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 articleResearchpeer-review

Tarunveer S. Ahluwalia, 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, Allan Linneberg, Emma Ahlqvist, Per-Henrik Groop, Samy Hadjadj, David-Alexandre Tregouet, Marit E. Jorgensen, Niels Grarup & 9 more Oluf Pedersen, Matias Simons, Leif Groop, Marju Orho-Melander, Mark I. McCarthy, Olle Melander, Peter Rossing, Tuomas O. Kilpelainen, Torben Hansen

Original languageEnglish
JournalDiabetologia
Volume62
Issue number2
Pages (from-to)292-305
ISSN0012-186X
DOIs
Publication statusPublished - 2019

    Research areas

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

ID: 214686242