S. Zumhagen

发表

A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes

Marylyn D. Ritchie, Thomas Meitinger, Dana C. Crawford, 2012, Circulation. Cardiovascular genetics.

Totally Subcutaneous Implantable Cardioverter Defibrillator with an Alternative, Right Parasternal, Electrode Placement

L. Eckardt, E. Schulze-Bahr, A. Grace, 2012, Pacing and clinical electrophysiology : PACE.

POPDC2 a novel susceptibility gene for conduction disorders.

E. Arbustini, E. Schulze-Bahr, C. Rapezzi, 2020, Journal of molecular and cellular cardiology.

Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype

J. Rogers, E. Schulze-Bahr, A. Coffey, 2013, Basic Research in Cardiology.

A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction

E. Schulze-Bahr, G. Seebohm, S. Rinné, 2017, Circulation research.

Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking.

S. Hohnloser, E. Schulze-Bahr, S. Nattel, 2016, European heart journal.

Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: a long-term follow-up.

H. Scheld, P. Milberg, K. Wasmer, 2012, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

Intraoperative Defibrillation Testing of Subcutaneous Implantable Cardioverter‐Defibrillator Systems—A Simple Issue?

L. Eckardt, D. Dechering, S. Zumhagen, 2016, Journal of the American Heart Association.

Safety of endomyocardial biopsy in patients with arrhythmogenic right ventricular cardiomyopathy: a study analyzing 161 diagnostic procedures.

G. Breithardt, J. Stypmann, E. Schulze-Bahr, 2011, JACC. Cardiovascular interventions.

Long-term follow-up of subcutaneous ICD systems in patients with hypertrophic cardiomyopathy: a single-center experience

L. Eckardt, D. Dechering, S. Zumhagen, 2015, Clinical Research in Cardiology.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

R. Redon, E. Behr, D. Roden, 2013, Nature Genetics.

Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia.

M. Borggrefe, E. Schulze-Bahr, G. Seebohm, 2016, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography

E. Schulze-Bahr, K. Schäfers, L. Stegger, 2017, Heart.

Limitations in S-ICD therapy: reasons for system explantation

L. Eckardt, D. Dechering, S. Zumhagen, 2015, Clinical Research in Cardiology.

T peak – T end interval and T peak – T end /QT ratio in patients with Brugada syndrome

L. Eckardt, E. Schulze-Bahr, B. Stallmeyer, 2016 .

QT interval prolongation and risk for cardiac events in genotyped LQTS-index children

G. Breithardt, G. Mönnig, E. Schulze-Bahr, 2009, European Journal of Pediatrics.

Genes Causing Inherited Forms of Cardiomyopathies

E. Schulze-Bahr, M. Paul, T. Spieker, 2009, Herz Kardiovaskuläre Erkrankungen.

Corneal Densitometry as a Novel Technique for Monitoring Amiodarone Therapy.

G. Mönnig, N. Eter, L. Zumhagen, 2016, Ophthalmology.

Mutational spectrum in the Ca2+‐activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

Eric Schulze-Bahr, Sven Zumhagen, E. Schulze-Bahr, 2012, Human mutation.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Dan M Roden, Beverley Balkau, Pierre Lindenbaum, 2013, Nature Genetics.

Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes

R. Altman, Yufeng Shen, Yusuke Nakamura, 2013, PloS one.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

R. Redon, P. Lambiase, P. Ellinor, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

T. Werge, P. Ellinor, S. Priori, 2020, Circulation.

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

J. Towbin, J. Brugada, R. Brugada, 2010, Heart rhythm.

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

S. Tezenas du Montcel, W. Shimizu, E. Schulze-Bahr, 2015, European Journal of Human Genetics.

Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder

E. Schulze-Bahr, S. Rinné, N. Decher, 2014, EMBO molecular medicine.

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

T. Meitinger, D. Roden, A. Pfeufer, 2015, Circulation. Cardiovascular genetics.

Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome.

E. Schulze-Bahr, F. Sachse, A. Coffey, 2015, Journal of molecular and cellular cardiology.

Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGs

G. Mönnig, L. Eckardt, E. Schulze-Bahr, 2016, PloS one.

Overlapping Cardiac Phenotype Associated with a Familial Mutation in the Voltage Sensor of the KCNQ1 Channel

E. Schulze-Bahr, F. Lang, G. Seebohm, 2012, Cellular Physiology and Biochemistry.

Absence of Pathognomonic or Inflammatory Patterns in Cardiac Biopsies From Patients With Brugada Syndrome

G. Breithardt, L. Eckardt, E. Schulze-Bahr, 2008, Circulation: Arrhythmia and Electrophysiology.

High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literature.

E. Schulze-Bahr, C. Bode, B. Stiller, 2015, Journal of cardiology cases.

Sodium permeable and “hypersensitive” TREK‐1 channels cause ventricular tachycardia

E. Schulze-Bahr, P. Kohl, G. Seemann, 2017, EMBO molecular medicine.

A Heterozygous Deletion Mutation in the Cardiac Sodium Channel Gene SCN5A with Loss- and Gain-of-Function Characteristics Manifests as Isolated Conduction Disease, without Signs of Brugada or Long QT Syndrome

L. Eckardt, E. Schulze-Bahr, M. Paul, 2013, PloS one.

Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndrome.

L. Eckardt, E. Schulze-Bahr, B. Stallmeyer, 2016, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Inherited long QT syndrome

L. Eckardt, E. Schulze-Bahr, G. Seebohm, 2012, Herzschrittmachertherapie + Elektrophysiologie.

(Tpeak - Tend)/QRS and (Tpeak - Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply.

L. Eckardt, E. Schulze-Bahr, B. Stallmeyer, 2017, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Pairwise Feature Interactions to Predict Arrhythmic Risk of Brugada Syndrome

Konstantinos P. Letsas, Gary Tse, Qingpeng Zhang, 2021, 2021 Computing in Cardiology (CinC).

Brugada‐like cardiac disease in myotonic dystrophy type 2: report of two unrelated patients

K. Zerres, S. Rudnik-Schöneborn, W. Kress, 2011, European journal of neurology.

Overlapping Cardiac Phenotype Associated with a Familial Mutation in the Voltage Sensor of the KCNQ1 Channel

E. Schulze-Bahr, F. Lang, G. Seebohm, 2012, Cellular Physiology and Biochemistry.

Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome.

E. Schulze-Bahr, F. Sachse, A. Coffey, 2015, Journal of molecular and cellular cardiology.

Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K+ Channel) Channel Function

E. Schulze-Bahr, L. Pott, G. Seebohm, 2019, Circulation. Genomic and precision medicine.

Analysis for genetic modifiers of disease severity in patients with Long QT Syndrome

T. Meitinger, D. Roden, A. Pfeufer, 2016 .