Stefan Kääb

发表

New algorithms and new technologies in computerized ECG analysis: a challenge in long-term follow-up studies

Karl-Hans Englmeier, Christine Meisinger, Siegfried Perz, 2013 .

Bioinformatics for Medical Diagnostics: Assessment of Microarray Data in the Context of Clinical Databases

Martin Dugas, Torsten Haferlach, Stefan Kääb, 2003, AMIA.

Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

Takeshi Tsuchiya, Thomas Meitinger, Tatsuhiko Tsunoda, 2014, Circulation. Cardiovascular genetics.

Identification of a common gene expression signature in dilated cardiomyopathy across independent microarray studies.

Ulrich Mansmann, Holger Sültmann, Markus Ruschhaupt, 2006, Journal of the American College of Cardiology.

Relation of increased short-term variability of QT interval to congenital long-QT syndrome.

Stefan Kääb, Martin Hinterseer, Gerhard Steinbeck, 2009, The American journal of cardiology.

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation.

Thomas Meitinger, Dan M Roden, Josée Dupuis, 2008, European heart journal.

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.

Benjamin Meder, Andreas Keller, Thomas Meitinger, 2014, European heart journal.

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Thomas Meitinger, Peter J. Schwartz, Walter J. Chazin, 2013, Circulation.

Nature Genetics Advance Online Publication Genetic Association Study of Qt Interval Highlights Role for Calcium Signaling Pathways in Myocardial Repolarization

Michael J Ackerman, Christian Gieger, Thomas Meitinger, 2022 .

Calcium-Handling Abnormalities Underlying Atrial Arrhythmogenesis and Contractile Dysfunction in Dogs With Congestive Heart Failure

Stanley Nattel, Yung-Hsin Yeh, Ursula Ravens, 2008, Circulation. Arrhythmia and electrophysiology.

Functional profiling of human atrial and ventricular gene expression

Stefan Kääb, Gerhard Steinbeck, Sylvia Merk, 2005, Pflügers Archiv.

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.

Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25

Eric Boerwinkle, Annette Peters, John Barnard, 2010, Circulation.

Genome-wide association analysis identifies multiple loci related to resting heart rate.

Christian Gieger, Thomas Meitinger, Henry Völzke, 2010, Human molecular genetics.

Clinical utility gene card for: Long-QT Syndrome (types 1–13)

Stefan Kääb, A. Wilde, S. Kääb, 2013, European Journal of Human Genetics.

Contrast enhanced transesophageal echocardiography in patients with atrial fibrillation referred to electrical cardioversion improves atrial thrombus detection and may reduce associated thromboembolic events

Johannes Rieber, Stefan Kääb, J. Rieber, 2013, Cardiovascular Ultrasound.

52 Genetic Loci Influencing Myocardial Mass.

Christian Gieger, Thomas Meitinger, Manolis Kellis, 2016, Journal of the American College of Cardiology.

Susceptibility genes and modifiers for cardiac arrhythmias.

Stefan Kääb, Eric Schulze-Bahr, E. Schulze-Bahr, 2005, Cardiovascular research.

Cellular basis of ventricular arrhythmias and abnormal automaticity in heart failure

Stefan Kääb, Eduardo Marbán, D. Kass, 1999 .

Keep it simple: the ECG and sudden cardiac death risk

Stefan Kääb, S. Kääb, Moritz F. Sinner, 2019, Heart.

Risk stratification for sudden cardiac death: current status and challenges for the future

Maarten L. Simoons, Marek Malik, Karl Swedberg, 2014, European heart journal.

Reprogramming of the Human Atrial Transcriptome in Permanent Atrial Fibrillation: Expression of a Ventricular-Like Genomic Signature

Stefan Kääb, Martin Hinterseer, Gerhard Steinbeck, 2005, Circulation research.

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

Christian Gieger, Thomas Meitinger, Raimund Erbel, 2009, Nature Genetics.

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.

Recent advances in the molecular pathophysiology of atrial fibrillation.

Niels Voigt, Stanley Nattel, Dobromir Dobrev, 2011, The Journal of clinical investigation.

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

Christian Gieger, Thomas Meitinger, Chao-Yu Guo, 2006, Nature Genetics.

Sotalol testing unmasks altered repolarization in patients with suspected acquired long-QT-syndrome--a case-control pilot study using i.v. sotalol.

Stefan Kääb, Martin Hinterseer, Gerhard Steinbeck, 2003, European heart journal.

Impact of real-time contact force and impedance measurement in pulmonary vein isolation procedures for treatment of atrial fibrillation

Sebastian Clauss, Reza Wakili, Stefan Kääb, 2014, Clinical Research in Cardiology.

Women and men with stable coronary artery disease have similar clinical outcomes: insights from the international prospective CLARIFY registry

Jean-Claude Tardif, Roberto Ferrari, Stefan Kääb, 2012, European heart journal.

Genome-wide association study of PR interval

Christian Gieger, Thomas Meitinger, Jan A. Kors, 2010, Nature Genetics.

Simple Risk Model Predicts Incidence of Atrial Fibrillation in a Racially and Geographically Diverse Population: the CHARGE‐AF Consortium

David D. McManus, Vilmundur Gudnason, Michael J. Pencina, 2013, Journal of the American Heart Association.

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

Jingyuan Fu, Thomas Meitinger, Jan A. Kors, 2010, Nature Genetics.

Global gene expression in human myocardium—oligonucleotide microarray analysis of regional diversity and transcriptional regulation in heart failure

Stefan Kääb, Gerhard Steinbeck, Sylvia Merk, 2004, Journal of Molecular Medicine.

Drug-Sensitized Zebrafish Screen Identifies Multiple Genes, Including GINS3, as Regulators of Myocardial Repolarization

Dan M Roden, Aravinda Chakravarti, Stefan Kääb, 2009, Circulation.

Lack of replication in polymorphisms reported to be associated with atrial fibrillation.

Thomas Meitinger, Annette Peters, Siegfried Perz, 2011, Heart rhythm.

Genetics of Atrial Fibrillation: Implications for Future Research Directions and Personalized Medicine

Stefan Kääb, E. Benjamin, P. Ellinor, 2010, Circulation. Arrhythmia and electrophysiology.

Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation

Thomas Meitinger, Andres Metspalu, Dan M. Roden, 2010, Nature Genetics.

Large-Scale Candidate Gene Analysis in Whites and African Americans Identifies IL6R Polymorphism in Relation to Atrial Fibrillation: The National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) Project

Sudha Seshadri, Thomas H Mosley, Martina Müller-Nurasyid, 2011, Circulation. Cardiovascular genetics.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Claude Bouchard, William Wheeler, Peter Kraft, 2014 .

Multiple Potential Molecular Contributors to Atrial Hypocontractility Caused by Atrial Tachycardia Remodeling in Dogs

Niels Voigt, Jean-Claude Tardif, Ulrich Schotten, 2010, Circulation. Arrhythmia and electrophysiology.