Julie De Backer

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 31

Top Topics

Congenital Heart Disease

Top Venues

medRxiv : the preprint server for health sciences

European journal of human genetics : EJHG

Journal of cardiovascular development and disease

European heart journal

This page only lists publications with an associated author ORCID identifier.

Publications

Maximilian A Selbst, Megan K Laughlin, Colin R Ward, Hector Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dongchuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Shaine A Morris, Kim L McBride, Simon C Body, null null, Siddharth K Prakash
Bicuspid Aortic Valve Disease With Early Onset Complications: Characteristics And Aortic Outcomes. medRxiv : the preprint server for health sciences (2024)
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG 32 (9) (2024)
Maximilian A Selbst, Megan K Laughlin, Colin R Ward, Hector Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dongchuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Shaine A Morris, Kim L McBride, Simon C Body, null null, Siddharth K Prakash
Bicuspid Aortic Valve Disease With Early Onset Complications: Characteristics And Aortic Outcomes. medRxiv : the preprint server for health sciences (2024)
Steven G Carlisle, Hasan Albasha, Hector I Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dongchuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Kim L McBride, Dianna M Milewicz, Simon C Body, Siddharth K Prakash, null null, null null
Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve. PloS one 19 (9) (2024)
Maximilian A Selbst, Megan K Laughlin, Colin R Ward, Hector Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dongchuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Shaine A Morris, Kim L McBride, Simon C Body, null null, Siddharth K Prakash
Bicuspid Aortic Valve Disease With Early Onset Complications: Characteristics And Aortic Outcomes. medRxiv : the preprint server for health sciences (2024)
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG (2024)
Lucia Mazzolai, Gisela Teixidó, Stefano Lanzi, Vinko Boc, Eduardo Bossone, Marianne Brodmann, Alessandra Bura Rivière, Julie De Backer, Sebastien Deglise, Alessandro Della Corte, Christian Heiss, Marta Kaluzna-Oleksy, Donata Kurpas, Carmel M McEniery, Tristan Mirault, Agnes A Pasquet, Alex Pitcher, Hannah A I Schaubroeck, Oliver Schlager, Per Anton Sirnes, Muriel G Sprynger, Eugenio Stabile, Françoise Steinbach, Matthias Thielmann, Roland R J van Kimmenade, Maarit A Venermo, José F Rodriguez Palomares, null null
2024 ESC Guidelines for the management of peripheral arterial and aortic diseases. European heart journal (2024)
Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen B M Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende, Tessi Beyltjens, Eleanor R Scimone, Mark E Lindsay, Lisa A Schimmenti, Alicia M Hinze, Emily Dunn, Natalia Gomez-Ospina, Isabelle Vandernoot, Thomas Delguste, Sandra Coppens, Valerie Cormier-Daire, Tartaglia Marco, Livia Garavelli, Joseph T C Shieh, Şenol Demir, Esra Arslan Ates, Martin Zenker, Mersedeh Rohanizadegan, Greysha Rivera-Cruz, Sofia Douzgou Houge, null null, Angela E Lin, Bert Callewaert
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations. European journal of human genetics : EJHG (2024)
Michèle de Hosson, Katya De Groote, Herlinde Wynendaele, Laura Muiño Mosquera, Eva Goossens, Julie De Backer
Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stage. European journal of pediatrics (2023)
Steven G Carlisle, Hasan Albasha, Hector Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dong-Chuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Kim L McBride, null null, null null, Dianna M Milewicz, Simon C Body, Siddharth K Prakash
Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve. medRxiv : the preprint server for health sciences (2023)
Tijs K Tournoy, Philip Moons, Bo Daelman, Julie De Backer
Biological Age in Congenital Heart Disease-Exploring the Ticking Clock. Journal of cardiovascular development and disease 10 (12) (2023)
Julie De Backer, Siddharth K Prakash
Refining the course: long-term outcome in patients with bicuspid aortic valve. European heart journal (2023)
Julie De Backer, Laura Muiño Mosquera
Genetic Testing in Patients With Congenital Heart Disease: You Do No Harm When Using the Right Tools! Circulation. Genomic and precision medicine (2023)
Tijs K Tournoy, Philip Moons, Bo Daelman, Julie De Backer
Biological Age in Congenital Heart Disease-Exploring the Ticking Clock. Journal of cardiovascular development and disease 10 (12) (2023)
Tijs K Tournoy, Philip Moons, Bo Daelman, Julie De Backer
Biological Age in Congenital Heart Disease-Exploring the Ticking Clock. Journal of cardiovascular development and disease 10 (12) (2023)
