Mendelian randomization: a novel approach for the prediction of adverse drug events and drug repurposing opportunities
暂无分享,去创建一个
Neil M Davies | Richard M Martin | George Davey Smith | Venexia M Walker | G. Davey Smith | N. Davies | Richard M. Martin | V. Walker
[1] J. Rassen,et al. Confounding Control in Healthcare Database Research: Challenges and Potential Approaches , 2010, Medical care.
[2] S. Gottlieb,et al. US consumer groups allege misleading drug claims , 2001, BMJ : British Medical Journal.
[3] J. Thompson,et al. Beyond Mendelian randomization: how to interpret evidence of shared genetic predictors , 2016, Journal of clinical epidemiology.
[4] Sonia S Anand,et al. Emerging risk factors for atherosclerotic vascular disease: a critical review of the evidence. , 2003, JAMA.
[5] F. Rosendaal,et al. Fibrinogen polymorphisms are not associated with the risk of myocardial infarction , 2000, British journal of haematology.
[6] Hashem A. Shihab,et al. MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations , 2016, bioRxiv.
[7] G. Davey Smith,et al. Mendelian randomization: genetic anchors for causal inference in epidemiological studies , 2014, Human molecular genetics.
[8] Yasuo Ohashi,et al. Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials , 2010, The Lancet.
[9] Tanya M. Teslovich,et al. Discovery and refinement of loci associated with lipid levels , 2013, Nature Genetics.
[10] Simon M Lin,et al. Opportunities for drug repositioning from phenome-wide association studies , 2015, Nature Biotechnology.
[11] P Ryan,et al. Novel Data‐Mining Methodologies for Adverse Drug Event Discovery and Analysis , 2012, Clinical pharmacology and therapeutics.
[12] Jennifer G. Robinson,et al. Safety of Very Low Low-Density Lipoprotein Cholesterol Levels With Alirocumab: Pooled Data From Randomized Trials. , 2017, Journal of the American College of Cardiology.
[13] A. M. Lefer,et al. Vascular effects of HMG CoA-reductase inhibitors (statins) unrelated to cholesterol lowering: new concepts for cardiovascular disease. , 2001, Cardiovascular research.
[14] A. Hofman,et al. Elevated plasma fibrinogen: cause or consequence of cardiovascular disease? , 1998, Arteriosclerosis, thrombosis, and vascular biology.
[15] Debbie A Lawlor,et al. Triangulation in aetiological epidemiology , 2016, International journal of epidemiology.
[16] D. Roden,et al. Phenome-Wide Association Studies as a Tool to Advance Precision Medicine. , 2016, Annual review of genomics and human genetics.
[17] Diana Petitti,et al. Commentary: hormone replacement therapy and coronary heart disease: four lessons. , 2004, International journal of epidemiology.
[18] S. Ebrahim,et al. 'Mendelian randomization': can genetic epidemiology contribute to understanding environmental determinants of disease? , 2003, International journal of epidemiology.
[19] G. Davey Smith,et al. Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression , 2015, International journal of epidemiology.
[20] Masayoshi Hashimoto,et al. Cerivastatin, a hydroxymethylglutaryl coenzyme A reductase inhibitor, improves endothelial function in elderly diabetic patients within 3 days , 2002 .
[21] Katherine M. Siewert,et al. Serum calcium and risk of migraine: a Mendelian randomization study , 2016, Human molecular genetics.
[22] Peter Sandercock,et al. Interpretation of the evidence for the efficacy and safety of statin therapy , 2016, The Lancet.
[23] G. Smith,et al. Mendelian randomization in cardiometabolic disease: challenges in evaluating causality , 2017, Nature Reviews Cardiology.
[24] L. Cardon,et al. Use of genome-wide association studies for drug repositioning , 2012, Nature Biotechnology.
[25] K I Kaitin,et al. Deconstructing the Drug Development Process: The New Face of Innovation , 2010, Clinical pharmacology and therapeutics.
[26] S. Humphries,et al. A common mutation (G-455--> A) in the beta-fibrinogen promoter is an independent predictor of plasma fibrinogen, but not of ischemic heart disease. A study of 9,127 individuals based on the Copenhagen City Heart Study. , 1997, Journal of Clinical Investigation.
[27] James P. Wilson,et al. Rhabdomyolysis and HMG-CoA Reductase Inhibitors , 2001, The Annals of pharmacotherapy.
