1. Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation. (1st June 2017) Authors: Lieve, Krystien V.; Verkerk, Arie O.; Podliesna, Svitlana; van der Werf, Christian; Tanck, Michael W.; Hofman, Nynke; van Bergen, Paul F.; Beekman, Leander; Bezzina, Connie R.; Wilde, Arthur A.M.; Lodder, Elisabeth M. Journal: International journal of cardiology Issue: Volume 236(2017) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Pacing Discovery: G-Protein β Subunit Mutations in Sinus Node Dysfunction. Issue 10 (12th May 2017) Authors: Lodder, Elisabeth M.; Verkerk, Arie O.; Bezzina, Connie R. Journal: Circulation research Issue: Volume 120:Issue 10(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease–Causing Mutation. Issue 7 (24th July 2017) Authors: Veerman, Christiaan C.; Mengarelli, Isabella; Lodder, Elisabeth M.; Kosmidis, Georgios; Bellin, Milena; Zhang, Miao; Dittmann, Sven; Guan, Kaomei; Wilde, Arthur A. M.; Schulze‐Bahr, Eric; Greber, Boris; Bezzina, Connie R.; Verkerk, Arie O. Journal: Journal of the American Heart Association Issue: Volume 6:Issue 7(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease–Causing Mutation. Issue 7 (July 2017) Authors: Veerman, Christiaan C.; Mengarelli, Isabella; Lodder, Elisabeth M.; Kosmidis, Georgios; Bellin, Milena; Zhang, Miao; Dittmann, Sven; Guan, Kaomei; Wilde, Arthur A. M.; Schulze‐Bahr, Eric; Greber, Boris; Bezzina, Connie R.; Verkerk, Arie O. Journal: Journal of the American Heart Association Issue: Volume 6:Issue 7(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity. Issue 5 (18th August 2017) Authors: Veerman, Christiaan C.; Podliesna, Svitlana; Tadros, Rafik; Lodder, Elisabeth M.; Mengarelli, Isabella; de Jonge, Berend; Beekman, Leander; Barc, Julien; Wilders, Ronald; Wilde, Arthur A.M.; Boukens, Bastiaan J.; Coronel, Ruben; Verkerk, Arie O.; Remme, Carol Ann; Bezzina, Connie R. Journal: Circulation research Issue: Volume 121:Issue 5(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