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Items: 1 to 20 of 40

1.

Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study.

Wineinger NE, Patki A, Meyers KJ, Broeckel U, Gu CC, Rao DC, Devereux RB, Arnett DK, Tiwari HK.

BMC Med Genomics. 2011 Jan 11;4:4. doi: 10.1186/1755-8794-4-4.

2.

Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.

Irvin MR, Wineinger NE, Rice TK, Pajewski NM, Kabagambe EK, Gu CC, Pankow J, North KE, Wilk JB, Freedman BI, Franceschini N, Broeckel U, Tiwari HK, Arnett DK.

PLoS One. 2011;6(8):e24052. doi: 10.1371/journal.pone.0024052. Epub 2011 Aug 25.

3.

Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study.

Wineinger NE, Pajewski NM, Kennedy RE, Wojczynski MK, Vaughan LK, Hunt SC, Gu CC, Rao DC, Lorier R, Broeckel U, Arnett DK, Tiwari HK.

Eur J Hum Genet. 2011 Dec;19(12):1271-5. doi: 10.1038/ejhg.2011.115. Epub 2011 Jun 15.

4.

Copy number variations associated with obesity-related traits in African Americans: a joint analysis between GENOA and HyperGEN.

Zhao W, Wineinger NE, Tiwari HK, Mosley TH, Broeckel U, Arnett DK, Kardia SL, Kabagambe EK, Sun YV.

Obesity (Silver Spring). 2012 Dec;20(12):2431-7. doi: 10.1038/oby.2012.162. Epub 2012 Jun 22.

5.

A genome scan for linkage with aortic root diameter in hypertensive African Americans and whites in the Hypertension Genetic Epidemiology Network (HyperGEN) study.

Lynch AI, Arnett DK, Atwood LD, Devereux RB, Kitzman DW, Hopkins PN, Oberman A, Rao DC.

Am J Hypertens. 2005 May;18(5 Pt 1):627-32.

PMID:
15882545
6.

Genetic and environmental factors are associated with serum 25-hydroxyvitamin D concentrations in older African Americans.

Hansen JG, Tang W, Hootman KC, Brannon PM, Houston DK, Kritchevsky SB, Harris TB, Garcia M, Lohman K, Liu Y, de Boer IH, Kestenbaum BR, Robinson-Cohen C, Siscovick DS, Cassano PA.

J Nutr. 2015 Apr;145(4):799-805. doi: 10.3945/jn.114.202093. Epub 2015 Feb 25.

7.

Genome-wide association study of platelet aggregation in African Americans.

Qayyum R, Becker LC, Becker DM, Faraday N, Yanek LR, Leal SM, Shaw C, Mathias R, Suktitipat B, Bray PF.

BMC Genet. 2015 May 30;16:58. doi: 10.1186/s12863-015-0217-9.

8.

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.

9.

A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction.

Taylor JY, Schwander K, Kardia SL, Arnett D, Liang J, Hunt SC, Rao DC, Sun YV.

Sci Rep. 2016 Jan 11;6:18812. doi: 10.1038/srep18812.

10.

Non-replication study of a genome-wide association study for hypertension and blood pressure in African Americans.

Kidambi S, Ghosh S, Kotchen JM, Grim CE, Krishnaswami S, Kaldunski ML, Cowley AW Jr, Patel SB, Kotchen TA.

BMC Med Genet. 2012 Apr 11;13:27. doi: 10.1186/1471-2350-13-27.

11.

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.

12.

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.

13.

Genome-wide association of BMI in African Americans.

Ng MC, Hester JM, Wing MR, Li J, Xu J, Hicks PJ, Roh BH, Lu L, Divers J, Langefeld CD, Freedman BI, Palmer ND, Bowden DW.

Obesity (Silver Spring). 2012 Mar;20(3):622-7. doi: 10.1038/oby.2011.154. Epub 2011 Jun 23.

14.

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.

15.

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
16.

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
17.

Evaluation of genome-wide association study-identified type 2 diabetes loci in African Americans.

Long J, Edwards T, Signorello LB, Cai Q, Zheng W, Shu XO, Blot WJ.

Am J Epidemiol. 2012 Dec 1;176(11):995-1001. doi: 10.1093/aje/kws176. Epub 2012 Nov 9.

18.

Prostate cancer risk allele specific for African descent associates with pathologic stage at prostatectomy.

Whitman EJ, Pomerantz M, Chen Y, Chamberlin MM, Furusato B, Gao C, Ali A, Ravindranath L, Dobi A, Sesterhenn IA, McLeod DG, Srivastava S, Freedman M, Petrovics G.

Cancer Epidemiol Biomarkers Prev. 2010 Jan;19(1):1-8. doi: 10.1158/1055-9965.EPI-08-1111. Erratum in: Cancer Epidemiol Biomarkers Prev. 2010 Mar;19(3):890. Sestrehenn, Isabell A [corrected to Sesterhenn, Isabell A].

19.

Acetylcholine-metabolizing butyrylcholinesterase (BCHE) copy number and single nucleotide polymorphisms and their role in attention-deficit/hyperactivity syndrome.

Jacob CP, Weber H, Retz W, Kittel-Schneider S, Heupel J, Renner T, Lesch KP, Reif A.

J Psychiatr Res. 2013 Dec;47(12):1902-8. doi: 10.1016/j.jpsychires.2013.08.006. Epub 2013 Aug 30.

PMID:
24041656
20.

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.

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