SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Xiaohong Fan, Zhijun Wu, Effects of four single nucleotide polymorphisms in microRNA-coding genes on lung cancer risk, Tumor Biology, 2014, 35, 11, 10815

    CrossRef

  2. 2
    Minjung Kwak, Robust suptest for the genetic association study under genetic model uncertainty, Journal of the Korean Statistical Society, 2014, 43, 3, 463

    CrossRef

  3. 3
    Yu Jiang, Glen A. Satten, Yujun Han, Michael P. Epstein, Erin L. Heinzen, David B. Goldstein, Andrew S. Allen, Utilizing Population Controls in Rare-Variant Case-Parent Association Tests, The American Journal of Human Genetics, 2014, 94, 6, 845

    CrossRef

  4. 4
    Yuqing Lou, Rong Li, Yanwei Zhang, Runbo Zhong, Jun Pei, Liwen Xiong, Xueyan Zhang, Baohui Han, XPA gene rs1800975 single nucleotide polymorphism and lung cancer risk: a meta-analysis, Tumor Biology, 2014, 35, 7, 6607

    CrossRef

  5. 5
    F. Haerynck, J.M. Mahachie John, K. Van Steen, P. Schelstraete, S. Van daele, B. Loeys, M. Van Thielen, I. De Canck, L. Nuytinck, F. De Baets, Genetic variations in toll-like receptor pathway and lung function decline in Cystic Fibrosis patients, Human Immunology, 2013, 74, 12, 1649

    CrossRef

  6. 6
    Sang Mee Lee, Theodore G. Karrison, Nancy J. Cox, Hae Kyung Im, Quantitative Allelic Test—A Fast Test for Very Large Association Studies, Genetic Epidemiology, 2013, 37, 8
  7. 7
    Rafael Izbicki, Victor Fossaluza, Ana Gabriela Hounie, Eduardo Yoshio Nakano, Carlos Alberto de Bragança Pereira, Testing allele homogeneity: the problem of nested hypotheses, BMC Genetics, 2012, 13, 1, 103

    CrossRef

  8. 8
    Anke Hinney, André Scherag, Ivonne Jarick, Özgür Albayrak, Carolin Pütter, Sonali Pechlivanis, Maria R. Dauvermann, Sebastian Beck, Heike Weber, Susann Scherag, Trang T. Nguyen, Anna-Lena Volckmar, Nadja Knoll, Stephen V. Faraone, Benjamin M. Neale, Barbara Franke, Sven Cichon, Per Hoffmann, Markus M. Nöthen, Stefan Schreiber, Karl-Heinz Jöckel, H.-Erich Wichmann, Christine Freitag, Thomas Lempp, Jobst Meyer, Susanne Gilsbach, Beate Herpertz-Dahlmann, Judith Sinzig, Gerd Lehmkuhl, Tobias J. Renner, Andreas Warnke, Marcel Romanos, Klaus-Peter Lesch, Andreas Reif, Benno G. Schimmelmann, Johannes Hebebrand, Genome-wide association study in German patients with attention deficit/hyperactivity disorder, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2011, 156, 8
  9. 9
    Yijun Zuo, Guolian Kang, A mixed two-stage method for detecting interactions in genomewide association studies, Journal of Theoretical Biology, 2010, 262, 4, 576

    CrossRef

  10. 10
    Philipp D. Koellinger, Matthijs J. H. M. van der Loos, Patrick J. F. Groenen, A. Roy Thurik, Fernando Rivadeneira, Frank J. A. van Rooij, André G. Uitterlinden, Albert Hofman, Genome-wide association studies in economics and entrepreneurship research: promises and limitations, Small Business Economics, 2010, 35, 1, 1

    CrossRef

  11. 11
    Dmitri V. Zaykin, Damian O. Kozbur, P-value based analysis for shared controls design in genome-wide association studies, Genetic Epidemiology, 2010, 34, 7
  12. 12
    Gang Zheng, Jungnam Joo, Yaning Yang, Pearson's Test, Trend Test, and MAX Are All Trend Tests with Different Types of Scores, Annals of Human Genetics, 2009, 73, 2
  13. 13
    Gang Zheng, Can the Allelic Test be Retired from Analysis of Case-Control Association Studies?, Annals of Human Genetics, 2008, 72, 6
  14. 14
    Erratum, Annals of Human Genetics, 2008, 72, 5
  15. 15
    Michael Knapp, On the asymptotic equivalence of allelic and trend statistic under Hardy-Weinberg equilibrium, Annals of Human Genetics, 2008, 72, 5
  16. 16
    References,