[28] Bertram Pitt,et al. Withdrawal of cerivastatin from the world market , 2001, Current controlled trials in cardiovascular medicine.
[29] S Shapiro,et al. Confounding by indication? , 1997, Epidemiology.
[30] U. Laufs,et al. Rapid effects on vascular function after initiation and withdrawal of atorvastatin in healthy, normocholesterolemic men. , 2001, The American journal of cardiology.
[31] John Spertus,et al. Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study , 2012, The Lancet.
[32] G. Davey Smith,et al. Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator , 2016, Genetic epidemiology.
[33] R. Laaksonen,et al. Low-density lipoprotein-independent effects of statins. , 1999, Current opinion in lipidology.
[34] MasayoshiHashimoto,et al. Cerivastatin, a Hydroxymethylglutaryl Coenzyme A Reductase Inhibitor, Improves Endothelial Function in Elderly Diabetic Patients Within 3 Days , 2002 .
[35] Graves Ej,et al. Detailed diagnoses and procedures, National Hospital Discharge Survey, 1994. , 1997, Vital and health statistics. Series 13, Data from the National Health Survey.
[36] T. A. Jacobson,et al. The broad spectrum of statin myopathy: from myalgia to rhabdomyolysis , 2007, Current opinion in lipidology.
[37] Ruth Pfeiffer,et al. Mendelian Randomization: How It Can—and Cannot—Help Confirm Causal Relations between Nutrition and Cancer , 2009, Cancer Prevention Research.
[38] R. Hegele,et al. Narrative Review: Statin-Related Myopathy , 2009, Annals of Internal Medicine.
[39] A. Gaggl,et al. Summaries , 2011, Mund-, Kiefer- und Gesichtschirurgie.
[40] Richard Platt,et al. Incidence of hospitalized rhabdomyolysis in patients treated with lipid-lowering drugs. , 2004, JAMA.
[41] G. Leung,et al. Genetically predicted 17beta-estradiol and cardiovascular risk factors in women: a Mendelian randomization analysis using young women in Hong Kong and older women in the Guangzhou Biobank Cohort Study. , 2016, Annals of epidemiology.
[42] John P. Overington,et al. The druggable genome and support for target identification and validation in drug development , 2016, Science Translational Medicine.
[43] A. Daly,et al. Genome-wide association studies in pharmacogenomics , 2010, Nature Reviews Genetics.
[44] R. Brook,et al. Effect of naturally random allocation to lower low-density lipoprotein cholesterol on the risk of coronary heart disease mediated by polymorphisms in NPC1L1, HMGCR, or both: a 2 × 2 factorial Mendelian randomization study. , 2015, Journal of the American College of Cardiology.
[45] Sarah Parish,et al. Fibrinogen and coronary heart disease: test of causality by 'Mendelian randomization'. , 2006, International journal of epidemiology.
[46] Jun S. Liu,et al. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans , 2015, Science.
[47] Samuel E. Jones,et al. GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology , 2018, American journal of human genetics.
[48] Patrick C Waller,et al. A model for the future conduct of pharmacovigilance , 2003, Pharmacoepidemiology and drug safety.
[49] Szilard Voros,et al. Variation in PCSK9 and HMGCR and Risk of Cardiovascular Disease and Diabetes. , 2016, The New England journal of medicine.
[50] Jennie Chang,et al. Cerivastatin and reports of fatal rhabdomyolysis. , 2002, The New England journal of medicine.
[51] Anne Corbett,et al. Drug repositioning in Alzheimer's disease. , 2015, Frontiers in bioscience.
[52] G. Davey Smith,et al. Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges , 2017, bioRxiv.
[53] G. Colditz,et al. Estrogen replacement therapy and coronary heart disease: A quantitative assessment of the epidemiologic evidence☆☆☆ , 1991 .
[54] R. Wanders,et al. Rhabdomyolysis: a review of the literature , 1993, Clinical Neurology and Neurosurgery.
[55] W. Koenig. Fibrinogen and coronary risk , 1999, Current cardiology reports.
[56] Hynek Pikhart,et al. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study , 2017, The lancet. Diabetes & endocrinology.
[57] Hynek Pikhart,et al. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials , 2015, The Lancet.
