Ghent University Academic Bibliography

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Your filters: cql: author="Schepers, Dorien" or (type exact bookEditor and editor="Schepers, Dorien")

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Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes

Aleksandra Nijak, Eline Simons, Bert Vandendriessche, Dieter Van de Sande, Erik Fransen, Ewa Sieliwonczyk, Ilse Van Gucht, Emeline Van Craenenbroeck, Johan Saenen, Hein Heidbuchel, et al.

(2022) BIOLOGY OPEN. 11(2).
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iPSC-cardiomyocyte models of Brugada syndrome : achievements, challenges and future perspectives

Aleksandra Nijak, Johan Saenen, Alain J Labro (UGent) , Dorien Schepers, Bart L. Loeys and Maaike Alaerts

(2021) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 22(6).
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Compound heterozygous SCN5A mutations in severe sodium channelopathy with Brugada syndrome : a case report

Aleksandra Nijak, Alain J Labro (UGent) , Hans De Wilde (UGent) , Wendy Dewals, Steve Peigneur, Jan Tytgat, Dirk Snyders, Ewa Sieliwonczyk, Eline Simons, Emeline Van Craenenbroeck, et al.

(2020) FRONTIERS IN CARDIOVASCULAR MEDICINE. 7.
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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
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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

Academic Bibliography

Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes

iPSC-cardiomyocyte models of Brugada syndrome : achievements, challenges and future perspectives

Compound heterozygous SCN5A mutations in severe sodium channelopathy with Brugada syndrome : a case report

Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia

Lessons learned from the intersection of two frequent monogenic disorders : the Marfan syndrome and autosomal dominant polycystic kidney disease

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