A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria

Research output: Contribution to journalJournal articlepeer-review

  • Christina-Alexandra Schulz
  • Johannes Waage
  • Tea Skaaby
  • Niina Sandholm
  • Natalie van Zuydam
  • Romain Charmet
  • Jette Bork-Jensen
  • Peter Almgren
  • Betina H. Thuesen
  • Mathilda Bedin
  • Ivan Brandslund
  • Cramer K. Christensen
  • Emma Ahlqvist
  • Per-Henrik Groop
  • Samy Hadjadj
  • David-Alexandre Tregouet
  • Marit E. Jorgensen
  • Matias Simons
  • Leif Groop
  • Marju Orho-Melander
  • Mark I. McCarthy
  • Olle Melander
Original languageEnglish
Issue number2
Pages (from-to)292-305
Publication statusPublished - 2019

    Research areas

  • Albuminuria, Diabetes, DKD, Exome chip, Genetics, Genome-wide association study, Kidney disease, GWAS, Rare variant, SKAT, Type 2 diabetes

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ID: 214686242