J. De Backer

发表

Aortic reflection coefficients and their association with global indexes of wave reflection in healthy controls and patients with Marfan's syndrome.

P Segers, J. De Sutter, P. Verdonck, 2006, American journal of physiology. Heart and circulatory physiology.

Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association.

K. Eagle, L. Hiratzka, S. Prakash, 2018, Circulation. Genomic and precision medicine.

Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the FBN1 Gene for Marfan Syndrome: Proposal for a Disease- and Gene-Specific Guideline

A. De Paepe, W. Steyaert, B. Callewaert, 2018, Circulation. Genomic and precision medicine.

Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan’s syndrome

G. Pals, E. E. van der Wall, B. Mulder, 2006, Heart.

Functional analysis of the common carotid artery: relative distension differences over the vessel wall measured in vivo

Pascal Verdonck, Patrick Segers, Stein Inge Rabben, 2004, Journal of hypertension.

Pregnancy outcomes in women with cardiovascular disease: evolving trends over 10 years in the ESC Registry Of Pregnancy And Cardiac disease (ROPAC).

K. Sliwa, R. Hall, L. Tavazzi, 2019, European heart journal.

Organisation of care for pregnancy in patients with congenital heart disease

J. Roos‐Hesselink, P. Kranke, L. Swan, 2017, Heart.

Heart failure in pregnant women with cardiac disease: data from the ROPAC

R. Hall, J. Roos‐Hesselink, P. Pieper, 2013, Heart.

Circulating Transforming Growth Factor-&bgr; in Marfan Syndrome

H. Dietz, J. Habashi, N. McDonnell, 2009, Circulation.

Diastolic dysfunction, infarct size, and exercise capacity in remote myocardial infarction: a combined approach of mitral E-wave deceleration time and color M-mode flow propagation velocity.

J. De Sutter, P. Verdonck, M. D. De Buyzere, 2002, The American journal of cardiology.

Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia.

A. De Paepe, S. Leikin, G. Gillessen‐kaesbach, 2015, American journal of human genetics.

Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic FBN1 Mutations

P. Robinson, E. Arbustini, U. Francke, 2009, Pediatrics.

Worsening in oxygen saturation and exercise capacity predict adverse outcome in patients with Eisenmenger syndrome.

J. Voigt, M. de Pauw, W. Budts, 2013, International journal of cardiology.

Creating the BELgian COngenital heart disease database combining administrative and clinical data (BELCODAC): Rationale, design and methodology.

A. Marelli, W. Budts, L. Annemans, 2020, International journal of cardiology.

Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome

G. Pals, S. Bierma-Zeinstra, J. Timmermans, 2011, Journal of Medical Genetics.

Outflow Through Aortic Side Branches Drives False Lumen Patency in Type B Aortic Dissection

I. van Herzeele, F. Vermassen, P. Segers, 2021, Frontiers in Cardiovascular Medicine.

Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients

A. De Paepe, B. Callewaert, P. Coucke, 2015, Orphanet Journal of Rare Diseases.

Influenza vaccination in congenital heart disease in the pre-COVID19 era: Coverage rate, patient characteristics and outcome.

W. Budts, L. Annemans, P. Moons, 2021, The Canadian journal of cardiology.

Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome

S. Blankenberg, C. Detter, K. Kutsche, 2019, Journal of clinical medicine.

Treatment of pre-existing cardiomyopathy during pregnancy

M. de Pauw, K. Roelens, J. De Backer, 2014 .

A new dimension in patent foramen ovale size estimation

D. De Wolf, D. Hemelsoet, B. Paelinck, 2020, Echocardiography.

Development of a transition program for adolescents with congenital heart disease

D. De Wolf, E. Goossens, L. Demulier, 2019, European Journal of Pediatrics.

New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections.

A. De Paepe, B. Callewaert, P. Coucke, 2013, Polskie Archiwum Medycyny Wewnetrznej.

Genes in Thoracic Aortic Aneurysms and Dissections – Do they Matter?

A. De Paepe, B. Callewaert, P. Coucke, 2013, AORTA.

Connective Tissue Disorders

S. Morris, J. De Backer, 2021, Echocardiography in Pediatric and Congenital Heart Disease.

European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

E. Arbustini, J. Timmermans, B. Mulder, 2019, Orphanet Journal of Rare Diseases.

Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variants.

J. Timmermans, F. Mattace-Raso, J. Roos‐Hesselink, 2012, Journal of the American College of Cardiology.

Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature

O. Gabrielli, C. Wallgren‐Pettersson, A. De Paepe, 2009, Human mutation.

Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.

