Inclusion of gene-gene and gene-environment interactions unlikely to dramatically improve risk prediction for complex diseases.
暂无分享,去创建一个
Peter Kraft | Hugues Aschard | Elizabeth W Karlson | Jinbo Chen | Lori B Chibnik | Marilyn C Cornelis | Jinbo Chen | P. Kraft | E. Karlson | L. Chibnik | H. Aschard | M. Cornelis
[1] G. Abecasis,et al. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes , 2010, Genetic epidemiology.
[2] W. Gauderman,et al. Gene-environment interaction in genome-wide association studies. , 2008, American journal of epidemiology.
[3] M. Pepe. The Statistical Evaluation of Medical Tests for Classification and Prediction , 2003 .
[4] M. Pencina,et al. Evaluating the added predictive ability of a new marker: From area under the ROC curve to reclassification and beyond , 2008, Statistics in medicine.
[5] David M. Evans,et al. Two-Stage Two-Locus Models in Genome-Wide Association , 2006, PLoS genetics.
[6] Ewout W Steyerberg,et al. Extensions of net reclassification improvement calculations to measure usefulness of new biomarkers , 2011, Statistics in medicine.
[7] G. Rose. Sick individuals and sick populations. , 2001, International journal of epidemiology.
[8] W. Willett,et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer , 2007, Nature Genetics.
[9] Hon-Cheong So,et al. A Unifying Framework for Evaluating the Predictive Power of Genetic Variants Based on the Level of Heritability Explained , 2010, PLoS genetics.
[10] Chris S. Haley,et al. Epistasis: too often neglected in complex trait studies? , 2004, Nature Reviews Genetics.
[11] R. Wilkins. Polygenes, risk prediction, and targeted prevention of breast cancer. , 2008, The New England journal of medicine.
[12] Peter Kraft,et al. Characterizing Associations and SNP-Environment Interactions for GWAS-Identified Prostate Cancer Risk Markers—Results from BPC3 , 2011, PloS one.
[13] A. Whittemore,et al. Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study , 2010, Breast Cancer Research.
[14] P. Kraft,et al. Cumulative association of 22 genetic variants with seropositive rheumatoid arthritis risk , 2010, Annals of the rheumatic diseases.
[15] C I Amos,et al. Re: Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. , 2009, Journal of the National Cancer Institute.
[16] P. Gregersen,et al. Gene-gene and gene-environment interactions involving HLA-DRB1, PTPN22, and smoking in two subsets of rheumatoid arthritis. , 2007, American journal of human genetics.
[17] Margaret S Pepe,et al. Gauging the performance of SNPs, biomarkers, and clinical factors for predicting risk of breast cancer. , 2008, Journal of the National Cancer Institute.
[18] Beate Ritz,et al. Genome-Wide Gene-Environment Study Identifies Glutamate Receptor Gene GRIN2A as a Parkinson's Disease Modifier Gene via Interaction with Coffee , 2011, PLoS genetics.
[19] Peter Kraft,et al. Gene-environment interactions in genome-wide association studies: a comparative study of tests applied to empirical studies of type 2 diabetes. , 2012, American journal of epidemiology.
[20] E. Demerath,et al. Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children , 2011, PLoS medicine.
[21] M. Gail. Abstract CN07-03: Discriminatory accuracy from Single Nucleotide Polymorphisms in models of absolute breast cancer risk , 2008 .
[22] N. Cook. Use and Misuse of the Receiver Operating Characteristic Curve in Risk Prediction , 2007, Circulation.
[23] 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.
[24] L. Qi,et al. Interactions between genetic factors that predict diabetes and dietary factors that ultimately impact on risk of diabetes , 2010, Current opinion in lipidology.
[25] W. Willett,et al. Moderate alcohol consumption and the risk of breast cancer. , 1987, The New England journal of medicine.
[26] M. Khoury,et al. Genomic profiling to promote a healthy lifestyle: not ready for prime time , 2003, Nature Genetics.
[27] Tianxi Cai,et al. Joint Effects of Common Genetic Variants on the Risk for Type 2 Diabetes in U.S. Men and Women of European Ancestry , 2009, Annals of Internal Medicine.
[28] Michel Eichelbaum,et al. Pharmacogenomics and individualized drug therapy. , 2006, Annual review of medicine.
[29] Peter Kraft,et al. Exploiting Gene-Environment Interaction to Detect Genetic Associations , 2007, Human Heredity.
[30] S. Lewis,et al. Alcohol, ALDH2, and Esophageal Cancer: A Meta-analysis Which Illustrates the Potentials and Limitations of a Mendelian Randomization Approach , 2005, Cancer Epidemiology Biomarkers & Prevention.
[31] Peter Kraft,et al. Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. , 2010, Human molecular genetics.
[32] M. Pirmohamed,et al. Cost-effectiveness analysis of HLA B*5701 genotyping in preventing abacavir hypersensitivity. , 2004, Pharmacogenetics.
[33] Robert M. Plenge,et al. Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis , 2008, PLoS genetics.
