Anna Gaertner (Anna Gaertner-Rommel, Anna Gärtner)

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 10

Top Topics

Top Venues

International journal of molecular sciences

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Anna Gaertner, Lidia Burr, Baerbel Klauke, Andreas Brodehl, Kai Thorsten Laser, Karin Klingel, Jens Tiesmeier, Uwe Schulz, Edzard Zu Knyphausen, Jan Gummert, Andreas Brodehl
Compound Heterozygous FKTN Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern. International journal of molecular sciences 23 (12) (2022)
Franziska Seidel, Kai Thorsten Laser, Karin Klingel, Josephine Dartsch, Simon Theisen, Thomas Pickardt, Manuel Holtgrewe, Anna Gaertner, Felix Berger, Dieter Beule, Andreas Brodehl, Stephan Schubert, Sabine Klaassen, Jirko Kühnisch
Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis-Further Impact of Heterozygous Immune Disorder Gene Variants? Journal of cardiovascular development and disease 9 (7) (2022)
Daniel Reichart, Eric Lars-Helge Lindberg, Henrike Maatz, Antonio M A Miranda, Anissa Viveiros, Nikolay Shvetsov, Anna Gaertner, Emily R Nadelmann, Michael Lee, Kazumasa Kanemaru, Jorge Ruiz-Orera, Viktoria Strohmenger, Daniel M DeLaughter, Giannino Patone, Hao Zhang, Andrew Woehler, Christoph Lippert, Yuri Kim, Eleonora Adami, Joshua M Gorham, Sam N Barnett, Kemar J Brown, Rachel J Buchan, Rasheda A Chowdhury, Chrystalla Constantinou, James Cranley, Leanne E Felkin, Henrik Fox, Ahla Ghauri, Jan F Gummert, Masatoshi Kanda, Ruoyan Li, Lukas Mach, Barbara McDonough, Sara Samari, Farnoush Shahriaran, Clarence Yapp, Caroline Stanasiuk, Pantazis I Theotokis, Fabian Joachim Theis, Antoon van den Bogaerdt, Hiroko Wakimoto, James Simon Ware, Catherine L Worth, Paul J R Barton, Young-Ae Lee, Sarah A Teichmann, Andreas Brodehl, Michela Noseda, Gavin Y Oudit, Matthias Heinig, Jonathan G Seidman, Norbert Hübner, Christine E Seidman
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies. Science (New York, N.Y.) 377 (6606) (2022)
Roua Hassoun, Heidi Budde, Hans Georg Mannherz, Mária Lódi, Setsuko Fujita-Becker, Kai Thorsten Laser, Anna Gaertner, Karin Klingel, Desirée Möhner, Robert Stehle, Innas Sultana, Thomas Schaaf, Mario Majchrzak, Verena Krause, Christian Herrmann, Marc M Nowaczyk, Andreas Mügge, Gabriele Pfitzer, Rasmus R Schröder, Nazha Hamdani, Hendrik Milting, Kornelia Jaquet, Diana Cimiotti
De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents. International journal of molecular sciences 22 (17) (2021)
Andreas Brodehl, Carsten Hain, Franziska Flottmann, Sandra Ratnavadivel, Anna Gaertner, Bärbel Klauke, Jörn Kalinowski, Hermann Köerperich, Jan Gummert, Lech Paluszkiewicz, Marcus-André Deutsch, Andreas Brodehl
The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3. Biomedicines 9 (10) (2021)
Anna Gaertner, Julia Bloebaum, Andreas Brodehl, Baerbel Klauke, Katharina Sielemann, Astrid Kassner, Henrik Fox, Michiel Morshuis, Jens Tiesmeier, Uwe Schulz, Ralph Knoell, Jan Gummert, Hendrik Milting
The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy. Genes 12 (6) (2021)
Andrey Fomin, Anna Gaertner, Lukas Cyganek, Malte Tiburcy, Izabela Tuleta, Luisa Wellers, Lina Folsche, Anastasia J Hobbach, Marion von Frieling-Salewsky, Andreas Unger, Anna Hucke, Franziska Koser, Astrid Kassner, Katharina Frey, Katrin Streckfuß-Bömeke, Gerd Hasenfuss, Alexander Goedel, Karl-Ludwig Laugwitz, Alessandra Moretti, Jan F Gummert, Cristobal G Dos Remedios, Holger Reinecke, Ralph Knoell, Sebastiaan van Heesch, Norbert Hübner, Wolfgram-Hubertus Zimmermann, Andreas Brodehl, Wolfgang A Linke
Truncated titin proteins and titin haploinsufficiency are targets for functional recovery in human cardiomyopathy due to TTN mutations. Science translational medicine 13 (618) (2021)
Anna Gaertner, Baerbel Klauke, Elina Felski, Astrid Kassner, Andreas Brodehl, Désirée Gerdes, Caroline Stanasiuk, Hans Ebbinghaus, Uwe Schulz, Karl-Otto Dubowy, Jens Tiesmeier, Kai-Thorsten Laser, Hendrik Bante, Leonard Bergau, Philipp Sommer, Henrik Fox, Michiel Morshuis, Jan Gummert, Hendrik Milting
Cardiomyopathy-associated mutations in the RS domain affect nuclear localization of RBM20. Human mutation 41 (11) (2020)
Anna Gaertner, Andreas Brodehl, Hendrik Milting
Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene? Protein & cell 10 (6) (2019)
Anna Gaertner, Jens Tiesmeier, Thomas Jakob, Bernd Strickmann, Gunter Veit, Bernd Bachmann-Mennenga, Lech Paluszkiewicz, Karin Klingel, Uwe Schulz, Kai T Laser, Bernd Karger, Heidi Pfeiffer, Hendrik Milting
Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy. Molecular genetics & genomic medicine 7 (8) (2019)