J. De Sutter, T. de Ravel, Kristof Vandekerckhove, 2010, International journal of cardiology.

Arterial hypertension in Turner syndrome: a review of the literature and a practical approach for diagnosis and treatment.

D. De Wolf, T. D. de Backer, L. Demulier, 2015, Journal of hypertension.

Reference values for echocardiographic assessment of the diameter of the aortic root and ascending aorta spanning all age categories.

R. Devereux, D. De Wolf, M. Roman, 2014, The American journal of cardiology.

Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics

A. Evangelista, G. Jondeau, P. Gallego, 2019, European journal of preventive cardiology.

Real-world healthcare utilization in adult congenital heart disease: a systematic review of trends and ratios

L. Annemans, A. Werbrouck, J. De Backer, 2019, Cardiology in the Young.

Staffing, activities, and infrastructure in 96 specialised adult congenital heart disease clinics in Europe.

M. Schwerzmann, J. Roos‐Hesselink, G. Diller, 2019, International journal of cardiology.

Transfer and transition practices in 96 European adult congenital heart disease centres.

M. Schwerzmann, J. Roos‐Hesselink, G. Diller, 2020, International journal of cardiology.

SMAD3 pathogenic variants: risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium

S. Leal, D. Milewicz, D. Guo, 2019, Journal of Medical Genetics.

Marfan and Sartans: time to wake up!

J. De Backer, 2015, European heart journal.

Congenital heart disease Cardiovascular manifestations in men and women carrying a FBN 1 mutation

P. Robinson, E. Arbustini, U. Francke, 2010 .

The expanding cardiovascular phenotype of Marfan syndrome.

J. De Backer, 2009, European journal of echocardiography : the journal of the Working Group on Echocardiography of the European Society of Cardiology.

Connective Tissue Disorders

S. Morris, J. De Backer, 2021, Echocardiography in Pediatric and Congenital Heart Disease.

Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2.

A. De Paepe, S. Sharif, B. Callewaert, 2013, International journal of cardiology.

Sex, pregnancy and aortic disease in Marfan syndrome

D. Keene, L. Sakai, J. De Backer, 2017, PloS one.

International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium).

S. Lemaire, R. Jeremy, D. Milewicz, 2016, Circulation. Cardiovascular genetics.

Disproportion and dysmorphism in an adult Belgian population with Turner syndrome: risk factors for chronic diseases?

G. T’Sjoen, B. Callewaert, M. Craen, 2020, Acta clinica Belgica.

Cardiovascular imaging in Turner syndrome: state-of-the-art practice across the lifespan

J. Roos‐Hesselink, L. Lopez, C. Gravholt, 2018, Heart.

Cardiomyopathy in Genetic Aortic Diseases

J. De Backer, L. Muiño-Mosquera, 2021, Frontiers in Pediatrics.

Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome

Máté I. Tóth, R. Raedt, P. Sips, 2020, International journal of molecular sciences.

Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trial

A. De Paepe, D. Devos, J. De Backer, 2017, Acta cardiologica.

Type B aortic dissection triggered by heart transplantation in a patient with Marfan syndrome

M. de Pauw, J. De Backer, K. François, 2015, BMJ Case Reports.

Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy.

S. B. Wechsler, H. Dietz, L. Guey, 2013, American heart journal.

Echocardiographic methods, quality review, and measurement accuracy in a randomized multicenter clinical trial of Marfan syndrome.

S. Colan, L. Sleeper, L. Guey, 2013, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands

E. Arbustini, U. Francke, D. Halliday, 2008, Journal of Medical Genetics.

Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection.

A. F. Scott, D. Milewicz, H. Dietz, 2018, Journal of the American College of Cardiology.

Propagation-based phase-contrast synchrotron imaging of aortic dissection in mice: from individual elastic lamella to 3D analysis

M. Stampanoni, N. Stergiopulos, P. Segers, 2018, Scientific Reports.

Marfan syndrome.

D. Milewicz, A. Evangelista, G. Jondeau, 2021, Nature reviews. Disease primers.

Absence of Cardiovascular Manifestations in a Haploinsufficient Tgfbr1 Mouse Model

H. Dietz, P. Segers, A. De Paepe, 2014, PloS one.

Multiple aneurysms in a patient with aneurysms-osteoarthritis syndrome.

