Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes

por Charmet, Romain, Duffy, Seamus, Keshavarzi, Sareh, Gyorgy, Beata, Marre, Michel, Rossing, Peter, McKnight, Amy Jayne, Maxwell, Alexander P., Ahluwalia, Tarun veer Singh, Paterson, Andrew D., Trégouët, David-Alexandre, Hadjadj, Samy
Publicado 2018

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

por Ahluwalia, Tarunveer S., Schulz, Christina-Alexandra, Waage, Johannes, Skaaby, Tea, Sandholm, Niina, van Zuydam, Natalie, Charmet, Romain, Bork-Jensen, Jette, Almgren, Peter, Thuesen, Betina H., Bedin, Mathilda, Brandslund, Ivan, Christensen, Cramer K., Linneberg, Allan, Ahlqvist, Emma, Groop, Per-Henrik, Hadjadj, Samy, Tregouet, David-Alexandre, Jørgensen, Marit E., Grarup, Niels, Pedersen, Oluf, Simons, Matias, Groop, Leif, Orho-Melander, Marju, McCarthy, Mark I., Melander, Olle, Rossing, Peter, Kilpeläinen, Tuomas O., Hansen, Torben
Publicado 2018