Works matching IS 07410395 AND DT 2011 AND VI 35 AND IP 3

Results: 9

On optimal pooling designs to identify rare variants through massive resequencing.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 139, doi. 10.1002/gepi.20561

By:

Lee, Joon Sang;
Choi, Murim;
Yan, Xiting;
Lifton, Richard P.;
Zhao, Hongyu

Publication type:

Article

Quantifying and correcting for the winner's curse in quantitative-trait association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 133, doi. 10.1002/gepi.20551

By:

Xiao, Rui;
Boehnke, Michael

Publication type:

Article

Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 182, doi. 10.1002/gepi.20566

By:

Bureau, Alexandre;
Croteau, Jordie;
Tayeb, Arafat;
Mérette, Chantal;
Labbe, Aurélie

Publication type:

Article

Sampling GWAS subjects from risk populations.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 148, doi. 10.1002/gepi.20562

By:

Oexle, Konrad;
Meitinger, Thomas

Publication type:

Article

Validity and power of association testing in family-based sampling designs: evidence for and against the common wisdom.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 174, doi. 10.1002/gepi.20565

By:

Knight, Stacey;
Camp, Nicola J.

Publication type:

Article

Phenotype harmonization and cross-study collaboration in GWAS consortia: the GENEVA experience.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 159, doi. 10.1002/gepi.20564

By:

Bennett, Siiri N.;
Caporaso, Neil;
Fitzpatrick, Annette L.;
Agrawal, Arpana;
Barnes, Kathleen;
Boyd, Heather A.;
Cornelis, Marilyn C.;
Hansel, Nadia N.;
Heiss, Gerardo;
Heit, John A.;
Kang, Jae Hee;
Kittner, Steven J.;
Kraft, Peter;
Lowe, William;
Marazita, Mary L.;
Monroe, Kristine R.;
Pasquale, Louis R.;
Ramos, Erin M.;
van Dam, Rob M.;
Udren, Jenna

Publication type:

Article

Estimation of odds ratios of genetic variants for the secondary phenotypes associated with primary diseases.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 190, doi. 10.1002/gepi.20568

By:

Wang, Jian;
Shete, Sanjay

Publication type:

Article

Multiple testing corrections for imputed SNPs.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 154, doi. 10.1002/gepi.20563

By:

Gao, Xiaoyi

Publication type:

Article

Sample size requirements to detect gene-environment interactions in genome-wide association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 3, p. 201, doi. 10.1002/gepi.20569

By:

Murcray, Cassandra E.;
Lewinger, Juan Pablo;
Conti, David V.;
Thomas, Duncan C.;
Gauderman, W. James

Publication type:

Article