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Items: 1 to 20 of 53

1.

Characterization of Copy Number Variation's Potential Role in Marek's Disease.

Xu L, He Y, Ding Y, Sun G, Carrillo JA, Li Y, Ghaly MM, Ma L, Zhang H, Liu GE, Song J.

Int J Mol Sci. 2017 May 9;18(5). pii: E1020. doi: 10.3390/ijms18051020.

2.

Kernel-Based Aggregation of Marker-Level Genetic Association Tests Involving Copy-Number Variation.

Li Y, Breheny P.

Microarrays (Basel). 2013 Sep 4;2(3):265-83. doi: 10.3390/microarrays2030265.

3.

A novel copy number variants kernel association test with application to autism spectrum disorders studies.

Zhan X, Girirajan S, Zhao N, Wu MC, Ghosh D.

Bioinformatics. 2016 Dec 1;32(23):3603-3610. Epub 2016 Aug 6.

PMID:
27497442
4.

Copy number variations and stroke.

Colaianni V, Mazzei R, Cavallaro S.

Neurol Sci. 2016 Dec;37(12):1895-1904. Epub 2016 Jul 8. Review.

5.

Differential frequency of NKG2C/KLRC2 deletion in distinct African populations and susceptibility to Trachoma: a new method for imputation of KLRC2 genotypes from SNP genotyping data.

Goncalves A, Makalo P, Joof H, Burr S, Ramadhani A, Massae P, Malisa A, Mtuy T, Derrick T, Last AR, Nabicassa M, Cassama E, Houghton J, Palmer CD, Pickering H, Burton MJ, Mabey DC, Bailey RL, Goodier MR, Holland MJ, Roberts CH.

Hum Genet. 2016 Aug;135(8):939-51. doi: 10.1007/s00439-016-1694-2. Epub 2016 Jun 16.

6.

Genetic Variations in Vesicoureteral Reflux Sequelae.

Hains DS, Schwaderer AL.

Pathogens. 2016 Feb 2;5(1). pii: E14. doi: 10.3390/pathogens5010014. Review.

7.

Statistical analysis for genome-wide association study.

Zeng P, Zhao Y, Qian C, Zhang L, Zhang R, Gou J, Liu J, Liu L, Chen F.

J Biomed Res. 2015 Jul;29(4):285-97. doi: 10.7555/JBR.29.20140007. Epub 2014 Nov 30. Review.

8.

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.

9.

Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.

Cooper NJ, Shtir CJ, Smyth DJ, Guo H, Swafford AD, Zanda M, Hurles ME, Walker NM, Plagnol V, Cooper JD, Howson JM, Burren OS, Onengut-Gumuscu S, Rich SS, Todd JA.

Hum Mol Genet. 2015 Mar 15;24(6):1774-90. doi: 10.1093/hmg/ddu581. Epub 2014 Nov 25.

10.

Genome wide CNV analysis reveals additional variants associated with milk production traits in Holsteins.

Xu L, Cole JB, Bickhart DM, Hou Y, Song J, VanRaden PM, Sonstegard TS, Van Tassell CP, Liu GE.

BMC Genomics. 2014 Aug 15;15:683. doi: 10.1186/1471-2164-15-683.

11.

The genetic basis of music ability.

Tan YT, McPherson GE, Peretz I, Berkovic SF, Wilson SJ.

Front Psychol. 2014 Jun 27;5:658. doi: 10.3389/fpsyg.2014.00658. eCollection 2014. Review.

12.

Ordered subset analysis of copy number variation association with age at onset of Alzheimer's disease.

Szigeti K, Kellermayer B, Lentini JM, Trummer B, Lal D, Doody RS, Yan L, Liu S, Ma C; Texas Alzheimer Research and Care Consortium.

J Alzheimers Dis. 2014;41(4):1063-71. doi: 10.3233/JAD-132693.

13.

Using high-density DNA methylation arrays to profile copy number alterations.

Feber A, Guilhamon P, Lechner M, Fenton T, Wilson GA, Thirlwell C, Morris TJ, Flanagan AM, Teschendorff AE, Kelly JD, Beck S.

Genome Biol. 2014 Feb 3;15(2):R30. doi: 10.1186/gb-2014-15-2-r30.

14.

Urinary bladder cancer susceptibility markers. What do we know about functional mechanisms?

Dudek AM, Grotenhuis AJ, Vermeulen SH, Kiemeney LA, Verhaegh GW.

Int J Mol Sci. 2013 Jun 10;14(6):12346-66. doi: 10.3390/ijms140612346. Review.

15.

The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation.

Valsesia A, Macé A, Jacquemont S, Beckmann JS, Kutalik Z.

Front Genet. 2013 May 30;4:92. doi: 10.3389/fgene.2013.00092. eCollection 2013.

16.

Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis.

Wu CC, Shete S, Jo EJ, Xu Y, Lu EY, Chen WV, Amos CI.

Hum Mol Genet. 2013 Mar 15;22(6):1249-61. doi: 10.1093/hmg/dds512. Epub 2012 Dec 6.

17.

Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease.

Szigeti K, Lal D, Li Y, Doody RS, Wilhelmsen K, Yan L, Liu S, Ma C; Texas Alzheimer Research and Care Consortium.

J Alzheimers Dis. 2013;33(2):517-23. doi: 10.3233/JAD-2012-121285.

18.

Human complex trait genetics: lifting the lid of the genomics toolbox - from pathways to prediction.

Rowe SJ, Tenesa A.

Curr Genomics. 2012 May;13(3):213-24. doi: 10.2174/138920212800543101.

19.

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.

20.

The rhoptry proteins ROP18 and ROP5 mediate Toxoplasma gondii evasion of the murine, but not the human, interferon-gamma response.

Niedelman W, Gold DA, Rosowski EE, Sprokholt JK, Lim D, Farid Arenas A, Melo MB, Spooner E, Yaffe MB, Saeij JP.

PLoS Pathog. 2012;8(6):e1002784. doi: 10.1371/journal.ppat.1002784. Epub 2012 Jun 28.

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