nov 11;6(11):e1000988. doi: 10.1371/journal.pcbi.1000988.

PMID:
21085617
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits.

Chen C, Qiao R, Wei R, Guo Y, Ai H, Ma J, Ren J, Huang L.

BMC Genomics. 2012 Dec 27;13:733. doi: 10.1186/1471-2164-13-733.

PMID:
23270433
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.

Ionita-Laza I, Perry GH, Raby BA, Klanderman B, Lee C, Laird NM, Weiss ST, Lange C.

Genet Epidemiol. 2008 Apr;32(3):273-84. doi: 10.1002/gepi.20302.

PMID:
18228561
[PubMed - indexed for MEDLINE]
12.

Whole genome survey of copy number variation in the spontaneously hypertensive rat: relationship to quantitative trait loci, gene expression, and blood pressure.

Charchar FJ, Kaiser M, Bingham AJ, Fotinatos N, Ahmady F, Tomaszewski M, Samani NJ.

Hypertension. 2010 May;55(5):1231-8. doi: 10.1161/HYPERTENSIONAHA.109.141663. Epub 2010 Mar 15. Erratum in: Hypertension. 2010 Jun;55(6):e28.

PMID:
20231529
[PubMed - indexed for MEDLINE]
Free Article
13.

Genetic association studies of copy-number variation: should assignment of copy number states precede testing?

Breheny P, Chalise P, Batzler A, Wang L, Fridley BL.

PLoS One. 2012;7(4):e34262. doi: 10.1371/journal.pone.0034262. Epub 2012 Apr 6.

PMID:
22493684
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity.

Huang RS, Duan S, Bleibel WK, Kistner EO, Zhang W, Clark TA, Chen TX, Schweitzer AC, Blume JE, Cox NJ, Dolan ME.

Proc Natl Acad Sci U S A. 2007 Jun 5;104(23):9758-63. Epub 2007 May 30.

PMID:
17537913
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Origins and functional impact of copy number variation in the human genome.

Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, Macarthur DG, Macdonald JR, Onyiah I, Pang AW, Robson S, Stirrups K, Valsesia A, Walter K, Wei J; Wellcome Trust Case Control Consortium, Tyler-Smith C, Carter NP, Lee C, Scherer SW, Hurles ME.

Nature. 2010 Apr 1;464(7289):704-12. doi: 10.1038/nature08516. Epub 2009 Oct 7.

PMID:
19812545
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

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
17.

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
[PubMed - indexed for MEDLINE]
18.

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.

Wellcome Trust Case Control Consortium, Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, Robson S, Vukcevic D, Barnes C, Conrad DF, Giannoulatou E, Holmes C, Marchini JL, Stirrups K, Tobin MD, Wain LV, Yau C, Aerts J, Ahmad T, Andrews TD, Arbury H, Attwood A, Auton A, Ball SG, Balmforth AJ, Barrett JC, Barroso I, Barton A, Bennett AJ, Bhaskar S, Blaszczyk K, Bowes J, Brand OJ, Braund PS, Bredin F, Breen G, Brown MJ, Bruce IN, Bull J, Burren OS, Burton J, Byrnes J, Caesar S, Clee CM, Coffey AJ, Connell JM, Cooper JD, Dominiczak AF, Downes K, Drummond HE, Dudakia D, Dunham A, Ebbs B, Eccles D, Edkins S, Edwards C, Elliot A, Emery P, Evans DM, Evans G, Eyre S, Farmer A, Ferrier IN, Feuk L, Fitzgerald T, Flynn E, Forbes A, Forty L, Franklyn JA, Freathy RM, Gibbs P, Gilbert P, Gokumen O, Gordon-Smith K, Gray E, Green E, Groves CJ, Grozeva D, Gwilliam R, Hall A, Hammond N, Hardy M, Harrison P, Hassanali N, Hebaishi H, Hines S, Hinks A, Hitman GA, Hocking L, Howard E, Howard P, Howson JM, Hughes D, Hunt S, Isaacs JD, Jain M, Jewell DP, Johnson T, Jolley JD, Jones IR, Jones LA, Kirov G, Langford CF, Lango-Allen H, Lathrop GM, Lee J, Lee KL, Lees C, Lewis K, Lindgren CM, Maisuria-Armer M, Maller J, Mansfield J, Martin P, Massey DC, McArdle WL, McGuffin P, McLay KE, Mentzer A, Mimmack ML, Morgan AE, Morris AP, Mowat C, Myers S, Newman W, Nimmo ER, O'Donovan MC, Onipinla A, Onyiah I, Ovington NR, Owen MJ, Palin K, Parnell K, Pernet D, Perry JR, Phillips A, Pinto D, Prescott NJ, Prokopenko I, Quail MA, Rafelt S, Rayner NW, Redon R, Reid DM, Renwick, Ring SM, Robertson N, Russell E, St Clair D, Sambrook JG, Sanderson JD, Schuilenburg H, Scott CE, Scott R, Seal S, Shaw-Hawkins S, Shields BM, Simmonds MJ, Smyth DJ, Somaskantharajah E, Spanova K, Steer S, Stephens J, Stevens HE, Stone MA, Su Z, Symmons DP, Thompson JR, Thomson W, Travers ME, Turnbull C, Valsesia A, Walker M, Walker NM, Wallace C, Warren-Perry M, Watkins NA, Webster J, Weedon MN, Wilson AG, Woodburn M, Wordsworth BP, Young AH, Zeggini E, Carter NP, Frayling TM, Lee C, McVean G, Munroe PB, Palotie A, Sawcer SJ, Scherer SW, Strachan DP, Tyler-Smith C, Brown MA, Burton PR, Caulfield MJ, Compston A, Farrall M, Gough SC, Hall AS, Hattersley AT, Hill AV, Mathew CG, Pembrey M, Satsangi J, Stratton MR, Worthington J, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand W, Parkes M, Rahman N, Todd JA, Samani NJ, Donnelly P.

Nature. 2010 Apr 1;464(7289):713-20. doi: 10.1038/nature08979.

PMID:
20360734
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

CONAN: copy number variation analysis software for genome-wide association studies.

Forer L, Schönherr S, Weissensteiner H, Haider F, Kluckner T, Gieger C, Wichmann HE, Specht G, Kronenberg F, Kloss-Brandstätter A.

BMC Bioinformatics. 2010 Jun 14;11:318. doi: 10.1186/1471-2105-11-318.

PMID:
20546565
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Novel association strategy with copy number variation for identifying new risk Loci of human diseases.

Chen X, Li X, Wang P, Liu Y, Zhang Z, Zhao G, Xu H, Zhu J, Qin X, Chen S, Hu L, Kong X.

PLoS One. 2010 Aug 20;5(8):e12185. doi: 10.1371/journal.pone.0012185.

PMID:
20808825
[PubMed - indexed for MEDLINE]
Free PMC Article

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