Risk prediction using genome‐wide association studies
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Valerie Obenchain | Charles Kooperberg | Michael LeBlanc | Valerie Obenchain | M. LeBlanc | C. Kooperberg
[1] N. Cook. Use and Misuse of the Receiver Operating Characteristic Curve in Risk Prediction , 2007, Circulation.
[2] M. Gail,et al. Projecting individualized probabilities of developing breast cancer for white females who are being examined annually. , 1989, Journal of the National Cancer Institute.
[3] Arthur E. Hoerl,et al. Ridge Regression: Biased Estimation for Nonorthogonal Problems , 2000, Technometrics.
[4] J. Pritchard,et al. Overcoming the winner's curse: estimating penetrance parameters from case-control data. , 2007, American journal of human genetics.
[5] J. Chan,et al. Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association , 2009, Journal of Human Genetics.
[6] Joseph T. Glessner,et al. From Disease Association to Risk Assessment: An Optimistic View from Genome-Wide Association Studies on Type 1 Diabetes , 2009, PLoS genetics.
[7] H. Zou. The Adaptive Lasso and Its Oracle Properties , 2006 .
[8] Judy H. Cho,et al. A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene , 2006, Science.
[9] L. T. Middleton,et al. Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score—the CoLaus Study , 2009, Diabetologia.
[10] R. Tibshirani. Regression Shrinkage and Selection via the Lasso , 1996 .
[11] H. Zou,et al. Regularization and variable selection via the elastic net , 2005 .
[12] D Spiegelman,et al. Validation of the Gail et al. model of breast cancer risk prediction and implications for chemoprevention. , 2001, Journal of the National Cancer Institute.
[13] Peter Kraft,et al. Genetic risk prediction--are we there yet? , 2009, The New England journal of medicine.
[14] P. Qiu. The Statistical Evaluation of Medical Tests for Classification and Prediction , 2005 .
[15] P. Visscher,et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder , 2009, Nature.
[16] I. Johnstone,et al. Ideal spatial adaptation by wavelet shrinkage , 1994 .
[17] Judy H Cho,et al. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis , 2007, Nature Genetics.
[18] Pär Stattin,et al. Cumulative association of five genetic variants with prostate cancer. , 2008, The New England journal of medicine.
[19] Mee Young Park,et al. Penalized logistic regression for detecting gene interactions. , 2008, Biostatistics.
[20] D. Bonthron,et al. Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3. , 1994, American journal of human genetics.
[21] D Spiegelman,et al. Validation of the Gail et al. model for predicting individual breast cancer risk. , 1994, Journal of the National Cancer Institute.
[22] M. Pepe. The Statistical Evaluation of Medical Tests for Classification and Prediction , 2003 .
[23] Trevor J. Hastie,et al. Genome-wide association analysis by lasso penalized logistic regression , 2009, Bioinform..
[24] D. Ruppert. The Elements of Statistical Learning: Data Mining, Inference, and Prediction , 2004 .
[25] Nancy R. Cook,et al. Use and Misuse of the Receiver Operating Characteristic Curve in Risk Prediction , 2007, Circulation.
[26] Peter M Visscher,et al. Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. , 2009, Human molecular genetics.
[27] R. Prentice,et al. Bias-reduced estimators and confidence intervals for odds ratios in genome-wide association studies. , 2008, Biostatistics.
[28] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[29] D. L. Donoho,et al. Ideal spacial adaptation via wavelet shrinkage , 1994 .
[30] Alberto Piazza,et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants , 2009, Nature Genetics.
[31] M. Gail. Value of adding single-nucleotide polymorphism genotypes to a breast cancer risk model. , 2009, Journal of the National Cancer Institute.