Polygenic modeling of genome-wide association studies: an application to prostate and breast cancer.
暂无分享,去创建一个
[1] P. Visscher,et al. Common SNPs explain a large proportion of the heritability for human height , 2010, Nature Genetics.
[2] J. Witte. Genome-wide association studies and beyond. , 2010, Annual review of public health.
[3] W. Tilley,et al. Breast and prostate cancer: more similar than different , 2010, Nature Reviews Cancer.
[4] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[5] P. Visscher,et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder , 2009, Nature.
[6] 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.
[7] John S. Witte,et al. Prostate cancer genomics: towards a new understanding , 2009, Nature Reviews Genetics.
[8] Peter Donnelly,et al. Progress and challenges in genome-wide association studies in humans , 2008, Nature.
[9] B. Maher. Personal genomes: The case of the missing heritability , 2008, Nature.
[10] M. McCarthy,et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges , 2008, Nature Reviews Genetics.
[11] W. Willett,et al. Multiple loci identified in a genome-wide association study of prostate cancer , 2008, Nature Genetics.
[12] K. Taylor,et al. Genome-Wide Association , 2007, Diabetes.
[13] Zhaohui S. Qin,et al. A second generation human haplotype map of over 3.1 million SNPs , 2007, Nature.
[14] W. Willett,et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer , 2007, Nature Genetics.
[15] P. Fearnhead,et al. Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 , 2007, Nature Genetics.
[16] Martin S. Taylor,et al. Genome-wide genetic association of complex traits in heterogeneous stock mice , 2006, Nature Genetics.
[17] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[18] D. Schaid,et al. Description of the international consortium for prostate cancer genetics, and failure to replicate linkage of hereditary prostate cancer to 20q13 , 2005, The Prostate.
[19] M. Olivier. A haplotype map of the human genome. , 2003, Nature.
[20] M. Olivier. A haplotype map of the human genome , 2003, Nature.
[21] S. Gabriel,et al. The Structure of Haplotype Blocks in the Human Genome , 2002, Science.
[22] M. Daly,et al. High-resolution haplotype structure in the human genome , 2001, Nature Genetics.
[23] Timothy B. Stockwell,et al. The Sequence of the Human Genome , 2001, Science.
[24] J. V. Moran,et al. Initial sequencing and analysis of the human genome. , 2001, Nature.
[25] D. Heisey,et al. The Abuse of Power , 2001 .
[26] J. Witte,et al. On the relative sample size required for multiple comparisons. , 2000, Statistics in medicine.
[27] E. Lander. The New Genomics: Global Views of Biology , 1996, Science.
[28] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[29] J. Witte,et al. Genetic dissection of complex traits , 1996, Nature Genetics.
[30] N. Nagelkerke,et al. A note on a general definition of the coefficient of determination , 1991 .
[31] D. Mccormick. Sequence the Human Genome , 1986, Bio/Technology.
[32] On beyond GWAS , 2010, Nature Genetics.
[33] D. Clayton,et al. A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes. , 2002, American journal of human genetics.
[34] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.