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Items: 1 to 20 of 25

1.

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries.

Park JH, Wacholder S, Gail MH, Peters U, Jacobs KB, Chanock SJ, Chatterjee N.

Nat Genet. 2010 Jul;42(7):570-5. doi: 10.1038/ng.610. Epub 2010 Jun 20.

2.

Avoiding the high Bonferroni penalty in genome-wide association studies.

Gao X, Becker LC, Becker DM, Starmer JD, Province MA.

Genet Epidemiol. 2010 Jan;34(1):100-5. doi: 10.1002/gepi.20430.

3.

Rapid and accurate multiple testing correction and power estimation for millions of correlated markers.

Han B, Kang HM, Eskin E.

PLoS Genet. 2009 Apr;5(4):e1000456. doi: 10.1371/journal.pgen.1000456. Epub 2009 Apr 17.

4.

Expansion of the human mu-opioid receptor gene architecture: novel functional variants.

Shabalina SA, Zaykin DV, Gris P, Ogurtsov AY, Gauthier J, Shibata K, Tchivileva IE, Belfer I, Mishra B, Kiselycznyk C, Wallace MR, Staud R, Spiridonov NA, Max MB, Goldman D, Fillingim RB, Maixner W, Diatchenko L.

Hum Mol Genet. 2009 Mar 15;18(6):1037-51. doi: 10.1093/hmg/ddn439. Epub 2008 Dec 22.

5.

Bayes factors for genome-wide association studies: comparison with P-values.

Wakefield J.

Genet Epidemiol. 2009 Jan;33(1):79-86. doi: 10.1002/gepi.20359.

PMID:
18642345
6.

On multiple-testing correction in genome-wide association studies.

Moskvina V, Schmidt KM.

Genet Epidemiol. 2008 Sep;32(6):567-73. doi: 10.1002/gepi.20331.

PMID:
18425821
7.

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants.

Pe'er I, Yelensky R, Altshuler D, Daly MJ.

Genet Epidemiol. 2008 May;32(4):381-5. doi: 10.1002/gepi.20303.

PMID:
18348202
8.

Estimation of significance thresholds for genomewide association scans.

Dudbridge F, Gusnanto A.

Genet Epidemiol. 2008 Apr;32(3):227-34. doi: 10.1002/gepi.20297.

9.

Reporting and interpretation in genome-wide association studies.

Wakefield J.

Int J Epidemiol. 2008 Jun;37(3):641-53. doi: 10.1093/ije/dym257. Epub 2008 Feb 11.

PMID:
18270206
10.

Probability of detecting disease-associated single nucleotide polymorphisms in case-control genome-wide association studies.

Gail MH, Pfeiffer RM, Wheeler W, Pee D.

Biostatistics. 2008 Apr;9(2):201-15. Epub 2007 Sep 14.

PMID:
17873152
11.

A Bayesian measure of the probability of false discovery in genetic epidemiology studies.

Wakefield J.

Am J Hum Genet. 2007 Aug;81(2):208-27. Epub 2007 Jul 3. Erratum in: Am J Hum Genet. 2008 Sep;83(3):424.

12.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Wellcome Trust Case Control Consortium..

Nature. 2007 Jun 7;447(7145):661-78.

13.

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.

Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, Hankinson SE, Wacholder S, Wang Z, Welch R, Hutchinson A, Wang J, Yu K, Chatterjee N, Orr N, Willett WC, Colditz GA, Ziegler RG, Berg CD, Buys SS, McCarty CA, Feigelson HS, Calle EE, Thun MJ, Hayes RB, Tucker M, Gerhard DS, Fraumeni JF Jr, Hoover RN, Thomas G, Chanock SJ.

Nat Genet. 2007 Jul;39(7):870-4. Epub 2007 May 27.

14.

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.

Yeager M, Orr N, Hayes RB, Jacobs KB, Kraft P, Wacholder S, Minichiello MJ, Fearnhead P, Yu K, Chatterjee N, Wang Z, Welch R, Staats BJ, Calle EE, Feigelson HS, Thun MJ, Rodriguez C, Albanes D, Virtamo J, Weinstein S, Schumacher FR, Giovannucci E, Willett WC, Cancel-Tassin G, Cussenot O, Valeri A, Andriole GL, Gelmann EP, Tucker M, Gerhard DS, Fraumeni JF Jr, Hoover R, Hunter DJ, Chanock SJ, Thomas G.

Nat Genet. 2007 May;39(5):645-9. Epub 2007 Apr 1.

PMID:
17401363
15.

The effects of SNP genotyping errors on the power of the Cochran-Armitage linear trend test for case/control association studies.

Ahn K, Haynes C, Kim W, Fleur RS, Gordon D, Finch SJ.

Ann Hum Genet. 2007 Mar;71(Pt 2):249-61. Epub 2006 Nov 10.

16.

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.

Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV.

Am J Hum Genet. 2006 Feb;78(2):315-33. Epub 2006 Jan 3.

17.

Ranks of genuine associations in whole-genome scans.

Zaykin DV, Zhivotovsky LA.

Genetics. 2005 Oct;171(2):813-23. Epub 2005 Jul 14.

18.

Two-stage designs for gene-disease association studies with sample size constraints.

Satagopan JM, Venkatraman ES, Begg CB.

Biometrics. 2004 Sep;60(3):589-97.

PMID:
15339280
20.

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies.

Wacholder S, Chanock S, Garcia-Closas M, El Ghormli L, Rothman N.

J Natl Cancer Inst. 2004 Mar 17;96(6):434-42.

PMID:
15026468

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