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Results: 1 to 20 of 27

References for PMC Articles for PubMed (Select 21836165)

1.

Design and implementation of the Hispanic Community Health Study/Study of Latinos.

Sorlie PD, Avil├ęs-Santa LM, Wassertheil-Smoller S, Kaplan RC, Daviglus ML, Giachello AL, Schneiderman N, Raij L, Talavera G, Allison M, Lavange L, Chambless LE, Heiss G.

Ann Epidemiol. 2010 Aug;20(8):629-41. doi: 10.1016/j.annepidem.2010.03.015.

2.

Genome-wide association studies in diverse populations.

Rosenberg NA, Huang L, Jewett EM, Szpiech ZA, Jankovic I, Boehnke M.

Nat Rev Genet. 2010 May;11(5):356-66. doi: 10.1038/nrg2760. Review.

3.

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.

Denny JC, Ritchie MD, Basford MA, Pulley JM, Bastarache L, Brown-Gentry K, Wang D, Masys DR, Roden DM, Crawford DC.

Bioinformatics. 2010 May 1;26(9):1205-10. doi: 10.1093/bioinformatics/btq126. Epub 2010 Mar 24.

4.

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.

Wang K, Baldassano R, Zhang H, Qu HQ, Imielinski M, Kugathasan S, Annese V, Dubinsky M, Rotter JI, Russell RK, Bradfield JP, Sleiman PM, Glessner JT, Walters T, Hou C, Kim C, Frackelton EC, Garris M, Doran J, Romano C, Catassi C, Van Limbergen J, Guthery SL, Denson L, Piccoli D, Silverberg MS, Stanley CA, Monos D, Wilson DC, Griffiths A, Grant SF, Satsangi J, Polychronakos C, Hakonarson H.

Hum Mol Genet. 2010 May 15;19(10):2059-67. doi: 10.1093/hmg/ddq078. Epub 2010 Feb 22.

5.

Association of blood lipids with common DNA sequence variants at 19 genetic loci in the multiethnic United States National Health and Nutrition Examination Survey III.

Keebler ME, Sanders CL, Surti A, Guiducci C, Burtt NP, Kathiresan S.

Circ Cardiovasc Genet. 2009 Jun;2(3):238-43. doi: 10.1161/CIRCGENETICS.108.829473. Epub 2009 Apr 14.

6.

Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.

Shriner D, Adeyemo A, Gerry NP, Herbert A, Chen G, Doumatey A, Huang H, Zhou J, Christman MF, Rotimi CN.

PLoS One. 2009 Dec 22;4(12):e8398. doi: 10.1371/journal.pone.0008398.

7.

Meta-analysis of genome-wide association studies: no efficiency gain in using individual participant data.

Lin DY, Zeng D.

Genet Epidemiol. 2010 Jan;34(1):60-6. doi: 10.1002/gepi.20435.

8.

Next generation disparities in human genomics: concerns and remedies.

Need AC, Goldstein DB.

Trends Genet. 2009 Nov;25(11):489-94. doi: 10.1016/j.tig.2009.09.012.

PMID:
19836853
9.

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA.

Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9362-7. doi: 10.1073/pnas.0903103106. Epub 2009 May 27.

10.

Human genetic variation and its contribution to complex traits.

Frazer KA, Murray SS, Schork NJ, Topol EJ.

Nat Rev Genet. 2009 Apr;10(4):241-51. doi: 10.1038/nrg2554. Review.

PMID:
19293820
11.

Beyond odds ratios--communicating disease risk based on genetic profiles.

Kraft P, Wacholder S, Cornelis MC, Hu FB, Hayes RB, Thomas G, Hoover R, Hunter DJ, Chanock S.

Nat Rev Genet. 2009 Apr;10(4):264-9. doi: 10.1038/nrg2516.

PMID:
19238176
12.

Genetic mapping in human disease.

Altshuler D, Daly MJ, Lander ES.

Science. 2008 Nov 7;322(5903):881-8. doi: 10.1126/science.1156409. Review.

13.

Genome-wide association studies: potential next steps on a genetic journey.

McCarthy MI, Hirschhorn JN.

Hum Mol Genet. 2008 Oct 15;17(R2):R156-65. doi: 10.1093/hmg/ddn289. Review.

14.

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.

Homer N, Szelinger S, Redman M, Duggan D, Tembe W, Muehling J, Pearson JV, Stephan DA, Nelson SF, Craig DW.

PLoS Genet. 2008 Aug 29;4(8):e1000167. doi: 10.1371/journal.pgen.1000167.

15.

Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America.

Kosoy R, Nassir R, Tian C, White PA, Butler LM, Silva G, Kittles R, Alarcon-Riquelme ME, Gregersen PK, Belmont JW, De La Vega FM, Seldin MF.

Hum Mutat. 2009 Jan;30(1):69-78. doi: 10.1002/humu.20822.

16.

The NCBI dbGaP database of genotypes and phenotypes.

Mailman MD, Feolo M, Jin Y, Kimura M, Tryka K, Bagoutdinov R, Hao L, Kiang A, Paschall J, Phan L, Popova N, Pretel S, Ziyabari L, Lee M, Shao Y, Wang ZY, Sirotkin K, Ward M, Kholodov M, Zbicz K, Beck J, Kimelman M, Shevelev S, Preuss D, Yaschenko E, Graeff A, Ostell J, Sherry ST.

Nat Genet. 2007 Oct;39(10):1181-6.

17.

Overcoming the winner's curse: estimating penetrance parameters from case-control data.

Zollner S, Pritchard JK.

Am J Hum Genet. 2007 Apr;80(4):605-15. Epub 2007 Feb 16.

18.

Principal components analysis corrects for stratification in genome-wide association studies.

Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D.

Nat Genet. 2006 Aug;38(8):904-9. Epub 2006 Jul 23.

PMID:
16862161
19.

'Racial' differences in genetic effects for complex diseases.

Ioannidis JP, Ntzani EE, Trikalinos TA.

Nat Genet. 2004 Dec;36(12):1312-8. Epub 2004 Nov 14.

PMID:
15543147
20.

Genetic and environmental contributions to cardiovascular disease risk in American Indians: the strong heart family study.

North KE, Howard BV, Welty TK, Best LG, Lee ET, Yeh JL, Fabsitz RR, Roman MJ, MacCluer JW.

Am J Epidemiol. 2003 Feb 15;157(4):303-14.

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