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Items: 1 to 20 of 121

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.

Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity.

Shrine N, Tobin MD, Schurmann C, Soler Artigas M, Hui J, Lehtimäki T, Raitakari OT, Pennell CE, Ang QW, Strachan DP, Homuth G, Gläser S, Felix SB, Evans DM, Henderson J, Granell R, Palmer LJ, Huffman J, Hayward C, Scotland G, Malarstig A, Musk B, James AL; UK BiLEVE., Wain LV.

BMC Genet. 2016 Aug 11;17(1):116. doi: 10.1186/s12863-016-0423-0.

3.

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.

4.

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.

5.

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.

6.

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.

7.

A genome-wide assessment of rare copy number variants in colorectal cancer.

Li Z, Yu D, Gan M, Shan Q, Yin X, Tang S, Zhang S, Shi Y, Zhu Y, Lai M, Zhang D.

Oncotarget. 2015 Sep 22;6(28):26411-23. doi: 10.18632/oncotarget.4621.

8.

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.

9.

The association of copy number variation and percent mammographic density.

Atkinson EJ, Eckel-Passow JE, Wang A, Greenberg AJ, Scott CG, Pankratz VS, Purrington KN, Sellers TA, Rider DN, Heit JA, de Andrade M, Cunningham JM, Couch FJ, Vachon CM.

BMC Res Notes. 2015 Jul 8;8:297. doi: 10.1186/s13104-015-1212-y.

10.

Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism.

Wang Y, Li J, Kolon TF, Olivant Fisher A, Figueroa TE, BaniHani AH, Hagerty JA, Gonzalez R, Noh PH, Chiavacci RM, Harden KR, Abrams DJ, Stabley D, Kim CE, Sol-Church K, Hakonarson H, Devoto M, Barthold JS.

BMC Urol. 2016 Oct 21;16(1):62.

11.

Copy number variations in the genome of the Qatari population.

Fakhro KA, Yousri NA, Rodriguez-Flores JL, Robay A, Staudt MR, Agosto-Perez F, Salit J, Malek JA, Suhre K, Jayyousi A, Zirie M, Stadler D, Mezey JG, Crystal RG.

BMC Genomics. 2015 Oct 22;16:834. doi: 10.1186/s12864-015-1991-5.

12.

Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.

Sokolowski M, Wasserman J, Wasserman D.

PLoS One. 2016 Dec 28;11(12):e0168531. doi: 10.1371/journal.pone.0168531. eCollection 2016.

13.

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.

14.

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.

PMID:
24127187
15.

A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci.

Low JS, Chin YM, Mushiroda T, Kubo M, Govindasamy GK, Pua KC, Yap YY, Yap LF, Subramaniam SK, Ong CA, Tan TY, Khoo AS; Malaysian NPC Study Group., Ng CC.

PLoS One. 2016 Jan 5;11(1):e0145774. doi: 10.1371/journal.pone.0145774. eCollection 2016.

16.

Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases.

Moosmann J, Uebe S, Dittrich S, Rüffer A, Ekici AB, Toka O.

PLoS One. 2015 May 18;10(5):e0126873. doi: 10.1371/journal.pone.0126873. eCollection 2015.

17.

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
18.

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.

19.

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

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