Collapsing Approaches for the Association Analysis of Rare Variants
暂无分享,去创建一个
[1] P. Bork,et al. A method and server for predicting damaging missense mutations , 2010, Nature Methods.
[2] J. Pritchard. Are rare variants responsible for susceptibility to complex diseases? , 2001, American journal of human genetics.
[3] Claudia Hemmelmann,et al. Statistical analysis of rare sequence variants: an overview of collapsing methods , 2011, Genetic epidemiology.
[4] V. Bansal,et al. Statistical analysis strategies for association studies involving rare variants , 2010, Nature Reviews Genetics.
[5] Fiona Cunningham,et al. A Combined Functional Annotation Score for Non-Synonymous Variants , 2012, Human Heredity.
[6] P. Stanier,et al. A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia , 2009, Journal of Medical Genetics.
[7] Eleftheria Zeggini,et al. Rare variant association analysis methods for complex traits. , 2010, Annual review of genetics.
[8] Lee-Jen Wei,et al. Pooled Association Tests for Rare Variants in Exon-Resequencing Studies , 2010 .
[9] Yun Li,et al. Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes. , 2010, American journal of human genetics.
[10] K. Van Steen,et al. Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population , 2011, PloS one.
[11] Eleftheria Zeggini,et al. ARIEL and AMELIA: Testing for an Accumulation of Rare Variants Using Next-Generation Sequencing Data , 2012, Human Heredity.
[12] Dara G Torgerson,et al. Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility. , 2009, The Journal of allergy and clinical immunology.
[13] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[14] K. Mossman. The Wellcome Trust Case Control Consortium, U.K. , 2008 .
[15] 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.
[16] Yurii S. Aulchenko,et al. The Empirical Power of Rare Variant Association Methods: Results from Sanger Sequencing in 1,998 Individuals , 2012, PLoS genetics.
[17] R. Mägi,et al. Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases , 2012, Genetic epidemiology.
[18] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[19] W. Thilly,et al. A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). , 2007, Mutation research.
[20] Wei Pan,et al. A Data-Adaptive Sum Test for Disease Association with Multiple Common or Rare Variants , 2010, Human Heredity.
[21] E. Zeggini,et al. Functional annotation of non-coding sequence variants , 2014, Nature Methods.
[22] S. Browning,et al. A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic , 2009, PLoS genetics.
[23] Gang Shi,et al. Optimum designs for next‐generation sequencing to discover rare variants for common complex disease , 2011, Genetic epidemiology.
[24] Andrew D. Johnson,et al. Whole Genome Sequence-Based Analysis of a Model Complex Trait, High Density Lipoprotein Cholesterol , 2013, Nature Genetics.
[25] E. Boerwinkle,et al. Mining gold dust under the genome wide significance level: a two‐stage approach to analysis of GWAS , 2011, Genetic epidemiology.
[26] Claudio J. Verzilli,et al. An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People , 2012, Science.
[27] Steven Henikoff,et al. SIFT: predicting amino acid changes that affect protein function , 2003, Nucleic Acids Res..
[28] V. Salomaa,et al. Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia , 2010, Nature Genetics.
[29] Shuanglin Zhang,et al. Two Adaptive Weighting Methods to Test for Rare Variant Associations in Family‐Based Designs , 2012, Genetic epidemiology.
[30] E. Grice,et al. A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk , 2005, Nature.
[31] E. Zeggini,et al. An Evaluation of Statistical Approaches to Rare Variant Analysis in Genetic Association Studies , 2009, Genetic epidemiology.
[32] P. Bork,et al. Human non-synonymous SNPs: server and survey. , 2002, Nucleic acids research.