A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes - Publications

Novo Nordisk Foundation
Center for Basic Metabolic Research

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

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A novel rareCUBNvariant and three additional genes identifiedin Europeans with and without diabetes: results from an exome-wideassociation study of albuminuria
Final published version, 1.58 MB, PDF document

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 language	English
Journal	Diabetologia
Volume	62
Issue number	2
Pages (from-to)	292-305
ISSN	0012-186X
DOIs	https://doi.org/10.1007/s00125-018-4783-z
Publication status	Published - 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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