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Results: 1 to 20 of 245

Related Citations for PubMed (Select 22493684)

1.

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.

2.

Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.

Valsesia A, Stevenson BJ, Waterworth D, Mooser V, Vollenweider P, Waeber G, Jongeneel CV, Beckmann JS, Kutalik Z, Bergmann S.

BMC Genomics. 2012 Jun 15;13:241. doi: 10.1186/1471-2164-13-241.

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.

4.

Genome-wide algorithm for detecting CNV associations with diseases.

Xu Y, Peng B, Fu Y, Amos CI.

BMC Bioinformatics. 2011 Aug 9;12:331. doi: 10.1186/1471-2105-12-331.

5.

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.

Eckel-Passow JE, Atkinson EJ, Maharjan S, Kardia SL, de Andrade M.

BMC Bioinformatics. 2011 May 31;12:220. doi: 10.1186/1471-2105-12-220.

6.

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.

Bae JS, Cheong HS, Park BL, Kim LH, Park TJ, Kim JY, Pasaje CF, Lee JS, Cui T, Inoue I, Shin HD.

J Hum Genet. 2010 Nov;55(11):726-30. doi: 10.1038/jhg.2010.97. Epub 2010 Aug 12.

PMID:
20703242
7.

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
8.

Genome-wide analysis of copy number variations reveals that aging processes influence body fat distribution in Korea Associated Resource (KARE) cohorts.

Lee BY, Shin DH, Cho S, Seo KS, Kim H.

Hum Genet. 2012 Nov;131(11):1795-804. doi: 10.1007/s00439-012-1203-1. Epub 2012 Jul 24.

PMID:
22825314
9.

No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort.

Bagshaw AT, Horwood LJ, Liu Y, Fergusson DM, Sullivan PF, Kennedy MA.

PLoS One. 2013;8(1):e55208. doi: 10.1371/journal.pone.0055208. Epub 2013 Jan 30.

10.

Analysis of copy number variations in the sheep genome using 50K SNP BeadChip array.

Liu J, Zhang L, Xu L, Ren H, Lu J, Zhang X, Zhang S, Zhou X, Wei C, Zhao F, Du L.

BMC Genomics. 2013 Apr 8;14:229. doi: 10.1186/1471-2164-14-229.

11.

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.

12.

Identification of copy number variation hotspots in human populations.

Fu W, Zhang F, Wang Y, Gu X, Jin L.

Am J Hum Genet. 2010 Oct 8;87(4):494-504. doi: 10.1016/j.ajhg.2010.09.006.

13.

Structural architecture of SNP effects on complex traits.

Gamazon ER, Cox NJ, Davis LK.

Am J Hum Genet. 2014 Nov 6;95(5):477-89. doi: 10.1016/j.ajhg.2014.09.009. Epub 2014 Oct 9.

PMID:
25307299
14.

Copy number variation accuracy in genome-wide association studies.

Lin P, Hartz SM, Wang JC, Krueger RF, Foroud TM, Edenberg HJ, Nurnberger JI Jr, Brooks AI, Tischfield JA, Almasy L, Webb BT, Hesselbrock VM, Porjesz B, Goate AM, Bierut LJ, Rice JP; COGA Collaborators; COGEND Collaborators; GENEVA Investigators.

Hum Hered. 2011;71(3):141-7. doi: 10.1159/000324683. Epub 2011 Jul 20.

15.

The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.

Wain LV, Pedroso I, Landers JE, Breen G, Shaw CE, Leigh PN, Brown RH, Tobin MD, Al-Chalabi A.

PLoS One. 2009 Dec 4;4(12):e8175. doi: 10.1371/journal.pone.0008175.

16.

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.

17.

A genome wide association study between copy number variation (CNV) and human height in Chinese population.

Li X, Tan L, Liu X, Lei S, Yang T, Chen X, Zhang F, Fang Y, Guo Y, Zhang L, Yan H, Pan F, Zhang Z, Peng Y, Zhou Q, He L, Zhu X, Cheng J, Zhang L, Liu Y, Tian Q, Deng H.

J Genet Genomics. 2010 Dec;37(12):779-85. doi: 10.1016/S1673-8527(09)60095-3.

PMID:
21193156
18.

Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.

Bae JS, Cheong HS, Chun JY, Park TJ, Kim JO, Kim EM, Park M, Kim DJ, Lee EJ, Kim EK, Lee JY, Shin HD.

Ophthalmology. 2010 Jul;117(7):1306-12.e4. doi: 10.1016/j.ophtha.2009.11.021. Epub 2010 Mar 3.

PMID:
20202685
19.

COKGEN: a software for the identification of rare copy number variation from SNP microarrays.

Yavaş G, Koyutürk M, Ozsoyoğlu M, Gould MP, Laframboise T.

Pac Symp Biocomput. 2010:371-82.

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.

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