Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Save this search Download search results Subscribe to news feed Your filters: cql: author="Schepers, Dorien" or (type any "bookEditor journalEditor issueEditor" and editor="Scheper... Add to list Journal Article A1 open access Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia Nikhita Ajit Bolar, Christelle Golzio, Martina Živná, Gaëlle Hayot, CHRISTINE VAN HEMELRIJK (UGent) , Dorien Schepers, Geert Vandeweyer, Alexander Hoischen, Jeroen R Huyghe, Ann Raes (UGent) , et al. (2016) AMERICAN JOURNAL OF HUMAN GENETICS. 99(1). p.174-187 Add to list Journal Article A2 open access Lessons learned from the intersection of two frequent monogenic disorders : the Marfan syndrome and autosomal dominant polycystic kidney disease Dorien Schepers, Stéphanie Dautricourt, Lauranne De Decker, Ann Raes (UGent) , Lut Van Laer and Bart Loeys (UGent) (2013) PROCEEDINGS OF THE BELGIAN ROYAL ACADEMIES OF MEDICINE. 2. p.179-197