I. van Herzeele, F. Vermassen, A. De Paepe, 2013, The Annals of thoracic surgery.

T. Travison, S. Colan, J. Krischer, 2019, The Journal of pediatrics.

First report of the genetic background of Marfan syndrome in Polish patients.

A. De Paepe, P. Coucke, J. De Backer, 2013, Polskie Archiwum Medycyny Wewnetrznej.

Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome

G. Pals, A. De Paepe, B. Loeys, 2004, Human mutation.

Genetic testing for aortopathies: primer for the nongeneticist.

G. Jondeau, C. Boileau, J. De Backer, 2019, Current opinion in cardiology.

Pregnancy in Women With SMAD3 Mutation.

J. Roos‐Hesselink, D. van der Linde, I. M. van de Laar, 2017, Journal of the American College of Cardiology.

Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study.

A. Evangelista, A. Pini, G. Jondeau, 2022, European journal of medical genetics.

QT dispersion is not related to infarct size or inducibility in patients with coronary artery disease and life threatening ventricular arrhythmias

L. Jordaens, J. De Sutter, G. De Backer, 1999, Heart.

Hereditary thoracic aortic disease: How to save lives.

M. Roman, J. De Backer, 2021, The Journal of thoracic and cardiovascular surgery.

Effects of fibrillin mutations on the behavior of heart muscle cells in Marfan syndrome

Louis Van der Meeren, A. Skirtach, S. Sinha, 2020, Scientific Reports.

Vascular Ehlers-Danlos Syndrome Management: The Paris Way, A Step Forward on a Long Road.

T. D. de Backer, J. De Backer, Tine De Backer, 2019, Journal of the American College of Cardiology.

The spectrum of spontaneous coronary artery dissection: illustrated review of the literature

T. D. de Backer, D. Devos, J. De Backer, 2017, Acta cardiologica.

Three arginine to cysteine substitutions in the pro‐alpha (I)‐collagen chain cause Ehlers‐Danlos syndrome with a propensity to arterial rupture in early adulthood

A. De Paepe, N. Sakalihasan, P. Coucke, 2007, Human mutation.

Association of Mitral Annular Disjunction With Cardiovascular Outcomes Among Patients With Marfan Syndrome.

F. Timmermans, M. Duytschaever, J. De Backer, 2021, JAMA cardiology.

The 'Ten Commandments' in Adult Congenital Heart Disease Guidelines.

H. Baumgartner, J. De Backer, 2020, European heart journal.

The Belgian Eisenmenger syndrome registry: Implications for treatment strategies?

M. de Pauw, W. Budts, R. Naeije, 2009, Acta cardiologica.

Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy.

W. van Biesen, R. Vanholder, A. De Paepe, 2013, International journal of cardiology.

The 2017 international classification of the Ehlers–Danlos syndromes

J. Belmont, P. Byers, R. Grahame, 2017, American journal of medical genetics. Part C, Seminars in medical genetics.

Aneurysm-osteoarthritis syndrome with visceral and iliac artery aneurysms.

I. van Herzeele, H. Dietz, J. Roos‐Hesselink, 2013, Journal of vascular surgery.

Congenital heart disease in the ESC EORP Registry of Pregnancy and Cardiac disease (ROPAC)

Prague, K. Sliwa, A. Dirir, 2021 .

Pregnancy Outcomes in Women After Arterial Switch Operation for Transposition of the Great Arteries: Results From ROPAC (Registry of Pregnancy and Cardiac Disease) of the European Society of Cardiology EURObservational Research Programme

K. Sliwa, A. Dirir, S. Blankenberg, 2020, Journal of the American Heart Association.

QRS Duration During Follow-Up of Tetralogy of Fallot: How Valuable is it? Analysis of ECG Changes in Relation to Pulmonary Valve Implantation

L. Demulier, J. De Backer, T. Bové, 2021, Pediatric Cardiology.

Iron deficiency is associated with adverse outcome in Eisenmenger patients.

M. de Pauw, W. Budts, R. Naeije, 2011, European heart journal.

Reply: More Genes for Thoracic Aortic Aneurysms and Dissections.

D. Milewicz, J. De Backer, M. Renard, 2019, Journal of the American College of Cardiology.

Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections.

