Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease. (2018)
Attributed to:
Mendelian randomization to hypothesis-free causal inference
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddy210
PubMed Identifier: 29893838
Publication URI: http://europepmc.org/abstract/MED/29893838
Type: Journal Article/Review
Volume: 27
Parent Publication: Human molecular genetics
Issue: 18
ISSN: 0964-6906