[34] M. Gail. Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. , 2008, Journal of the National Cancer Institute.
[35] S. Humphries,et al. Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study , 2010, BMJ : British Medical Journal.
[36] Scott M. Williams,et al. Epistasis and its implications for personal genetics. , 2009, American journal of human genetics.
[37] H. Cordell. Detecting gene–gene interactions that underlie human diseases , 2009, Nature Reviews Genetics.
[38] M S Pepe,et al. Comments on ‘Evaluating the added predictive ability of a new marker: From area under the ROC curve to reclassification and beyond’ by M. J. Pencina et al., Statistics in Medicine (DOI: 10.1002/sim.2929) , 2008, Statistics in medicine.
[39] L. Alfredsson,et al. A gene-environment interaction between smoking and shared epitope genes in HLA-DR provides a high risk of seropositive rheumatoid arthritis. , 2004, Arthritis and rheumatism.
[40] Cornelia M van Duijn,et al. Genome-based prediction of common diseases: advances and prospects. , 2008, Human molecular genetics.
[41] Peter Kraft,et al. Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium. , 2011, Journal of the National Cancer Institute.
[42] Godfrey Fowler,et al. THE STRATEGY OF PREVENTIVE MEDICINE , 1992 .
[43] M. Khoury,et al. An epidemiologic assessment of genomic profiling for measuring susceptibility to common diseases and targeting interventions , 2004, Genetics in Medicine.
[44] Juan Pablo Lewinger,et al. Invited commentary: GE-Whiz! Ratcheting gene-environment studies up to the whole genome and the whole exposome. , 2012, American journal of epidemiology.
[45] Annie E. Hill,et al. Genetic architecture of complex traits: Large phenotypic effects and pervasive epistasis , 2008, Proceedings of the National Academy of Sciences.
[46] J. Bousquet,et al. Effect of 17q21 variants and smoking exposure in early-onset asthma. , 2008, The New England journal of medicine.
[47] Michael E Goddard,et al. which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Multi-locus models of genetic risk of disease , 2009 .
[48] Nilanjan Chatterjee,et al. Common Genetic Variants and Central Adiposity Among Asian‐Indians , 2012, Obesity.
[49] J. Manson,et al. Biomarkers of inflammation and development of rheumatoid arthritis in women from two prospective cohort studies. , 2009, Arthritis and rheumatism.
[50] Nancy R Cook,et al. Association between a literature-based genetic risk score and cardiovascular events in women. , 2010, JAMA.
[51] A. Zlotta. NAT2 Slow Acetylation, GSTM1 Null Genotype, and Risk of Bladder Cancer: Results from the Spanish Bladder Cancer Study and Meta-Analyses , 2006 .
[52] Hongbing Shen,et al. Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations , 2011, Nature Genetics.
[53] Peter Kraft,et al. Gene‐environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop , 2011, Genetic epidemiology.
[54] A. Hofman,et al. American Journal of Epidemiology Practice of Epidemiology Improvement of Risk Prediction by Genomic Profiling: Reclassification Measures versus the Area under the Receiver Operating Characteristic Curve , 2022 .
[55] M. Thun,et al. Performance of Common Genetic Variants in Breast-cancer Risk Models , 2022 .
[56] Mitchell H Gail,et al. On criteria for evaluating models of absolute risk. , 2005, Biostatistics.
[57] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[58] 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.
[59] Kristopher J. Stanya,et al. Genetic variants at 2 q 24 are associated with susceptibility to type 2 diabetes , 2010 .
[60] Kathryn Roeder,et al. Next generation analytic tools for large scale genetic epidemiology studies of complex diseases , 2012, Genetic epidemiology.
[61] F. Grodstein,et al. Do breast-feeding and other reproductive factors influence future risk of rheumatoid arthritis? Results from the Nurses' Health Study. , 2004, Arthritis and rheumatism.
[62] Jaeil Ahn,et al. Testing gene-environment interaction in large-scale case-control association studies: possible choices and comparisons. , 2012, American journal of epidemiology.
[63] David A. Hinds,et al. Assessment of Clinical Validity of a Breast Cancer Risk Model Combining Genetic and Clinical Information , 2010, Journal of the National Cancer Institute.
[64] W. Willett,et al. Multiple loci identified in a genome-wide association study of prostate cancer , 2008, Nature Genetics.
[65] E. Karlson,et al. Smoking intensity, duration, and cessation, and the risk of rheumatoid arthritis in women. , 2006, The American journal of medicine.
[66] D. Thomas,et al. Biological models and statistical interactions: an example from multistage carcinogenesis. , 1981, International journal of epidemiology.
[67] Sander Greenland,et al. The need for reorientation toward cost‐effective prediction: Comments on ‘Evaluating the added predictive ability of a new marker: From area under the ROC curve to reclassification and beyond’ by M. J. Pencina et al., Statistics in Medicine (DOI: 10.1002/sim.2929) , 2008, Statistics in medicine.
[68] W. Willett,et al. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) , 2009, Nature Genetics.