[58] George Davey Smith,et al. Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology , 2008, Statistics in medicine.
[59] Vladimir V Poroikov,et al. In silico assessment of adverse drug reactions and associated mechanisms. , 2016, Drug discovery today.
[60] Dolores Corella,et al. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans , 2008, Nature Genetics.
[61] M. Reilly,et al. PCSK9 is a critical regulator of the innate immune response and septic shock outcome , 2014, Science Translational Medicine.
[62] Matthew R. Nelson,et al. The genetics of drug efficacy: opportunities and challenges , 2016, Nature Reviews Genetics.
[63] A. Keech,et al. Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease , 2017, The New England journal of medicine.
[64] A. Daly. Using genome-wide association studies to identify genes important in serious adverse drug reactions. , 2012, Annual review of pharmacology and toxicology.
[65] B. Gillum,et al. Detailed diagnoses and procedures, National Hospital Discharge Survey, 1995. , 1997, Vital and health statistics. Series 13, Data from the National Health Survey.
[66] N. Timpson,et al. MR-PheWAS: hypothesis prioritization among potential causal effects of body mass index on many outcomes, using Mendelian randomization , 2015, Scientific Reports.
[67] Manuel A. R. Ferreira,et al. Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis , 2015, The lancet. Diabetes & endocrinology.
[68] Dana C. Crawford,et al. Unravelling the human genome–phenome relationship using phenome-wide association studies , 2016, Nature Reviews Genetics.
[69] S. Ebrahim,et al. Mendelian randomization: prospects, potentials, and limitations. , 2004, International journal of epidemiology.
[70] L. Lerman,et al. Statin effects beyond lipid lowering--are they clinically relevant? , 2003, European heart journal.
[71] T. Ashburn,et al. Drug repositioning: identifying and developing new uses for existing drugs , 2004, Nature Reviews Drug Discovery.
[72] Brian A Ference,et al. Association Between Lowering LDL-C and Cardiovascular Risk Reduction Among Different Therapeutic Interventions: A Systematic Review and Meta-analysis. , 2016, JAMA.
[73] Sara M. Willems,et al. Association Between Low-Density Lipoprotein Cholesterol-Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis. , 2016, JAMA.
[74] S. Bandinelli,et al. Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults. , 2014, Cytokine.
[75] A. Hoes,et al. Quantitative assessment of unobserved confounding is mandatory in nonrandomized intervention studies. , 2009, Journal of clinical epidemiology.
[76] D. Lawlor,et al. Clustered Environments and Randomized Genes: A Fundamental Distinction between Conventional and Genetic Epidemiology , 2007, PLoS medicine.
[77] J. Varon,et al. Beyond muscle destruction: a systematic review of rhabdomyolysis for clinical practice , 2016, Critical Care.
[78] G. Smith. Use of genetic markers and gene-diet interactions for interrogating population-level causal influences of diet on health , 2011, Genes & Nutrition.
[79] G. Lip,et al. Fibrinogen: biochemistry, epidemiology and determinants. , 2003, QJM : monthly journal of the Association of Physicians.
[80] Shah Ebrahim,et al. Socioeconomic position and hormone replacement therapy use: explaining the discrepancy in evidence from observational and randomized controlled trials. , 2004, American journal of public health.
[81] G. Di Minno,et al. Measuring plasma fibrinogen to predict stroke and myocardial infarction: an update. , 1999, Arteriosclerosis, thrombosis, and vascular biology.
[82] S. Kathiresan,et al. Leveraging human genetics to guide drug target discovery. , 2017, Trends in cardiovascular medicine.
[83] C. Stehouwer,et al. Association of common gene variants in glucokinase regulatory protein with cardiorenal disease: A systematic review and meta-analysis , 2018, PloS one.
[84] Shah Ebrahim,et al. Does Elevated Plasma Fibrinogen Increase the Risk of Coronary Heart Disease?: Evidence from a Meta-Analysis of Genetic Association Studies , 2005, Arteriosclerosis, thrombosis, and vascular biology.
[85] G A Colditz,et al. Estrogen replacement therapy and coronary heart disease: a quantitative assessment of the epidemiologic evidence. , 2004, Preventive medicine.
[86] Janice M. Reichert,et al. A guide to drug discovery: Trends in development and approval times for new therapeutics in the United States , 2003, Nature Reviews Drug Discovery.