Using published data in Mendelian randomization: a blueprint for efficient identification of causal risk factors.

Eur J Epidemiol · 2015 · PMC4516908 · PMID 25773750

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nominally significantno p-value reported

The estimate using all the genetic variants is more precise than the estimate using only a subset of variants, even though the additional variants are not associated with calcium at nominally significant levels.

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