📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases. (2023)

First Author: Yuan K
Attributed to:  UK Biobank (core renewal) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2023.01.07.23284293

PubMed Identifier: 36711496

Publication URI: http://europepmc.org/abstract/MED/36711496

Type: Journal Article/Review

Parent Publication: medRxiv : the preprint server for health sciences