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There are 42757 results for: content related to: Statistical analysis of rare sequence variants: an overview of collapsing methods

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    Likelihood Ratio Tests in Rare Variant Detection for Continuous Phenotypes

    Annals of Human Genetics

    Volume 78, Issue 5, September 2014, Pages: 320–332, Ping Zeng, Yang Zhao, Jin Liu, Liya Liu, Liwei Zhang, Ting Wang, Shuiping Huang and Feng Chen

    Version of Record online : 12 AUG 2014, DOI: 10.1111/ahg.12071

  2. Detecting Association of Rare and Common Variants by Testing an Optimally Weighted Combination of Variants

    Genetic Epidemiology

    Volume 36, Issue 6, September 2012, Pages: 561–571, Qiuying Sha, Xuexia Wang, Xinli Wang and Shuanglin Zhang

    Version of Record online : 19 JUN 2012, DOI: 10.1002/gepi.21649

  3. Rare genetic variants and treatment response: sample size and analysis issues

    Statistics in Medicine

    Volume 31, Issue 25, 10 November 2012, Pages: 3041–3050, John S. Witte

    Version of Record online : 27 JUN 2012, DOI: 10.1002/sim.5428

  4. Identifying Rare Variants Associated with Complex Traits via Sequencing

    Unit

    Current Protocols in Human Genetics

    1:1.26.1–1.26.22

    Bingshan Li, Dajiang J. Liu and Suzanne M. Leal

    Published Online : 1 JUL 2013, DOI: 10.1002/0471142905.hg0126s78

  5. Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

    Genetic Epidemiology

    Volume 36, Issue 1, January 2012, Pages: 22–35, Leah E. Mechanic, Huann-Sheng Chen, Christopher I. Amos, Nilanjan Chatterjee, Nancy J. Cox, Rao L. Divi, Ruzong Fan, Emily L. Harris, Kevin Jacobs, Peter Kraft, Suzanne M. Leal, Kimberly McAllister, Jason H. Moore, Dina N. Paltoo, Michael A. Province, Erin M. Ramos, Marylyn D. Ritchie, Kathryn Roeder, Daniel J. Schaid, Matthew Stephens, Duncan C. Thomas, Clarice R. Weinberg, John S. Witte, Shunpu Zhang, Sebastian Zöllner, Eric J. Feuer and Elizabeth M. Gillanders

    Version of Record online : 6 DEC 2011, DOI: 10.1002/gepi.20652

  6. Valid Monte Carlo Permutation Tests for Genetic Case-Control Studies With Missing Genotypes

    Genetic Epidemiology

    Volume 38, Issue 4, May 2014, Pages: 325–344, Daniel D. Kinnamon and Eden R. Martin

    Version of Record online : 10 APR 2014, DOI: 10.1002/gepi.21805

  7. Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies

    Genetic Epidemiology

    Volume 35, Issue 8, December 2011, Pages: 790–799, Dalin Li, Juan Pablo Lewinger, William J. Gauderman, Cassandra Elizabeth Murcray and David Conti

    Version of Record online : 15 SEP 2011, DOI: 10.1002/gepi.20628

  8. Bayesian analysis of rare variants in genetic association studies

    Genetic Epidemiology

    Volume 35, Issue 1, January 2011, Pages: 57–69, Nengjun Yi and Degui Zhi

    Version of Record online : 22 DEC 2010, DOI: 10.1002/gepi.20554

  9. Re-sequencing of ankyrin 3 exon 48 and case-control association analysis of rare variants in bipolar disorder type I

    Bipolar Disorders

    Volume 14, Issue 8, December 2012, Pages: 809–821, Glenn A Doyle, Alison T Lai, Andrew D Chou, Min-Jung Wang, Xiaowu Gai, Eric F Rappaport and Wade H Berrettini

    Version of Record online : 11 SEP 2012, DOI: 10.1111/bdi.12002

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    The 2015 Annual Meeting of the International Genetic Epidemiology Society

    Genetic Epidemiology

    Volume 39, Issue 7, November 2015, Pages: 529–599,

    Version of Record online : 14 SEP 2015, DOI: 10.1002/gepi.21916

  11. You have free access to this content
    PreCimp: Pre-collapsing imputation approach increases imputation accuracy of rare variants in terms of collapsed variables

    Genetic Epidemiology

    Volume 41, Issue 1, January 2017, Pages: 41–50, Young Jin Kim, Juyoung Lee, Bong-Jo Kim, T2D-Genes Consortium and Taesung Park

