Nature Communications (Jul 2021)

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

  • Kira J. Stanzick,
  • Yong Li,
  • Pascal Schlosser,
  • Mathias Gorski,
  • Matthias Wuttke,
  • Laurent F. Thomas,
  • Humaira Rasheed,
  • Bryce X. Rowan,
  • Sarah E. Graham,
  • Brett R. Vanderweff,
  • Snehal B. Patil,
  • VA Million Veteran Program,
  • Cassiane Robinson-Cohen,
  • John M. Gaziano,
  • Christopher J. O’Donnell,
  • Cristen J. Willer,
  • Stein Hallan,
  • Bjørn Olav Åsvold,
  • Andre Gessner,
  • Adriana M. Hung,
  • Cristian Pattaro,
  • Anna Köttgen,
  • Klaus J. Stark,
  • Iris M. Heid,
  • Thomas W. Winkler

DOI
https://doi.org/10.1038/s41467-021-24491-0
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 17

Abstract

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Identifying causal variants and genes in genome-wide association studies remains a challenge, an issue that is ameliorated with larger sample sizes. Here the authors meta-analyze kidney function genome-wide association studies to identify new loci and fine-map loci to home in on variants and genes involved in kidney function.