Genetic Epidemiology

Cover image for Vol. 35 Issue 5

July 2011

Volume 35, Issue 5

Pages 291–426

  1. Original Articles

    1. Top of page
    2. Original Articles
    3. Brief Report
    1. Genetic variance components estimation for binary traits using multiple related individuals (pages 291–302)

      Charalampos Papachristou, Carole Ober and Mark Abney

      Version of Record online: 4 APR 2011 | DOI: 10.1002/gepi.20577

    2. On the follow-up of genome-wide association studies: an overall test for the most promising SNPs (pages 303–309)

      Peter J. Lipman, Michael H. Cho, Per Bakke, Amund Gulsvik, Xiangyang Kong, David A. Lomas, Wayne Anderson, Edwin K. Silverman and Christoph Lange

      Version of Record online: 3 MAR 2011 | DOI: 10.1002/gepi.20578

    3. Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases (pages 310–317)

      Hon-Cheong So, Allen H.S. Gui, Stacey S. Cherny and Pak C. Sham

      Version of Record online: 3 MAR 2011 | DOI: 10.1002/gepi.20579

    4. Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes (pages 318–332)

      Tune H. Pers, Niclas Tue Hansen, Kasper Lage, Pernille Koefoed, Piotr Dworzynski, Martin Lee Miller, Tracey J. Flint, Erling Mellerup, Henrik Dam, Ole A. Andreassen, Srdjan Djurovic, Ingrid Melle, Anders D. Børglum, Thomas Werge, Shaun Purcell, Manuel A. Ferreira, Irene Kouskoumvekaki, Christopher T. Workman, Torben Hansen, Ole Mors and Søren Brunak

      Version of Record online: 11 APR 2011 | DOI: 10.1002/gepi.20580

    5. Bayesian semiparametric meta-analysis for genetic association studies (pages 333–340)

      Maria De Iorio, Paul J. Newcombe, Ioanna Tachmazidou, Claudio J. Verzilli and John C. Whittaker

      Version of Record online: 11 MAR 2011 | DOI: 10.1002/gepi.20581

    6. Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability (pages 341–349)

      Zoltán Kutalik, John Whittaker, Dawn Waterworth, GIANT consortium, Jacques S. Beckmann and Sven Bergmann

      Version of Record online: 4 APR 2011 | DOI: 10.1002/gepi.20582

    7. An improved score test for genetic association studies (pages 350–359)

      Qiuying Sha, Zhaogong Zhang and Shuanglin Zhang

      Version of Record online: 11 APR 2011 | DOI: 10.1002/gepi.20583

    8. Linkage analysis without defined pedigrees (pages 360–370)

      Aaron G. Day-Williams, John Blangero, Thomas D. Dyer, Kenneth Lange and Eric M. Sobel

      Version of Record online: 4 APR 2011 | DOI: 10.1002/gepi.20584

    9. Fast, exact linkage analysis for categorical traits on arbitrary pedigree designs (pages 371–380)

      Abra Brisbin, Jenifer Cruickshank, N. Sydney Moïse, Teresa Gunn, Carlos D. Bustamante and Jason G. Mezey

      Version of Record online: 25 APR 2011 | DOI: 10.1002/gepi.20585

    10. Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling (pages 389–397)

      Marinela Capanu, Patrick Concannon, Robert W. Haile, Leslie Bernstein, Kathleen E. Malone, Charles F. Lynch, Xiaolin Liang, Sharon N. Teraoka, Anh T. Diep, Duncan C. Thomas, Jonine L. Bernstein, The WECARE Study Collaborative Group and Colin B. Begg

      Version of Record online: 25 APR 2011 | DOI: 10.1002/gepi.20587

    11. The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery (pages 410–422)

      S.A. Pendergrass, K. Brown-Gentry, S.M. Dudek, E.S. Torstenson, J.L. Ambite, C.L. Avery, S. Buyske, C. Cai, M.D. Fesinmeyer, C. Haiman, G. Heiss, L.A. Hindorff, C.-N. Hsu, R.D. Jackson, C. Kooperberg, L. Le Marchand, Y. Lin, T.C. Matise, L. Moreland, K. Monroe, A.P. Reiner, R. Wallace, L.R. Wilkens, D.C. Crawford and M.D. Ritchie

      Version of Record online: 18 MAY 2011 | DOI: 10.1002/gepi.20589

  2. Brief Report

    1. Top of page
    2. Original Articles
    3. Brief Report
    1. SNP mistyping in genotyping arrays—an important cause of spurious association in case-control studies (pages 423–426)

      D. Mitry, H. Campbell, D.G. Charteris, B.W. Fleck, A. Tenesa, M.G. Dunlop, C. Hayward, A.F. Wright and V. Vitart

      Version of Record online: 19 JAN 2011 | DOI: 10.1002/gepi.20559