Brenda Gerull

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 20

Top Topics

Left Ventricular

Top Venues

Circulation research

International journal of molecular sciences

European heart journal

Journal of clinical medicine

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

Publications

Julian Kammerer, Alexandra Cirnu, Tatjana Williams, Melanie Hasselmeier, Mike Nörpel, Ruping Chen, Brenda Gerull
Macro-based collagen quantification and segmentation in picrosirius red-stained heart sections using light microscopy. Biology methods & protocols 9 (1) (2024)
Julian Kammerer, Alexandra Cirnu, Tatjana Williams, Melanie Hasselmeier, Mike Nörpel, Ruping Chen, Brenda Gerull
Macro-based collagen quantification and segmentation in picrosirius red-stained heart sections using light microscopy. Biology methods & protocols 9 (1) (2024)
Ruping Chen, Simone Buchmann, Amos Kroth, Anahi Paula Arias-Loza, Michael Kohlhaas, Nicole Wagner, Gianna Grüner, Alexander G Nickel, Alexandra Cirnu, Tatjana Williams, Christoph Maack, Süleyman Ergün, Stefan Frantz, Brenda Gerull
Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy. Circulation research 132 (2) (2023)
Ruping Chen, Simone Buchmann, Amos Kroth, Anahi Paula Arias-Loza, Michael Kohlhaas, Nicole Wagner, Gianna Grüner, Alexander G Nickel, Alexandra Cirnu, Tatjana Williams, Christoph Maack, Süleyman Ergün, Stefan Frantz, Brenda Gerull
Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy. Circulation research 132 (2) (2023)
Ruping Chen, Simone Buchmann, Amos Kroth, Anahi Paula Arias-Loza, Michael Kohlhaas, Nicole Wagner, Gianna Grüner, Alexander G Nickel, Alexandra Cirnu, Tatjana Williams, Christoph Maack, Süleyman Ergün, Stefan Frantz, Brenda Gerull
Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy. Circulation research 132 (2) (2023)
Robert S Sheldon, Brenda Gerull
Have we found the genetic signature for vasovagal syncope? European heart journal (2023)
Angelika Batzner, Patrick Hahn, Caroline Morbach, Stefan Stoerk, Christoph Maack, Nicolas D Verheyen, Brenda Gerull, Stefan Frantz, Hubert Seggewiss
Non-invasive estimation of left ventricular systolic peak-pressure - a prerequisite to calculate myocardial work in hypertrophic obstructive cardiomyopathy. European heart journal. Cardiovascular Imaging (2023)
Ruping Chen, Simone Buchmann, Amos Kroth, Anahi Paula Arias-Loza, Michael Kohlhaas, Nicole Wagner, Gianna Grüner, Alexander G Nickel, Alexandra Cirnu, Tatjana Williams, Christoph Maack, Süleyman Ergün, Stefan Frantz, Brenda Gerull
Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy. Circulation research 132 (2) (2023)
Nicolas D Verheyen, Angelika Batzner, David Zach, Andreas Zirlik, Brenda Gerull, Stefan Frantz, Christoph Maack, Stefan Stoerk, Hubert Seggewiss, Caroline Morbach
Spatial relationship between mitral valve and ventricular septum assessed by resting echocardiography to diagnose left ventricular outflow tract obstruction in hypertrophic cardiomyopathy. European heart journal. Cardiovascular Imaging (2023)
Robert S Sheldon, Brenda Gerull
Have we found the genetic signature for vasovagal syncope? European heart journal 44 (12) (2023)
Andreas Brodehl, Brenda Gerull
Genetic Insights into Primary Restrictive Cardiomyopathy. Journal of clinical medicine 11 (8) (2022)
Simon Nagler, Yalda Ghoreishi, Catherine Kollmann, Matthias Kelm, Brenda Gerull, Jens Waschke, Natalie Burkard, Nicolas Schlegel
Plakophilin 2 regulates intestinal barrier function by modulating protein kinase C activity in vitro. Tissue barriers (2022)
Miriam Zink, Anne Seewald, Mareike Rohrbach, Andreas Brodehl, Daniel Liedtke, Tatjana Williams, Sarah J Childs, Brenda Gerull
Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish. International journal of molecular sciences 23 (17) (2022)
Brenda Gerull, Andreas Brodehl
Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy. Current heart failure reports 18 (6) (2021)
Yuval Shemer, Lucy N Mekies, Ronen Ben Jehuda, Polina Baskin, Rita Shulman, Binyamin Eisen, Danielle Regev, Arbustini Eloisa, Brenda Gerull, Mihaela Gherghiceanu, Eyal Gottlieb, Michael Arad, Ofer Binah
Investigating LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. International journal of molecular sciences 22 (15) (2021)
Andreas Brodehl, Hendrik Milting, Brenda Gerull
Special Issue "Cardiovascular Genetics". Genes 12 (4) (2021)
Andreas Brodehl, Alexey Nikolaevich Meshkov, Roman P Myasnikov, Anna Vitalievna Kiseleva, Olga V Kulikova, Bärbel Klauke, Evgeniia Sotnikova, Caroline Stanasiuk, Mikhail G Divashuk, Greta Marie Pohl, Maria Kudryavtseva, Karin Klingel, Brenda Gerull, Anastasia Zharikova, Jan Gummert, Sergey N Koretskiy, Stephan Schubert, Elena A Mershina, Anna Gärtner, Polina Pilus, Kai Thorsten Laser, Valentin E Sinitsyn, Sergey Boytsov, Oksana M Drapkina, Hendrik Milting
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset. International journal of molecular sciences 22 (7) (2021)
Konstantinos Kolokotronis, Natalie Pluta, Eva Klopocki, Erdmute Kunstmann, Daniel R Messroghli, Christoph Maack, Shai Tejman-Yarden, Michael Arad, Simone Rost, Brenda Gerull
New Insights on Genetic Diagnostics in Cardiomyopathy and Arrhythmia Patients Gained by Stepwise Exome Data Analysis. Journal of clinical medicine 9 (7) (2020)
Andreas Brodehl, Seyed Ahmad Pour Hakimi, Caroline Stanasiuk, Sandra Ratnavadivel, Doris Hendig, Anna Gaertner, Brenda Gerull, Jan Gummert, Lech Paluszkiewicz, Hendrik Milting
Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect. Genes 10 (11) (2019)
Konstantinos Kolokotronis, Jirko Kühnisch, Eva Klopocki, Josephine Dartsch, Simone Rost, Cathleen Huculak, Giulia Mearini, Stefan Störk, Lucie Carrier, Sabine Klaassen, Brenda Gerull
Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype. Human mutation 40 (8) (2019)