Jonas Verbeke, Anthony Demolder, Julie De Backer, Frank Timmermans
Mitral Annular Disjunction: Associated Pathologies and Clinical Consequences. Current cardiology reports (2022)
Liesbet Van Bulck, Eva Goossens, Lucas Morin, Koen Luyckx, Fouke Ombelet, Ruben Willems, Werner Budts, Katya De Groote, Julie De Backer, Lieven Annemans, Stéphane Moniotte, Michèle de Hosson, Arianne Marelli, Philip Moons, null null
Last year of life of adults with congenital heart diseases: causes of death and patterns of care. European heart journal 43 (42) (2022)
Thomas Martens, Katrien François, Hans De Wilde, Laurence Campens, Laurent Demulier, Julie De Backer, Daniël De Wolf, Thierry Bove
QRS Duration During Follow-Up of Tetralogy of Fallot: How Valuable is it? Analysis of ECG Changes in Relation to Pulmonary Valve Implantation. Pediatric cardiology 42 (7) (2021)
Violette Deleeuw, Adelbert De Clercq, Julie De Backer, Patrick Y Sips
An Overview of Investigational and Experimental Drug Treatment Strategies for Marfan Syndrome. Journal of experimental pharmacology 13 (2021)
Laurence Campens, Lucia Baris, Nandita S Scott, Craig S Broberg, Antione Bondue, Guillaume Jondeau, Jasmine Grewal, Mark R Johnson, Roger Hall, Julie De Backer, Jolien W Roos-Hesselink, null null
Pregnancy outcome in thoracic aortic disease data from the Registry Of Pregnancy And Cardiac disease. Heart (British Cardiac Society) 107 (21) (2021)
Andrea de la Fuente-Alonso, Marta Toral, Alvaro Alfayate, María Jesús Ruiz-Rodríguez, Elena Bonzón-Kulichenko, Gisela Teixidó, Sara Martínez-Martínez, María José Méndez-Olivares, Dolores López-Maderuelo, Ileana González-Valdés, Eusebio Garcia-Izquierdo, Susana Mingo, Carlos E Martín, Laura Muiño-Mosquera, Julie De Backer, J Francisco Nistal, Alberto Forteza, Arturo Evangelista, Jesus Vazquez, Miguel R Campanero, Juan Miguel Redondo
Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO. Nature communications 12 (1) (2021)
Felke Steijns, Máté I Tóth, Anthony Demolder, Lars E Larsen, Jana Desloovere, Marjolijn Renard, Robrecht Raedt, Patrick Segers, Julie De Backer, Patrick Y Sips
Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious Mice. Sensors (Basel, Switzerland) 20 (14) (2020)
Felke Steijns, Marjolijn Renard, Marine Vanhomwegen, Petra Vermassen, Jana Desloovere, Robrecht Raedt, Lars E Larsen, Máté I Tóth, Julie De Backer, Patrick Y Sips
Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome. International journal of molecular sciences 21 (19) (2020)
Anthony Demolder, Yskert von Kodolitsch, Laura Muiño Mosquera, Julie De Backer
Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review. Diagnostics (Basel, Switzerland) 10 (10) (2020)
Kristina Mühlstädt, Julie De Backer, Yskert von Kodolitsch, Kerstin Kutsche, Laura Muiño Mosquera, Jens Brickwedel, Evaldas Girdauskas, Thomas S Mir, Adrian Mahlmann, Nikolaos Tsilimparis, Axel Staebler, Lauritz Schoof, Heide Seidel, Jürgen Berger, Alexander M Bernhardt, Stefan Blankenberg, Tilo Kölbel, Christian Detter, Katalin Szöcs, Harald Kaemmerer
Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome. Journal of clinical medicine 8 (12) (2019)
Laura Muiño Mosquera, Fré Bauters, Karlien Dhondt, Hans De Wilde, Luc Jordaens, Katya De Groote, Daniel De Wolf, Katrien Hertegonne, Julie De Backer
Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome. Molecular genetics & genomic medicine 7 (8) (2019)
Mahmoud Zaqout, Kristof Vandekerckhove, Nathalie Michels, Laurent Demulier, Thierry Bove, Katrien François, Julie De Backer, Stefaan De Henauw, Daniel De Wolf
Body mass index in adults with congenital heart disease. Congenital heart disease 14 (3) (2019)
Xue-Yan Duan, Dong-Chuan Guo, Ellen S Regalado, Hong Shen, null null, Joseph S Coselli, Anthony L Estrera, Hazim J Safi, Michael J Bamshad, Deborah A Nickerson, Scott A LeMaire, Julie De Backer, Dianna M Milewicz
SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections. European journal of human genetics : EJHG 27 (7) (2019)
Julie De Backer, Alan C Braverman
Heart failure and sudden cardiac death in heritable thoracic aortic disease caused by pathogenic variants in the SMAD3 gene. Molecular genetics & genomic medicine (2018)
Jorge Oller, Nerea Méndez-Barbero, E Josue Ruiz, Silvia Villahoz, Marjolijn Renard, Lizet I Canelas, Ana M Briones, Rut Alberca, Noelia Lozano-Vidal, María A Hurlé, Dianna Milewicz, Arturo Evangelista, Mercedes Salaices, J Francisco Nistal, Luis Jesús Jiménez-Borreguero, Julie De Backer, Miguel R Campanero, Juan Miguel Redondo
Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome. Nature medicine 23 (2) (2017)
Laurence Campens, Marjolijn Renard, Bram Trachet, Patrick Segers, Laura Muino Mosquera, Johan De Sutter, Lynn Sakai, Anne De Paepe, Julie De Backer
Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans. Pediatric research 78 (3) (2015)