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Results: 1 to 20 of 129

Related Citations for PubMed (Select 24592275)

1.

Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk.

Willis JA, Mukherjee S, Orlow I, Viale A, Offit K, Kurtz RC, Olson SH, Klein RJ.

Front Genet. 2014 Feb 13;5:29. doi: 10.3389/fgene.2014.00029. eCollection 2014.

2.

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.

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.

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.

Talseth-Palmer BA, Holliday EG, Evans TJ, McEvoy M, Attia J, Grice DM, Masson AL, Meldrum C, Spigelman A, Scott RJ.

BMC Med Genomics. 2013 Mar 26;6:10. doi: 10.1186/1755-8794-6-10.

5.

Germline copy number variation and ovarian cancer survival.

Fridley BL, Chalise P, Tsai YY, Sun Z, Vierkant RA, Larson MC, Cunningham JM, Iversen ES, Fenstermacher D, Barnholtz-Sloan J, Asmann Y, Risch HA, Schildkraut JM, Phelan CM, Sutphen R, Sellers TA, Goode EL.

Front Genet. 2012 Aug 8;3:142. doi: 10.3389/fgene.2012.00142. eCollection 2012.

6.

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

Yang R, Chen B, Pfütze K, Buch S, Steinke V, Holinski-Feder E, Stöcker S, von Schönfels W, Becker T, Schackert HK, Royer-Pokora B, Kloor M, Schmiegel WH, Büttner R, Engel C, Lascorz Puertolas J, Försti A, Kunkel N, Bugert P, Schreiber S, Krawczak M, Schafmayer C, Propping P, Hampe J, Hemminki K, Burwinkel B.

Carcinogenesis. 2014 Feb;35(2):315-23. doi: 10.1093/carcin/bgt344. Epub 2013 Oct 14.

7.

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
8.

Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests.

Lin CF, Naj AC, Wang LS.

Curr Protoc Hum Genet. 2013 Oct 18;79:Unit 1.27.. doi: 10.1002/0471142905.hg0127s79.

9.

A genome-wide CNV association study on panic disorder in a Japanese population.

Kawamura Y, Otowa T, Koike A, Sugaya N, Yoshida E, Yasuda S, Inoue K, Takei K, Konishi Y, Tanii H, Shimada T, Tochigi M, Kakiuchi C, Umekage T, Liu X, Nishida N, Tokunaga K, Kuwano R, Okazaki Y, Kaiya H, Sasaki T.

J Hum Genet. 2011 Dec;56(12):852-6. doi: 10.1038/jhg.2011.117. Epub 2011 Oct 20.

PMID:
22011818
10.

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.

Jarick I, Volckmar AL, Pütter C, Pechlivanis S, Nguyen TT, Dauvermann MR, Beck S, Albayrak Ö, Scherag S, Gilsbach S, Cichon S, Hoffmann P, Degenhardt F, Nöthen MM, Schreiber S, Wichmann HE, Jöckel KH, Heinrich J, Tiesler CM, Faraone SV, Walitza S, Sinzig J, Freitag C, Meyer J, Herpertz-Dahlmann B, Lehmkuhl G, Renner TJ, Warnke A, Romanos M, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J, Scherag A, Hinney A.

Mol Psychiatry. 2014 Jan;19(1):115-21. doi: 10.1038/mp.2012.161. Epub 2012 Nov 20.

11.

Endometriosis is associated with rare copy number variants.

Chettier R, Ward K, Albertsen HM.

PLoS One. 2014 Aug 1;9(8):e103968. doi: 10.1371/journal.pone.0103968. eCollection 2014.

12.

Identification of germline genomic copy number variation in familial pancreatic cancer.

Al-Sukhni W, Joe S, Lionel AC, Zwingerman N, Zogopoulos G, Marshall CR, Borgida A, Holter S, Gropper A, Moore S, Bondy M, Klein AP, Petersen GM, Rabe KG, Schwartz AG, Syngal S, Scherer SW, Gallinger S.

Hum Genet. 2012 Sep;131(9):1481-94. doi: 10.1007/s00439-012-1183-1. Epub 2012 Jun 5.

13.

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.

14.

Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.

Blauw HM, Veldink JH, van Es MA, van Vught PW, Saris CG, van der Zwaag B, Franke L, Burbach JP, Wokke JH, Ophoff RA, van den Berg LH.

Lancet Neurol. 2008 Apr;7(4):319-26. doi: 10.1016/S1474-4422(08)70048-6. Epub 2008 Mar 3.

PMID:
18313986
15.

Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array.

Molin AM, Berglund J, Webster MT, Lindblad-Toh K.

BMC Genomics. 2014 Mar 19;15:210. doi: 10.1186/1471-2164-15-210.

16.

A gender-specific association of CNV at 6p21.3 with NPC susceptibility.

Tse KP, Su WH, Yang ML, Cheng HY, Tsang NM, Chang KP, Hao SP, Yao Shugart Y, Chang YS.

Hum Mol Genet. 2011 Jul 15;20(14):2889-96. doi: 10.1093/hmg/ddr191. Epub 2011 May 2.

17.

Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study.

Yang TL, Guo Y, Shen H, Li J, Glessner JT, Qiu C, Deng FY, Tian Q, Yu P, Liu YZ, Liu YJ, Hakonarson H, Grant SF, Deng HW.

J Clin Endocrinol Metab. 2013 Jan;98(1):E191-5. doi: 10.1210/jc.2012-2751. Epub 2012 Nov 21.

18.

The effect of algorithms on copy number variant detection.

Tsuang DW, Millard SP, Ely B, Chi P, Wang K, Raskind WH, Kim S, Brkanac Z, Yu CE.

PLoS One. 2010 Dec 30;5(12):e14456. doi: 10.1371/journal.pone.0014456.

19.

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.

Jarick I, Vogel CI, Scherag S, Schäfer H, Hebebrand J, Hinney A, Scherag A.

Hum Mol Genet. 2011 Feb 15;20(4):840-52. doi: 10.1093/hmg/ddq518. Epub 2010 Dec 2.

20.

Genome-wide association study of copy number variations (CNVs) with opioid dependence.

Li D, Zhao H, Kranzler HR, Li MD, Jensen KP, Zayats T, Farrer LA, Gelernter J.

Neuropsychopharmacology. 2015 Mar;40(4):1016-26. doi: 10.1038/npp.2014.290. Epub 2014 Sep 27.

PMID:
25345593
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