    Version of Record online : 10 NOV 2016, DOI: 10.1002/gepi.22020

  12. Kernel-Machine Testing Coupled with a Rank-Truncation Method for Genetic Pathway Analysis

    Genetic Epidemiology

    Volume 38, Issue 5, July 2014, Pages: 447–456, Qi Yan, Hemant K. Tiwari, Nengjun Yi, Wan-Yu Lin, Guimin Gao, Xiang-Yang Lou, Xiangqin Cui and Nianjun Liu

    Version of Record online : 21 MAY 2014, DOI: 10.1002/gepi.21813

  13. A Generalized Genetic Random Field Method for the Genetic Association Analysis of Sequencing Data

    Genetic Epidemiology

    Volume 38, Issue 3, April 2014, Pages: 242–253, Ming Li, Zihuai He, Min Zhang, Xiaowei Zhan, Changshuai Wei, Robert C. Elston and Qing Lu

    Version of Record online : 30 JAN 2014, DOI: 10.1002/gepi.21790

  14. A Variational Bayes Discrete Mixture Test for Rare Variant Association

    Genetic Epidemiology

    Volume 38, Issue 1, January 2014, Pages: 21–30, Benjamin A. Logsdon, James Y. Dai, Paul L. Auer, Jill M. Johnsen, Santhi K. Ganesh, Nicholas L. Smith, James G. Wilson, Russell P. Tracy, Leslie A. Lange, Shuo Jiao, Stephen S. Rich, Guillaume Lettre, Christopher S. Carlson, Rebecca D. Jackson, Christopher J. O'Donnell, Mark M. Wurfel, Deborah A. Nickerson, Hua Tang, Alexander P. Reiner, Charles Kooperberg and on behalf of the NHLBI GO Exome Sequencing Project

    Version of Record online : 25 NOV 2013, DOI: 10.1002/gepi.21772

  15. Power of Family-Based Association Designs to Detect Rare Variants in Large Pedigrees Using Imputed Genotypes

    Genetic Epidemiology

    Volume 38, Issue 1, January 2014, Pages: 1–9, Mohamad Saad and Ellen M. Wijsman

    Version of Record online : 15 NOV 2013, DOI: 10.1002/gepi.21776

  16. The Value of Statistical or Bioinformatics Annotation for Rare Variant Association With Quantitative Trait

    Genetic Epidemiology

    Volume 37, Issue 7, November 2013, Pages: 666–674, Andrea E. Byrnes, Michael C. Wu, Fred A. Wright, Mingyao Li and Yun Li

    Version of Record online : 8 JUL 2013, DOI: 10.1002/gepi.21747

  17. A Novel Test for Testing the Optimally Weighted Combination of Rare and Common Variants Based on Data of Parents and Affected Children

    Genetic Epidemiology

    Volume 38, Issue 2, February 2014, Pages: 135–143, Qiuying Sha and Shuanglin Zhang

    Version of Record online : 30 DEC 2013, DOI: 10.1002/gepi.21787

  18. ANNUAL MEETING OF THE INTERNATIONAL GENETIC EPIDEMIOLOGY SOCIETY

    Genetic Epidemiology

    Volume 36, Issue 2, February 2012, Pages: 118–171,

    Version of Record online : 26 JAN 2012, DOI: 10.1002/gepi.21604

  19. Investigation of the role of TCF4 rare sequence variants in schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 5, July 2015, Pages: 354–362, F. Buket Basmanav, Andreas J. Forstner, Heide Fier, Stefan Herms, Sandra Meier, Franziska Degenhardt, Per Hoffmann, Sandra Barth, Nadine Fricker, Jana Strohmaier, Stephanie H. Witt, Michael Ludwig, Christine Schmael, Susanne Moebus, Wolfgang Maier, Rainald Mössner, Dan Rujescu, Marcella Rietschel, Christoph Lange, Markus M. Nöthen and Sven Cichon

    Version of Record online : 22 MAY 2015, DOI: 10.1002/ajmg.b.32318

  20. Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 7, October 2015, Pages: 544–556, Lingjun Zuo, Laura Saba, Xiandong Lin, Yunlong Tan, Kesheng Wang, John H. Krystal, Boris Tabakoff and Xingguang Luo

    Version of Record online : 16 JUN 2015, DOI: 10.1002/ajmg.b.32329