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Barbara J.M. Mulder

St. Antonius Ziekenhuis · NL
Area of research
Epidemiology · Pulmonary and Respiratory Medicine
Research interest
Research interests include Congenital Heart Disease Studies, Cardiac Valve Diseases and Treatments, Aortic Disease and Treatment Approaches, and Pulmonary Hypertension Research and Treatments.
h-index
90
citations
38,894
works
725
NIH funding
primary concept
email

Recent publications

Value of Extended Arrhythmia Screening in Adult Congenital Heart Disease Patients
Arrhythmia & Electrophysiology Review 2024cited by 3position: contributordoi
Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials
The Lancet 2022cited by 109position: middledoi
Identification of patients at risk of sudden cardiac death in congenital heart disease: The PRospEctiVE study on implaNTable cardIOverter defibrillator therapy and suddeN cardiac death in Adults with Congenital Heart Disease (PREVENTION-ACHD)
Heart Rhythm 2021cited by 49position: middledoi
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries
Circulation Research 2021cited by 38position: middledoi
Final comment on the debate article “ICD implantation as primary prevention in systemic RV”
International Journal of Cardiology Congenital Heart Disease 2021cited by 0position: contributordoi
ICD implantation as primary prevention in systemic RV? A cautious attitude is justified
International Journal of Cardiology Congenital Heart Disease 2021cited by 0position: contributordoi
Bleeding and thrombotic risk in pregnant women with Fontan physiology
Heart 2020cited by 24position: middledoi
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
Circulation Research 2019cited by 197position: middledoi
Non-vitamin K antagonist oral anticoagulants (NOACs) for thromboembolic prevention, are they safe in congenital heart disease? Results of a worldwide study
International Journal of Cardiology 2019cited by 81position: lastdoi
Glycoproteomic Analysis of the Aortic Extracellular Matrix in Marfan Patients
Arteriosclerosis Thrombosis and Vascular Biology 2019cited by 54position: middledoi
Education as important predictor for successful employment in adults with congenital heart disease worldwide
Congenital Heart Disease 2019cited by 45position: lastdoi
European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants
Orphanet Journal of Rare Diseases 2019cited by 39position: middledoi
Maternal right ventricular function, uteroplacental circulation in first trimester and pregnancy outcome in women with congenital heart disease
Ultrasound in Obstetrics and Gynecology 2018cited by 29position: middledoi
European Society of Cardiology: Cardiovascular Disease Statistics 2017
European Heart Journal 2017cited by 945position: middledoi
Past and current cause-specific mortality in Eisenmenger syndrome
European Heart Journal 2017cited by 92position: middledoi
Value of Cardiovascular Magnetic Resonance Imaging in Noninvasive Risk Stratification in Tetralogy of Fallot
JAMA Cardiology 2017cited by 69position: middledoi
Effect of Losartan on Right Ventricular Dysfunction
Circulation 2017cited by 52position: middledoi
The natural history and surgical outcome of patients with scimitar syndrome: a multi-centre European study
European Heart Journal 2017cited by 41position: middledoi
QRS fragmentation is superior to QRS duration in predicting mortality in adults with tetralogy of Fallot
Heart 2016cited by 91position: middledoi
Sudden cardiac death in adult congenital heart disease: can the unpredictable be foreseen?
EP Europace 2016cited by 38position: middledoi
Uteroplacental Doppler flow and pregnancy outcome in women with tetralogy of Fallot
Ultrasound in Obstetrics and Gynecology 2016cited by 31position: middledoi
The care of adults with congenital heart disease across the globe: Current assessment and future perspective
International Journal of Cardiology 2015cited by 107position: middledoi
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect
Genetics in Medicine 2015cited by 50position: middledoi
Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' Collaboration
American Heart Journal 2015cited by 47position: middledoi
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
The American Journal of Human Genetics 2014cited by 186position: middledoi
Contemporary predictors of death and sustained ventricular tachycardia in patients with repaired tetralogy of Fallot enrolled in the INDICATOR cohort
Heart 2013cited by 497position: middledoi
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Nature Genetics 2013cited by 165position: middledoi
Uteroplacental Blood Flow, Cardiac Function, and Pregnancy Outcome in Women With Congenital Heart Disease
Circulation 2013cited by 111position: middledoi
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot
Human Molecular Genetics 2013cited by 109position: middledoi
Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease
Circulation Cardiovascular Genetics 2013cited by 53position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Maarten Groenink · GGz centraal6 papers (2013–2021)Berto J. Bouma · Amsterdam University of Applied Sciences6 papers (2012–2021)Aeilko H. Zwinderman · Public Health Service of Amsterdam6 papers (2016–2021)Arie P.J. van Dijk · Utrecht University5 papers (2013–2018)Martijn A. Oudijk · Netherlands Institute for Neuroscience3 papers (2013–2018)S. Matthijs Boekholdt · Amsterdam UMC Location University of Amsterdam3 papers (2012–2021) · 3 papers (2016–2017)Folkert J. Meijboom · University Medical Center Utrecht3 papers (2016–2017) · 3 papers (2021–2024)Jolien W. Roos‐Hesselink · Genetic Alliance3 papers (2013–2019)Petronella G. Pieper · Utrecht University3 papers (2013–2018)Henk Groen · Utrecht University3 papers (2013–2018)Werner Budts · Medical University of Lodz3 papers (2016–2021)Erwin Oechslin · Hospital for Sick Children3 papers (2015–2021) · 3 papers (2013–2021) · 3 papers (2016–2017)Dirk J. van Veldhuisen · AZ Sint-Jan3 papers (2013–2018) · 3 papers (2016–2017)M. A. M. Kampman · Utrecht University3 papers (2013–2018)Joris R. de Groot · Thrombolysis in Myocardial Infarction Study Group2 papers (2016–2021)