General framework for meta-analysis of rare variants in sequencing association studies.
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Seunggeun Lee | Tanya M. Teslovich | Michael Boehnke | Xihong Lin | Xihong Lin | M. Boehnke | Seunggeun Lee | Tanya M Teslovich
[1] John P A Ioannidis,et al. Meta-analysis in genome-wide association studies. , 2009, Pharmacogenomics.
[2] Wolfgang Viechtbauer,et al. Conducting Meta-Analyses in R with the metafor Package , 2010 .
[3] Meta-Analysis of Gene Level Association Tests , 2013, 1305.1318.
[4] K. Mossman. The Wellcome Trust Case Control Consortium, U.K. , 2008 .
[5] Eleazar Eskin,et al. Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. , 2011, American journal of human genetics.
[6] S. Leal,et al. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. , 2008, American journal of human genetics.
[7] Xihong Lin,et al. Hypothesis testing in semiparametric additive mixed models. , 2003, Biostatistics.
[8] E. Suchman,et al. The American Soldier: Adjustment During Army Life. , 1949 .
[9] Tanya M. Teslovich,et al. Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids , 2010, Nature.
[10] A. Morris,et al. Transethnic Meta-Analysis of Genomewide Association Studies , 2011, Genetic epidemiology.
[11] W. Ansorge. Next-generation DNA sequencing techniques. , 2009, New biotechnology.
[12] M. Rieder,et al. Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. , 2012, American journal of human genetics.
[13] Kathryn Roeder,et al. Testing for an Unusual Distribution of Rare Variants , 2011, PLoS genetics.
[14] P. Bork,et al. A method and server for predicting damaging missense mutations , 2010, Nature Methods.
[15] F. Collins,et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.
[16] G. Tseng,et al. Comprehensive literature review and statistical considerations for GWAS meta-analysis , 2012, Nucleic acids research.
[17] Yurii S. Aulchenko,et al. The Empirical Power of Rare Variant Association Methods: Results from Sanger Sequencing in 1,998 Individuals , 2012, PLoS genetics.
[18] P. Visscher,et al. Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits , 2012, Nature Genetics.
[19] M. McCarthy,et al. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes , 2008, Nature Genetics.
[20] M. McCarthy,et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges , 2008, Nature Reviews Genetics.
[21] Education Division. Studies in social psychology in World War II , 1949 .
[22] Xihong Lin,et al. Optimal tests for rare variant effects in sequencing association studies. , 2012, Biostatistics.
[23] D Y Lin,et al. Meta‐analysis of genome‐wide association studies: no efficiency gain in using individual participant data , 2009, Genetic epidemiology.
[24] Jing Cui,et al. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci , 2010, Nature Genetics.
[25] Kathryn Roeder,et al. Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls , 2013, PLoS genetics.
[26] Evangelos Evangelou,et al. Heterogeneity in Meta-Analyses of Genome-Wide Association Investigations , 2007, PloS one.
[27] Tatiana A. Tatusova,et al. NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy , 2011, Nucleic Acids Res..
[28] Josyf Mychaleckyj,et al. Robust relationship inference in genome-wide association studies , 2010, Bioinform..
[29] S. Browning,et al. A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic , 2009, PLoS genetics.
[30] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[31] R. Fisher. Statistical methods for research workers , 1927, Protoplasma.
[32] S. Gabriel,et al. Calibrating a coalescent simulation of human genome sequence variation. , 2005, Genome research.
[33] Zhaohui S. Qin,et al. A second generation human haplotype map of over 3.1 million SNPs , 2007, Nature.
[34] R. Davies. The distribution of a linear combination of 2 random variables , 1980 .
[35] Lei Sun,et al. Robust and Powerful Tests for Rare Variants Using Fisher's Method to Combine Evidence of Association From Two or More Complementary Tests , 2013, Genetic epidemiology.
[36] S. Henikoff,et al. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm , 2009, Nature Protocols.
[37] Pierre Lafaye de Micheaux,et al. Computing the distribution of quadratic forms: Further comparisons between the Liu-Tang-Zhang approximation and exact methods , 2010, Comput. Stat. Data Anal..
[38] Xihong Lin,et al. Rare-variant association testing for sequencing data with the sequence kernel association test. , 2011, American journal of human genetics.
[39] Lee-Jen Wei,et al. Pooled Association Tests for Rare Variants in Exon-Resequencing Studies , 2010 .