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

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 GrarupOluf Pedersen, Matias Simons, Leif Groop, Marju Orho-Melander, Mark I. McCarthy, Olle Melander, Peter Rossing, Tuomas O. Kilpeläinen, Torben Hansen

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalDiabetologia
Volume62
Issue number2
Pages (from-to)292-305
Number of pages14
ISSN0012-186X
DOIs
Publication statusPublished - Feb 2019
MoE publication typeA1 Journal article-refereed

Fields of Science

  • Albuminuria
  • Diabetes
  • DKD
  • Exome chip
  • Genetics
  • Genome-wide association study
  • Kidney disease
  • GWAS
  • Rare variant
  • SKAT
  • Type 2 diabetes
  • GENOME-WIDE
  • KIDNEY-DISEASE
  • RISK
  • REVEALS
  • LOCI
  • METAANALYSIS
  • PROTECTION
  • RECEPTORS
  • DISCOVERY
  • FRAMEWORK
  • 3121 Internal medicine
  • 3111 Biomedicine
  • 1184 Genetics, developmental biology, physiology

Cite this

Ahluwalia, T. S., Schulz, C-A., Waage, J., Skaaby, T., Sandholm, N., van Zuydam, N., Charmet, R., Bork-Jensen, J., Almgren, P., Thuesen, B. H., Bedin, M., Brandslund, I., Christensen, C. K., Linneberg, A., Ahlqvist, E., Groop, P-H., Hadjadj, S., Tregouet, D-A., Jorgensen, M. E., ... Hansen, T. (2019). 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. Diabetologia, 62(2), 292-305. https://doi.org/10.1007/s00125-018-4783-z