A. De Paepe, B. Callewaert, P. Coucke, 2015, Current pharmaceutical design.

Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome

P. Byers, X. Jeunemaître, J. Belmont, 2017, American journal of medical genetics. Part C, Seminars in medical genetics.

Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria

A. De Paepe, B. Callewaert, P. Coucke, 2012, Human mutation.

Hepatic Changes in the Fontan Circulation: Identification of Liver Dysfunction and an Attempt to Streamline Follow-up Screening

H. Van Vlierberghe, J. De Backer, A. Geerts, 2018, Pediatric Cardiology.

Successful alcohol septal ablation for late recurrence of left ventricular outflow tract obstruction after surgical myectomy in hypertrophic obstructive cardiomyopathy

D. Devos, J. De Backer, F. Tromp, 2008, Acta cardiologica.

MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking Water

N. Debunne, F. Verbeke, E. Wynendaele, 2020, Frontiers in Pharmacology.

Clinical History and Management Recommendations of the Smooth Muscle Dysfunction Syndrome Due to ACTA2 Arginine 179 Alterations

M. Tekin, B. Lorenz, D. Milewicz, 2018, Genetics in Medicine.

A different view on predictors of pulmonary hypertension in secundum atrial septal defect.

W. Budts, B. Paelinck, J. De Backer, 2014, International journal of cardiology.

Hungarian Marfan family with large FBN1 deletion calls attention to copy number variation detection in the current NGS era.

B. Merkely, M. Pólos, A. M. Kopps, 2018, Journal of thoracic disease.

Questioning the Pathogenic Role of the GLA p.Ala143Thr "Mutation" in Fabry Disease: Implications for Screening Studies and ERT.

W. van Biesen, R. Vanholder, B. Poppe, 2012, JIMD reports.

Right ventricular function in patients with Eisenmenger syndrome.

J. Voigt, M. de Pauw, W. Budts, 2012, The American journal of cardiology.

Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease.

S. Lemaire, R. Jeremy, D. Milewicz, 2022, Journal of the American College of Cardiology.

DUP25 remains unconfirmed

F. Speleman, B. Menten, A. De Paepe, 2004, American journal of medical genetics. Part A.

Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN).

M. Kempers, A. Baas, B. Loeys, 2022, European journal of medical genetics.

Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndrome

A. De Paepe, B. Loeys, B. Callewaert, 2010, Clinical dysmorphology.

Expanding the phenotype of sudden cardiac death-An unusual presentation of a family with a Lamin A/C mutation.

B. Loeys, M. Duytschaever, J. De Backer, 2010, International journal of cardiology.

The ESC Clinical Practice Guidelines for the Management of Adult Congenital Heart Disease 2020.

H. Baumgartner, J. De Backer, 2020, European heart journal.

HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD) a statement from the HTAD working group of VASCERN.

J. Timmermans, M. Groenink, A. Evangelista, 2022, European journal of medical genetics.

Resolving in-vivo flow fields in the systemic circulation of the mouse through combined ultrasound imaging and computational fluid dynamics

P. Segers, B. Loeys, B. Trachet, 2010, 2010 IEEE International Ultrasonics Symposium.

The revised Ghent nosology for the Marfan syndrome

Laurence Faivre, Paul Wordsworth, Richard B Devereux, 2010, Journal of Medical Genetics.

Atenolol versus losartan in children and young adults with Marfan's syndrome.

S. Colan, S. B. Wechsler, H. Dietz, 2014, The New England journal of medicine.

Needs and experiences of adolescents with congenital heart disease and parents in the transitional process: A qualitative study.

D. De Wolf, A. Van Hecke, J. De Backer, 2021, Journal of pediatric nursing.

Aneurysm syndromes caused by mutations in the TGF-beta receptor.

P. Byers, D. Milewicz, H. Dietz, 2006, The New England journal of medicine.

Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions

A. De Paepe, B. Loeys, B. Callewaert, 2008, Genesis.

Effects of age, gender, and left ventricular mass on septal mitral annulus velocity (E') and the ratio of transmitral early peak velocity to E' (E/E').

J. De Sutter, M. D. De Buyzere, T. Gillebert, 2005, The American journal of cardiology.

2020 ESC Guidelines for the management of adult congenital heart disease.

M. Schwerzmann, J. Kluin, K. Zeppenfeld, 2020, European heart journal.

Features of Marfan syndrome not listed in the Ghent nosology – the dark side of the disease

R. Pyeritz, S. Morris, E. Neptune, 2019, Expert review of cardiovascular therapy.

Strain rate imaging detects early cardiac effects of pegylated liposomal Doxorubicin as adjuvant therapy in elderly patients with breast cancer.

F. Rademakers, J. D’hooge, J. Voigt, 2008, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

Opinions of general and adult congenital heart disease cardiologists on care for adults with congenital heart disease in Belgium: a qualitative study

L. Annemans, J. De Backer, R. Willems, 2019, Cardiology in the Young.

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.

