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B. Gerull · SciRah

Researcher profile · Semantic Scholar

B. Gerull

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B. Gerull — researcher profile on SciRah

h-index: 36
Works: 115
Citations: 5,872

Most-cited papers

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing
Wei Guo, S. Schafer, Marion L. Greaser, M. Radke +24 more
2012Nature Medicine598 citations Open access
Semantic Scholar
Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction
S. Klaassen, Susanne Probst, E. Oechslin, B. Gerull +12 more
2008Circulation445 citations Open access
Semantic Scholar
Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care
S. Sawyer, T. Hartley, D. Dyment, C. Beaulieu +41 more
2015Clinical Genetics380 citations Open access
Semantic Scholar
Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy
A. Brodehl, R. Ferrier, S. Hamilton, S. Greenway +9 more
2016Human Mutation178 citations Open access
Semantic Scholar
Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy
M. Gramlich, L. S. Pane, Qifeng Zhou, Zhifen Chen +19 more
2015EMBO Molecular Medicine128 citations Open access
Semantic Scholar
Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease
M. Gramlich, Beate Michely, C. Krohne, A. Heuser +10 more
2009Journal of Molecular and Cellular Cardiology112 citations Open access
Semantic Scholar
Titin mutation in familial restrictive cardiomyopathy.
Y. Peled, M. Gramlich, G. Yoskovitz, M. Feinberg +12 more
2014International Journal of Cardiology99 citations
Semantic Scholar
Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry)
G. Mellor, Z. Laksman, R. Tadros, Jason D. Roberts +16 more
2017Circulation: Cardiovascular Genetics91 citations Open access
Semantic Scholar
Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy
B. Gerull, J. Atherton, Anke Geupel, Sabine Sasse-Klaassen +6 more
2006Journal of molecular medicine86 citations
Semantic Scholar
Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry
A. Herman, C. Cheung, B. Gerull, C. Simpson +18 more
2016Circulation: Arrhythmia and Electrophysiology74 citations
Semantic Scholar
Molecular Insights into Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Plakophilin-2 Missense Mutations
F. Kirchner, A. Schuetz, L. Boldt, Kristina Martens +5 more
2012Circulation: Cardiovascular Genetics69 citations
Semantic Scholar
The Genetic Landscape of Cardiomyopathies
B. Gerull, S. Klaassen, A. Brodehl
2019Genetic Causes of Cardiac Disease68 citations
Semantic Scholar
Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect
A. Brodehl, Seyed Ahmad Pour Hakimi, C. Stanasiuk, S. Ratnavadivel +6 more
2019Genes65 citations Open access
Semantic Scholar
Transgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling
A. Brodehl, D. Belke, L. Garnett, Kristina Martens +7 more
2017PLoS ONE65 citations Open access
Semantic Scholar
Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy
B. Gerull, A. Brodehl
2021Current Heart Failure Reports62 citations Open access
Semantic Scholar
Homozygous Founder Mutation in Desmocollin-2 (DSC2) Causes Arrhythmogenic Cardiomyopathy in the Hutterite Population
B. Gerull, F. Kirchner, Jessica X. Chong, Julia Tagoe +5 more
2013Circulation: Cardiovascular Genetics57 citations Open access
Semantic Scholar
Epinephrine Infusion in the Evaluation of Unexplained Cardiac Arrest and Familial Sudden Death: From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry
A. Krahn, J. Healey, V. Chauhan, D. Birnie +14 more
2012Circulation: Arrhythmia and Electrophysiology53 citations Open access
Semantic Scholar
The Rapidly Evolving Role of Titin in Cardiac Physiology and Cardiomyopathy.
B. Gerull
2015Canadian Journal of Cardiology50 citations
Semantic Scholar
Procainamide infusion in the evaluation of unexplained cardiac arrest: from the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER).
R. Somani, A. Krahn, J. Healey, V. Chauhan +16 more
2014Heart Rhythm50 citations
Semantic Scholar
Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry
C. Steinberg, G. Padfield, J. Champagne, S. Sanatani +15 more
2016Circulation: Arrhythmia and Electrophysiology47 citations Open access
Semantic Scholar
Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2
Nelly Abdelfatah, Ru-Ping Chen, H. Duff, C. Seifer +9 more
2019JACC: Basic to Translational Science46 citations Open access
Semantic Scholar
Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect.
A. Brodehl, M. Dieding, Niklas Biere, A. Unger +9 more
2016Journal of Molecular and Cellular Cardiology46 citations
Semantic Scholar
Genetic Animal Models for Arrhythmogenic Cardiomyopathy
B. Gerull, A. Brodehl
2020Frontiers in Physiology43 citations Open access
Semantic Scholar
Mutations in ILK, encoding integrin linked kinase, are associated with arrhythmogenic cardiomyopathy
A. Brodehl, S. Rezazadeh, T. Williams, N. Munsie +12 more
2019Translational Research: The Journal of Laboratory and Clinical Medicine41 citations Open access
Semantic Scholar
Mitofusin 2 Is Essential for IP3-Mediated SR/Mitochondria Metabolic Feedback in Ventricular Myocytes
L. Seidlmayer, Christine Mages, Annette Berbner, Petra Eder-Negrin +9 more
2019Frontiers in Physiology40 citations Open access
Semantic Scholar
A novel titin mutation in adult-onset familial dilated cardiomyopathy.
G. Yoskovitz, Y. Peled, M. Gramlich, H. Lahat +7 more
2012American Journal of Cardiology39 citations
Semantic Scholar
