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Recent advances in the molecular pathophysiology of atrial fibrillation

The Journal of clinical investigation, 2011-08, Vol.121 (8), p.2955-2968

2011

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Animal Models of Atrial Fibrillation

Circulation research, 2020-06, Vol.127 (1), p.91-110

2020

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Genomic risk scores, biomolecules, and clinical conditions to predict atrial fibrillation: time to integrate what we can measure

European heart journal, 2023-01, Vol.44 (3), p.232-234

2023

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Procoagulant platelet sentinels prevent inflammatory bleeding through GPIIBIIIA and GPVI

Blood, 2022-07, Vol.140 (2), p.121-139

2022

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Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Circulation (New York, N.Y.), 2013-03, Vol.127 (9), p.1009-1017

2013

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Chronically elevated branched chain amino acid levels are pro-arrhythmic

Cardiovascular research, 2022-06, Vol.118 (7), p.1742-1757

2022

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Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol

Journal of the American College of Cardiology, 2012-11, Vol.60 (20), p.2092-2099

2012

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Evidence for increased SARS-CoV-2 susceptibility and COVID-19 severity related to pre-existing immunity to seasonal coronaviruses

Cell reports (Cambridge), 2021-12, Vol.37 (13), p.110169-110169, Article 110169

2021

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Non-coding RNA and Cardiac Electrophysiological Disorders

Non-coding RNAs in Cardiovascular Diseases, p.301-310

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Ventricular Fibrillation with Prominent Early Repolarization Associated with a Rare Variant of KCNJ8/KATP Channel

Journal of cardiovascular electrophysiology, 2009-01, Vol.20 (1), p.93-98

2009

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Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

The Journal of clinical investigation, 2008-06, Vol.118 (6), p.2260-2268

2008

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Clinical utility gene card for: Long-QT syndrome

European journal of human genetics : EJHG, 2021-12, Vol.29 (12), p.1825-1832

2021

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Central retinal artery occlusion as a first sign of atrial fibrillation: A 3‐year retrospective single‐center analysis

Clinical cardiology (Mahwah, N.J.), 2021-12, Vol.44 (12), p.1654-1661

2021

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Early repolarization pattern is the strongest predictor of arrhythmia recurrence in patients with idiopathic ventricular fibrillation: results from a single centre long-term follow-up over 20 years

Europace (London, England), 2016-05, Vol.18 (5), p.718-725

2016

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New challenges in cardiac intensive care units

Clinical research in cardiology, 2021-09, Vol.110 (9), p.1369-1379

2021

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Animal models of arrhythmia: classic electrophysiology to genetically modified large animals

Nature reviews cardiology, 2019-08, Vol.16 (8), p.457-475

2019

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Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients

BMC medical genetics, 2017-10, Vol.18 (1), p.113-113, Article 113

2017

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Early decision-analytic modeling - a case study on vascular closure devices

BMC health services research, 2015-10, Vol.15 (1), p.486-486, Article 486

2015

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Molekulargenetische Diagnostik bei hereditären Arrhythmiesyndromen heute und in Zukunft

Herzschrittmachertherapie & Elektrophysiologie, 2012-09, Vol.23 (3), p.161-166

2012

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Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics

European heart journal, 2022-05, Vol.43 (20), p.1901-1916

2022

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Precise Correction of Heterozygous SHOX2 Mutations in hiPSCs Derived from Patients with Atrial Fibrillation via Genome Editing and Sib Selection

Stem cell reports, 2020-10, Vol.15 (4), p.999-1013

2020

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Repolarization Heterogeneity Measured With T-Wave Area Dispersion in Standard 12-Lead ECG Predicts Sudden Cardiac Death in General Population

Circulation. Arrhythmia and electrophysiology, 2018-02, Vol.11 (2), p.e005762-e005762

2018

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Long QT Syndrome–Associated Mutations in KCNQ1 and KCNE1 Subunits Disrupt Normal Endosomal Recycling of IKs Channels

Circulation research, 2008-12, Vol.103 (12), p.1451-1457

2008

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How exercise can deteriorate the clinical course of an ARVC patient: a case report

European heart journal : case reports, 2021-11, Vol.5 (11), p.ytab417

2021

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Recent advances in the molecular pathophysiology of atrial fibrillation

Animal Models of Atrial Fibrillation

Genomic risk scores, biomolecules, and clinical conditions to predict atrial fibrillation: time to integrate what we can measure

Procoagulant platelet sentinels prevent inflammatory bleeding through GPIIBIIIA and GPVI

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Chronically elevated branched chain amino acid levels are pro-arrhythmic

Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol

Evidence for increased SARS-CoV-2 susceptibility and COVID-19 severity related to pre-existing immunity to seasonal coronaviruses

Non-coding RNA and Cardiac Electrophysiological Disorders

Ventricular Fibrillation with Prominent Early Repolarization Associated with a Rare Variant of KCNJ8/KATP Channel

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

Clinical utility gene card for: Long-QT syndrome

Central retinal artery occlusion as a first sign of atrial fibrillation: A 3‐year retrospective single‐center analysis

Atrial fibrillation in the presence and absence of heart failure enhances expression of genes involved in cardiomyocyte structure, conduction properties, fibrosis, inflammation, and endothelial dysfunction

Early repolarization pattern is the strongest predictor of arrhythmia recurrence in patients with idiopathic ventricular fibrillation: results from a single centre long-term follow-up over 20 years

New challenges in cardiac intensive care units

Animal models of arrhythmia: classic electrophysiology to genetically modified large animals

Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients

Early decision-analytic modeling - a case study on vascular closure devices

Molekulargenetische Diagnostik bei hereditären Arrhythmiesyndromen heute und in Zukunft

Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics

Precise Correction of Heterozygous SHOX2 Mutations in hiPSCs Derived from Patients with Atrial Fibrillation via Genome Editing and Sib Selection

Repolarization Heterogeneity Measured With T-Wave Area Dispersion in Standard 12-Lead ECG Predicts Sudden Cardiac Death in General Population

Long QT Syndrome–Associated Mutations in KCNQ1 and KCNE1 Subunits Disrupt Normal Endosomal Recycling of IKs Channels

How exercise can deteriorate the clinical course of an ARVC patient: a case report

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