Paul Coucke, Marjolijn Renard, Bart Loeys, 2013, International journal of cardiology.

Genes in thoracic aortic aneurysms/dissections - do they matter?

A. De Paepe, J. De Backer, L. Campens, 2013, Annals of cardiothoracic surgery.

The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome

P. Robinson, S. Blankenberg, J. Schmidtke, 2014, Orphanet Journal of Rare Diseases.

Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study.

M Claustres, C Binquet, E. Arbustini, 2007, American journal of human genetics.

A Genotype-First Approach to Exploring Mendelian Cardiovascular Traits with Clear External Manifestations

R. Do, B. Gelb, M. Tartaglia, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Myocardial disease and ventricular arrhythmia in Marfan syndrome: a prospective study

L. Jordaens, D. De Wolf, D. Devos, 2020, Orphanet Journal of Rare Diseases.

Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome

L. Jordaens, D. De Wolf, K. Dhondt, 2019, Molecular genetics & genomic medicine.

Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families

S. Nik-Zainal, K. Devriendt, R. Hennekam, 2008, Human mutation.

An Overview of Investigational and Experimental Drug Treatment Strategies for Marfan Syndrome

P. Sips, J. De Backer, Violette Deleeuw, 2021, Journal of experimental pharmacology.

Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion

E. Arbustini, U. Francke, C. Béroud, 2009, American journal of medical genetics. Part A.

SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections

D. Nickerson, J. Coselli, S. Lemaire, 2019, European Journal of Human Genetics.

Long-Term Outcome of Patients with Perimembranous Ventricular Septal Defect: Results from the Belgian Registry on Adult Congenital Heart Disease

W. Budts, B. Paelinck, J. De Backer, 2016, Cardiology.

FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders.

D. Keene, L. Sakai, J. De Backer, 2016, Gene.

Predictive model for late atrial arrhythmia after closure of an atrial septal defect.

Agnes Pasquet, Werner Budts, Philip Moons, 2013, International journal of cardiology.

Marfan syndrome

D. Milewicz, A. Evangelista, G. Jondeau, 2021, Nature Reviews Disease Primers.

Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndrome

A. De Paepe, B. Loeys, P. Coucke, 2007, Clinical genetics.

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

A. Zwinderman, E. Arbustini, S. Neubauer, 2015, American heart journal.

Last year of life of adults with congenital heart diseases: causes of death and patterns of care

W. Budts, L. Annemans, P. Moons, 2022, European heart journal.

Characterization of Cardiovascular Involvement in Pseudoxanthoma Elasticum Families

P. Segers, T. D. de Backer, A. De Paepe, 2013, Arteriosclerosis, thrombosis, and vascular biology.

In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndrome.

P. Robinson, E. Arbustini, C. Béroud, 2012, American journal of human genetics.

A pilot study to investigate the feasibility and cardiac effects of pegylated liposomal doxorubicin (PL-DOX) as adjuvant therapy in medically fit elderly breast cancer patients.

P. Neven, F. Rademakers, J. Voigt, 2008, Critical reviews in oncology/hematology.

Short-term systolic and diastolic ventricular performance after surgical ventricular restoration for dilated ischemic cardiomyopathy.

M. de Pauw, J. De Backer, T. Bové, 2009, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

The use of Tissue Doppler Imaging for the assessment of changes in myocardial structure and function in inherited cardiomyopathies.

J. De Sutter, D. Matthys, T. Gillebert, 2005, European journal of echocardiography : the journal of the Working Group on Echocardiography of the European Society of Cardiology.

Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome

J. Redondo, D. Milewicz, A. Evangelista, 2017, Nature Medicine.

Parameters of inflammation and infection in a community based case-control study of coronary heart disease.

D. De Bacquer, M. Kornitzer, D. Bacquer, 2002, Atherosclerosis.

The Ghent Marfan Trial--a randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockers.

E. Goetghebeur, C. Vervaet, P. Segers, 2012, International journal of cardiology.

Body mass index in adults with congenital heart disease.

D. De Wolf, S. De Henauw, N. Michels, 2019, Congenital heart disease.

Different levels of care for follow-up of adults with congenital heart disease: a cost analysis scrutinizing the impact on medical costs, hospitalizations, and emergency department visits

A. Marelli, W. Budts, L. Annemans, 2021, The European Journal of Health Economics.

Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials

S. Neubauer, M. Flather, M. Groenink, 2022, The Lancet.

The Application of Clinical Genetics Dovepress Perspectives on the Revised Ghent Criteria for the Diagnosis of Marfan Syndrome

P. Robinson, S. Blankenberg, A. Bernhardt, 2022 .

Primary impairment of left ventricular function in Marfan syndrome.