Genetic Insights into Primary Restrictive Cardiomyopathy
A. Brodehl, B. Gerull
2022Journal of Clinical Medicine38 citations Open access
Semantic Scholar
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect.
S. Greenway, R. McLeod, Stacey Hume, N. Roslin +8 more
2014Canadian Journal of Cardiology37 citations
Semantic Scholar
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3
Jirko Kühnisch, C. Herbst, N. Al-Wakeel-Marquard, J. Dartsch +13 more
2019Clinical Genetics36 citations Open access
Semantic Scholar
A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy.
A. Brodehl, J. Weiss, Jana Davina Debus, C. Stanasiuk +13 more
2020Journal of Molecular and Cellular Cardiology35 citations Open access
Semantic Scholar
Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype
K. Kolokotronis, Jirko Kühnisch, E. Klopocki, J. Dartsch +7 more
2019Human Mutation35 citations
Semantic Scholar
Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?
Jason D. Roberts, A. Krahn, M. Ackerman, Ram K. Rohatgi +28 more
2017Circulation: Arrhythmia and Electrophysiology35 citations Open access
Semantic Scholar
Evolution of clinical diagnosis in patients presenting with unexplained cardiac arrest or syncope due to polymorphic ventricular tachycardia.
Maria Vittoria Matassini, A. Krahn, M. Gardner, J. Champagne +11 more
2014Heart Rhythm31 citations
Semantic Scholar
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset
A. Brodehl, A. Meshkov, R. Myasnikov, A. Kiseleva +21 more
2021International Journal of Molecular Sciences27 citations Open access
Semantic Scholar
The Pore-Lipid Interface: Role of Amino-Acid Determinants of Lipophilic Access by Ivabradine to the hERG1 Pore Domain
Laura L. Perissinotti, Ji-Qing Guo, Meruyert Kudaibergenova, J. Lees-Miller +7 more
2019Molecular Pharmacology26 citations Open access
Semantic Scholar
Cardiomyocyte adhesion and hyperadhesion differentially require ERK1/2 and plakoglobin
Maria Shoykhet, Sebastian Trenz, Ellen Kempf, T. Williams +4 more
2020JCI Insight23 citations Open access
Semantic Scholar
Genetic Association Study in Multigenerational Kindreds With Vasovagal Syncope: Evidence for Involvement of Sex-Specific Serotonin Signaling
R. Sheldon, M. Rose, D. Ritchie, Kristina Martens +4 more
2019Circulation: Arrhythmia and Electrophysiology21 citations Open access
Semantic Scholar
Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy
Ru-Ping Chen, Simone Buchmann, Amos Kroth, Anahi-Paula Arias-Loza +10 more
2023Circulation Research20 citations Open access
Semantic Scholar
Plakophilin 2 regulates intestinal barrier function by modulating protein kinase C activity in vitro
Simon Nagler, Yalda Ghoreishi, Cathérine Kollmann, M. Kelm +4 more
2022Tissue Barriers17 citations Open access
Semantic Scholar
Meeting report - Desmosome dysfunction and disease: Alpine desmosome disease meeting.
V. Spindler, B. Gerull, K. Green, A. Kowalczyk +12 more
2023Journal of Cell Science16 citations Open access
Semantic Scholar
A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients
Emilia Nagyova, E. Hoorntje, W. T. te Rijdt, L. Bosman +37 more
2023Journal of Cardiovascular Translational Research16 citations Open access
Semantic Scholar
Investigating LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Y. Shemer, L. Mekies, R. Ben Jehuda, P. Baskin +9 more
2021International Journal of Molecular Sciences16 citations Open access
Semantic Scholar
Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish
M. Zink, Anne Seewald, Mareike Rohrbach, A. Brodehl +4 more
2022International Journal of Molecular Sciences14 citations Open access
Semantic Scholar
Immuno-metabolic interfaces in cardiac disease and failure.
E. Bertero, Jan Dudek, C. Cochain, M. Delgobo +8 more
2021Cardiovascular Research14 citations
Semantic Scholar
Novel c.367_369del LMNA mutation manifesting as severe arrhythmias, dilated cardiomyopathy, and myopathy.
H. Keller, J. Finsterer, C. Steger, P. Wexberg +6 more
2012Heart & lung : the journal of critical care14 citations
Semantic Scholar
EGFR inhibition leads to enhanced desmosome assembly and cardiomyocyte cohesion via ROCK activation
Maria Shoykhet, O. Dervishi, Philipp Menauer, Matthias Hiermaier +10 more
2023JCI Insight13 citations Open access
Semantic Scholar
Spatial relationship between mitral valve and ventricular septum assessed by resting echocardiography to diagnose left ventricular outflow tract obstruction in hypertrophic cardiomyopathy
N. Verheyen, A. Batzner, D. Zach, A. Zirlik +6 more
2023European Heart Journal-Cardiovascular Imaging11 citations Open access
Semantic Scholar
Phenotypic Analysis of Arrhythmogenic Cardiomyopathy in the Hutterite Population: Role of Electrocardiogram in Identifying High‐Risk Desmocollin‐2 Carriers
J. Wong, H. Duff, T. Yuen, Louis Kolman +3 more
2014Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease10 citations Open access
Semantic Scholar
Non-invasive estimation of left ventricular systolic peak pressure: a prerequisite to calculate myocardial work in hypertrophic obstructive cardiomyopathy
A. Batzner, P. Hahn, C. Morbach, S. Störk +5 more
2023European Heart Journal-Cardiovascular Imaging9 citations Open access
Semantic Scholar
Ultra-high field cardiac MRI in large animals and humans for translational cardiovascular research
L. Schreiber, D. Lohr, Steffen Baltes, U. Vogel +19 more
2023Frontiers in Cardiovascular Medicine9 citations Open access
Semantic Scholar

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