Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
Author(s) -
Jack Bowden,
Fabiola Del Greco M,
Cosetta Minelli,
Qingyuan Zhao,
Debbie A. Lawlor,
Nuala A. Sheehan,
John R. Thompson,
George Davey Smith
Publication year - 2018
Publication title -
international journal of epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.406
H-Index - 208
eISSN - 1464-3685
pISSN - 0300-5771
DOI - 10.1093/ije/dyy258
Subject(s) - mendelian randomization , econometrics , statistics , sample size determination , weighting , mathematics , variance (accounting) , regression , instrumental variable , causality (physics) , computer science , genetic variants , biology , genetics , medicine , physics , accounting , radiology , quantum mechanics , gene , genotype , business
Two-sample summary-data Mendelian randomization (MR) incorporating multiple genetic variants within a meta-analysis framework is a popular technique for assessing causality in epidemiology. If all genetic variants satisfy the instrumental variable (IV) and necessary modelling assumptions, then their individual ratio estimates of causal effect should be homogeneous. Observed heterogeneity signals that one or more of these assumptions could have been violated.
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