1. A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. (April 2020) Authors: Brodehl, Andreas; Weiss, Jürgen; Debus, Jana Davina; Stanasiuk, Caroline; Klauke, Bärbel; Deutsch, Marcus André; Fox, Henrik; Bax, Jördis; Ebbinghaus, Hans; Gärtner, Anna; Tiesmeier, Jens; Laser, Thorsten; Peterschröder, Andreas; Gerull, Brenda; Gummert, Jan; Paluszkiewicz, Lech; Milting, Hendrik Journal: Journal of molecular and cellular cardiology Issue: Volume 141(2020) Page Start: 17 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Antisense‐mediated exon skipping: a therapeutic strategy for titin‐based dilated cardiomyopathy. Issue 5 (10th March 2015) Authors: Gramlich, Michael; Pane, Luna Simona; Zhou, Qifeng; Chen, Zhifen; Murgia, Marta; Schötterl, Sonja; Goedel, Alexander; Metzger, Katja; Brade, Thomas; Parrotta, Elvira; Schaller, Martin; Gerull, Brenda; Thierfelder, Ludwig; Aartsma‐Rus, Annemieke; Labeit, Siegfried; Atherton, John J; McGaughran, Ju... Journal: EMBO molecular medicine Issue: Volume 7:Issue 5(2015:May) Page Start: 562 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype. Issue 8 (24th April 2019) Authors: Kolokotronis, Konstantinos; Kühnisch, Jirko; Klopocki, Eva; Dartsch, Josephine; Rost, Simone; Huculak, Cathleen; Mearini, Giulia; Störk, Stefan; Carrier, Lucie; Klaassen, Sabine; Gerull, Brenda Journal: Human mutation Issue: Volume 40:Issue 8(2019) Page Start: 1101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry. (September 2016) Authors: Steinberg, Christian; Padfield, Gareth J.; Champagne, Jean; Sanatani, Shubhayan; Angaran, Paul; Andrade, Jason G.; Roberts, Jason D.; Healey, Jeffrey S.; Chauhan, Vijay S.; Birnie, David H.; Janzen, Mikyla; Gerull, Brenda; Klein, George J.; Leather, Richard; Simpson, Christopher S.; Seifer, Colet... Journal: Circulation Issue: Volume 9:Number 9(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect. (February 2016) Authors: Brodehl, Andreas; Dieding, Mareike; Biere, Niklas; Unger, Andreas; Klauke, Bärbel; Walhorn, Volker; Gummert, Jan; Schulz, Uwe; Linke, Wolfgang A.; Gerull, Brenda; Vorgert, Matthias; Anselmetti, Dario; Milting, Hendrik Journal: Journal of molecular and cellular cardiology Issue: Volume 91(2016:Feb.) Page Start: 207 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic Association Study in Multigenerational Kindreds With Vasovagal Syncope: Evidence for Involvement of Sex-Specific Serotonin Signaling. (January 2019) Authors: Sheldon, Robert; Rose, M. Sarah; Ritchie, Debbie; Martens, Kristina; Maxey, Connor; Jagers, Jennie; Parboosingh, Jillian; Gerull, Brenda Journal: Circulation Issue: Volume 12:Number 1(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry). (June 2017) Authors: Mellor, Greg; Laksman, Zachary W.M.; Tadros, Rafik; Roberts, Jason D.; Gerull, Brenda; Simpson, Christopher S.; Klein, George J.; Champagne, Jean; Talajic, Mario; Gardner, Martin; Steinberg, Christian; Arbour, Laura; Birnie, David H.; Angaran, Paul; Leather, Richard; Sanatani, Shubhayan; Chauhan,... Journal: Circulation Issue: Volume 10:Number 3(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Immuno-metabolic interfaces in cardiac disease and failure. Issue 1 (4th February 2021) Authors: Bertero, Edoardo; Dudek, Jan; Cochain, Clement; Delgobo, Murilo; Ramos, Gustavo; Gerull, Brenda; Higuchi, Takahiro; Vaeth, Martin; Zernecke, Alma; Frantz, Stefan; Hofmann, Ulrich; Maack, Christoph Journal: Cardiovascular research Issue: Volume 118:Issue 1(2022) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?. (August 2017) Authors: Roberts, Jason D.; Krahn, Andrew D.; Ackerman, Michael J.; Rohatgi, Ram K.; Moss, Arthur J.; Nazer, Babak; Tadros, Rafik; Gerull, Brenda; Sanatani, Shubhayan; Wijeyeratne, Yanushi D.; Baruteau, Alban-Elouen; Muir, Alison R.; Pang, Benjamin; Cadrin-Tourigny, Julia; Talajic, Mario; Rivard, Lena; Te... Journal: Circulation Issue: Volume 10:Number 8(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy. Issue 2 (4th January 2023) Authors: Chen, Ruping; Buchmann, Simone; Kroth, Amos; Arias-Loza, Anahi-Paula; Kohlhaas, Michael; Wagner, Nicole; Grüner, Gianna; Nickel, Alexander; Cirnu, Alexandra; Williams, Tatjana; Maack, Christoph; Ergün, Süleyman; Frantz, Stefan; Gerull, Brenda Journal: Circulation research Issue: Volume 132:Issue 2(2023) Page Start: e43 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