Patrick Segers, Dirk Matthys, Daniel Devos, 2006, International journal of cardiology.

Managing aortic aneurysms and dissections during pregnancy

J. De Backer, L. Muiño Mosquera, 2015, Expert review of cardiovascular therapy.

Arterial tortuosity syndrome: 40 new families and literature review

K. Devriendt, K. Prescott, H. Dietz, 2018, Genetics in Medicine.

2020 ESC Guidelines for themanagement of adult congenital heart disease

M. Schwerzmann, K. Zeppenfeld, B. Mulder, 2021, Russian Journal of Cardiology.

Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome.

J. Osinga, G. Pals, J. Timmermans, 2014, Gene.

Evaluation of left ventricular dimensions and function in Marfan's syndrome without significant valvular regurgitation.

J. Timmermans, M. P. van den Berg, B. Mulder, 2005, The American journal of cardiology.

Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO

J. Redondo, A. Evangelista, E. Bonzón-Kulichenko, 2021, Nature Communications.

Pregnancy outcome in thoracic aortic disease data from the Registry Of Pregnancy And Cardiac disease

R. Hall, J. Roos‐Hesselink, G. Jondeau, 2021, Heart.

Looking for the Missing Links: Challenges in the Search for Genotype-Phenotype Correlation in Marfan Syndrome.

J. De Backer, L. Campens, L. Muiño Mosquera, 2018, Circulation. Genomic and precision medicine.

Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review

J. De Backer, Y. von Kodolitsch, A. Demolder, 2020, Diagnostics.

Influence of Aortic Stiffness on Aortic-Root Growth Rate and Outcome in Patients With the Marfan Syndrome.

S. Colan, L. Sleeper, G. Pearson, 2018, The American journal of cardiology.

The importance of pulmonary artery pressures on late atrial arrhythmia in transcatheter and surgically closed ASD type secundum.

W. Budts, B. Paelinck, J. De Backer, 2011, International journal of cardiology.

Vessel wall tracking based on the modified autocorrelation estimator

J. De Sutter, P. Verdonck, P. Segers, 2002, 2002 IEEE Ultrasonics Symposium, 2002. Proceedings..

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm

M. Gross, K. Sekiguchi, D. Milewicz, 2020, Genetics in Medicine.

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm

M. Gross, K. Sekiguchi, D. Milewicz, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Genetics in congenital heart disease. Are we ready for it?

B. Callewaert, J. De Backer, L. Muiño Mosquera, 2020, Revista espanola de cardiologia.

Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans

J. De Sutter, P. Segers, A. De Paepe, 2015, Pediatric Research.

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys‐Dietz syndromes

B. Menten, J. Hellemans, A. De Paepe, 2011, Human mutation.

A heart for fibrillin: spatial arrangement in adult wild-type murine myocardial tissue

P. Sips, J. De Backer, J. van Hengel, 2018, Histochemistry and Cell Biology.

Shedding Light on Type B Aortic Dissection in Marfan Syndrome: Implications for Patient Counseling and Research Priorities.

I. van Herzeele, J. De Backer, L. M. Mosquera, 2023, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Functional analysis of the anatomical right ventricular components: should assessment of right ventricular function after repair of tetralogy of Fallot be refined?

Joseph Panzer, Daniel Devos, D. De Wolf, 2014, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stage.

E. Goossens, J. De Backer, K. De Groote, 2022, European journal of pediatrics.

Arterial tortuosity syndrome: 40 new families and literature review

K. Devriendt, K. Prescott, H. Dietz, 2017, Genetics in Medicine.

Corrosion casting of the cardiovascular structure in adult zebrafish for analysis by scanning electron microscopy and X‐ray microtomography

P. Segers, M. Boone, P. Sips, 2020, Anatomia, histologia, embryologia.

Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor

George H. Thomas, Julie De Backer, Paul Coucke, 2006 .

The Application of Clinical Genetics Dovepress Perspectives on the Revised Ghent Criteria for the Diagnosis of Marfan Syndrome

P. Robinson, S. Blankenberg, A. Bernhardt, 2022 .

Reply: ‘Comment on Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors'

G. Burell, M. Perk, J. Burggraaf, 2013, British Journal of Cancer.