Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status
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Bertram Müller-Myhsok | Heribert Schunkert | Damian Gola | Jeannette Erdmann | Inke R König | I. König | H. Schunkert | B. Müller-Myhsok | J. Erdmann | D. Gola
[1] L. Peltonen,et al. A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses , 2010, The Lancet.
[2] Alan M. Kwong,et al. A reference panel of 64,976 haplotypes for genotype imputation , 2015, Nature Genetics.
[3] Eric R. Ziegel,et al. The Elements of Statistical Learning , 2003, Technometrics.
[4] W. März,et al. Rationale and design of the LURIC study--a resource for functional genomics, pharmacogenomics and long-term prognosis of cardiovascular disease. , 2001, Pharmacogenomics.
[5] P. Donnelly,et al. A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies , 2009, PLoS genetics.
[6] Yang I Li,et al. An Expanded View of Complex Traits: From Polygenic to Omnigenic , 2017, Cell.
[7] C. Gieger,et al. Genomewide association analysis of coronary artery disease. , 2007, The New England journal of medicine.
[8] Kurt Hornik,et al. kernlab - An S4 Package for Kernel Methods in R , 2004 .
[9] C. Gieger,et al. Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. , 2011, European heart journal.
[10] D. Levy,et al. Prediction of coronary heart disease using risk factor categories. , 1998, Circulation.
[11] Association study between variants in the fibrinogen gene cluster, fibrinogen levels and hypertension: results from the MONICA/KORA study. , 2009, Thrombosis and haemostasis.
[12] C. Gieger,et al. KORA-gen - Resource for Population Genetics, Controls and a Broad Spectrum of Disease Phenotypes , 2005 .
[13] Stefano Nembrini,et al. The revival of the Gini importance? , 2018, Bioinform..
[14] N. Cook. Statistical evaluation of prognostic versus diagnostic models: beyond the ROC curve. , 2008, Clinical chemistry.
[15] Kurt Hornik,et al. Misc Functions of the Department of Statistics, ProbabilityTheory Group (Formerly: E1071), TU Wien , 2015 .
[16] François Laviolette,et al. Domain-Adversarial Training of Neural Networks , 2015, J. Mach. Learn. Res..
[17] Sarah Lewis,et al. Genetic epidemiology and public health: hope, hype, and future prospects , 2005, The Lancet.
[18] L. Berkman,et al. Genetic susceptibility to death from coronary heart disease in a study of twins. , 1994, The New England journal of medicine.
[19] Alan D. Lopez,et al. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data , 2006, The Lancet.
[20] T. Hansen,et al. A genetic risk score of 45 coronary artery disease risk variants associates with increased risk of myocardial infarction in 6041 Danish individuals. , 2015, Atherosclerosis.
[21] Markus Perola,et al. Genomic prediction of coronary heart disease , 2016, bioRxiv.
[22] J. Danesh,et al. Large-scale association analysis identifies new risk loci for coronary artery disease , 2013 .
[23] Rich Caruana,et al. Predicting good probabilities with supervised learning , 2005, ICML.
[24] A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors , 2017, Scientific Reports.
[25] Andreas Ziegler,et al. ranger: A Fast Implementation of Random Forests for High Dimensional Data in C++ and R , 2015, 1508.04409.
[26] Bernd Bischl,et al. Resampling Methods for Meta-Model Validation with Recommendations for Evolutionary Computation , 2012, Evolutionary Computation.
[27] A. Khera,et al. Genetics of coronary artery disease: discovery, biology and clinical translation , 2017, Nature Reviews Genetics.
[28] Shu Ye,et al. Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults , 2018, Journal of the American College of Cardiology.
[29] T. Thomsen. HeartScore®: a new web-based approach to European cardiovascular disease risk management , 2005, European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology.
[30] M. Keltai,et al. [Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries in a case-control study based on the INTERHEART study]. , 2006, Orvosi hetilap.
[31] S. Yusuf,et al. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study , 2004, The Lancet.
[32] J. Catanese,et al. Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history , 2015, European heart journal.
[33] S. Humphries,et al. Assessment of the clinical utility of adding common single nucleotide polymorphism genetic scores to classical risk factor algorithms in coronary heart disease risk prediction in UK men , 2017, Clinical chemistry and laboratory medicine.
[34] Daniel F. Schwarz,et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3 , 2009, Nature Genetics.
[35] E. DeLong,et al. Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. , 1988, Biometrics.
[36] Bernd Bischl,et al. mlrMBO: A Modular Framework for Model-Based Optimization of Expensive Black-Box Functions , 2017, 1703.03373.
[37] Carson C Chow,et al. Second-generation PLINK: rising to the challenge of larger and richer datasets , 2014, GigaScience.
[38] Mary E. Haas,et al. Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations , 2018, Nature Genetics.
[39] Michael Krawczak,et al. PopGen: Population-Based Recruitment of Patients and Controls for the Analysis of Complex Genotype-Phenotype Relationships , 2006, Public Health Genomics.
[40] J. Friedman. Special Invited Paper-Additive logistic regression: A statistical view of boosting , 2000 .
[41] O. Delaneau,et al. Supplementary Information for ‘ Improved whole chromosome phasing for disease and population genetic studies ’ , 2012 .
[42] Christian Gieger,et al. Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation , 2016, Science Advances.
[43] Trevor Hastie,et al. Regularization Paths for Generalized Linear Models via Coordinate Descent. , 2010, Journal of statistical software.
[44] Andreas Ziegler,et al. Do little interactions get lost in dark random forests? , 2016, BMC Bioinformatics.
[45] Bernd Bischl,et al. mlr: Machine Learning in R , 2016, J. Mach. Learn. Res..
[46] C. Gieger,et al. Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10 p 11 . 23 , 2010 .
[47] K. Taylor,et al. Genome-Wide Association , 2007, Diabetes.
[48] M. Kendall. A NEW MEASURE OF RANK CORRELATION , 1938 .