Using multiple genetic variants as instrumental variables for modifiable risk factors.
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MR-PheWAS: hypothesis prioritization among potential causal effects of body mass index on many outcomes, using Mendelian randomizationPolygenic EpidemiologyPregnancy diet and associated outcomes in the Avon Longitudinal Study of Parents and ChildrenPoverty, Pregnancy, and Birth Outcomes: A Study of the Earned Income Tax CreditPleiotropy in complex traits: challenges and strategiesAssessing causality in the association between child adiposity and physical activity levels: a Mendelian randomization analysisAssessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization AnalysisThe role of adiposity in cardiometabolic traits: a Mendelian randomization analysisSerum iron levels and the risk of Parkinson disease: a Mendelian randomization study.Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohortsSerum uric acid and adiposity: deciphering causality using a bidirectional Mendelian randomization approachEvaluation of genetic markers as instruments for Mendelian randomization studies on vitamin DThe effect of elevated body mass index on ischemic heart disease risk: causal estimates from a Mendelian randomisation approachPlasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyMendelian Randomization as an Approach to Assess Causality Using Observational Data.Mendelian randomization of blood lipids for coronary heart disease.Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis.Mendelian randomization analysis with multiple genetic variants using summarized data.Detecting pleiotropy in Mendelian randomisation studies with summary data and a continuous outcome.Mendelian randomization analysis of a time-varying exposure for binary disease outcomes using functional data analysis methods.Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degenerationEffect of handgrip on coronary artery disease and myocardial infarction: a Mendelian randomization study.Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation studyApolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysisCausal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study.Methods for meta-analysis of individual participant data from Mendelian randomisation studies with binary outcomes.Obesity and risk of esophageal adenocarcinoma and Barrett's esophagus: a Mendelian randomization study.Mendelian randomization supports causality between maternal hyperglycemia and epigenetic regulation of leptin gene in newborns.Vitamin D status, filaggrin genotype, and cardiovascular risk factors: a Mendelian randomization approach.Model selection approach suggests causal association between 25-hydroxyvitamin D and colorectal cancerTesting for non-linear causal effects using a binary genotype in a Mendelian randomization study: application to alcohol and cardiovascular traits.Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case-control studyThe many weak instruments problem and Mendelian randomization.Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?A Mendelian randomization study of the effect of type-2 diabetes on coronary heart disease.Evaluation of an association between plasma total homocysteine and schizophrenia by a Mendelian randomization analysis.Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk.Contemporary Considerations for Constructing a Genetic Risk Score: An Empirical Approach.Credible Mendelian randomization studies: approaches for evaluating the instrumental variable assumptionsAdiposity as a cause of cardiovascular disease: a Mendelian randomization study.
P2860
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P2860
Using multiple genetic variants as instrumental variables for modifiable risk factors.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Using multiple genetic variants as instrumental variables for modifiable risk factors.
@en
Using multiple genetic variants as instrumental variables for modifiable risk factors.
@en-gb
type
label
Using multiple genetic variants as instrumental variables for modifiable risk factors.
@en
Using multiple genetic variants as instrumental variables for modifiable risk factors.
@en-gb
prefLabel
Using multiple genetic variants as instrumental variables for modifiable risk factors.
@en
Using multiple genetic variants as instrumental variables for modifiable risk factors.
@en-gb
P2860
P50
P356
P1476
Using multiple genetic variants as instrumental variables for modifiable risk factors.
@en
P2093
Jonathan A C Sterne
P2860
P304
P356
10.1177/0962280210394459
P50
P577
2011-01-07T00:00:00Z