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Results: 1-7 |
Results: 7
Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
Authors: Wu, Michael C. Lee, Seunggeun Cai, Tianxi Li, Yun
Citation: C. Wu, Michael et al., Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test, American journal of human genetics (Online) AJHG , 89(1), 2011, pp. 82-93
Bayesian inference for causal mediation effects using principal stratification with dichotomous mediators and outcomes
Authors: Elliott, Michael R. Raghunathan, Trivellore E. Li, Yun
Citation: R. Elliott, Michael et al., Bayesian inference for causal mediation effects using principal stratification with dichotomous mediators and outcomes, Biostatistics (Oxford. Print) , 11(2), 2010, pp. 353-372
Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta
Authors: Becker, Jutta Semler, Oliver Gilissen, Christian Li, Yun Netzer, Christian
Citation: Becker, Jutta et al., Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta, American journal of human genetics (Online) AJHG , 88(3), 2011, pp. 362-371
Causal assessment of surrogacy in a meta-analysis of colorectal cancer trials
Authors: Li, Yun Taylor, Jeremy M.G. Elliott, Michael R. Sargent, Daniel J.
Citation: Li, Yun et al., Causal assessment of surrogacy in a meta-analysis of colorectal cancer trials, Biostatistics (Oxford. Print) , 12(3), 2011, pp. 478-492
Extending Rare-Variant Testing Strategies: Analysis of Noncoding Sequence and Imputed Genotypes
Authors: Zawistowski, Matthew Gopalakrishnan, Shyam Ding, Jun Li, Yun Zöllner, Sebastian
Citation: Zawistowski, Matthew et al., Extending Rare-Variant Testing Strategies: Analysis of Noncoding Sequence and Imputed Genotypes, American journal of human genetics (Online) AJHG , 87(5), 2010, pp. 604-617
To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests
Authors: Li, Yun Byrnes, Andrea E. Li, Mingyao
Citation: Li, Yun et al., To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests, American journal of human genetics (Online) AJHG , 87(5), 2010, pp. 728-735
Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling
Authors: Li, Yun Laue, Kathrin Temtamy, Samia Aglan, Mona Wollnik, Bernd
Citation: Li, Yun et al., Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling, American journal of human genetics (Online) AJHG , 87(6), 2010, pp. 757-767
Risultati: 1-7 |