Genomic Modifiers of Inherited Aortapathy

Project Information

GENOMIA

Grant agreement ID: 771945

DOI

10.3030/771945

Project closed

EC signature date 15 June 2018

Start date 1 January 2019

End date 31 December 2023

Funded under

• EXCELLENT SCIENCE - European Research Council (ERC)

Total cost

€ 1 987 860,00

EU contribution

€ 1 987 860,00

Coordinated by

UNIVERSITEIT ANTWERPEN
Belgium

CORDIS provides links to public deliverables and publications of HORIZON projects.

Links to deliverables and publications from FP7 projects, as well as links to some specific result types such as dataset and software, are dynamically retrieved from OpenAIRE .

Publications

Peer reviewed articles (7)

Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia

Author(s): Alexandre Persu, Piotr Dobrowolski, Heather L Gornik, Jeffrey W Olin, David Adlam, Michel Azizi, Pierre Boutouyrie, Rosa Maria Bruno, Marion Boulanger, Jean-Baptiste Demoulin, Santhi K Ganesh, Tomasz J. Guzik, Magdalena Januszewicz, Jason C Kovacic, Mariusz Kruk, Peter de Leeuw, Bart L Loeys, Marco Pappaccogli, Melanie H A M Perik, Emmanuel Touzé, Patricia Van der Niepen, Daan J L Van Twist, Ewa
Published in: Cardiovascular Research, 2021, ISSN 0008-6363
Publisher: Elsevier BV
DOI: 10.1093/cvr/cvab086

Enrichment of Rare Variants in Loeys–Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia

Author(s): Aline Verstraeten, Melanie H.A.M. Perik, Anna A. Baranowska, Josephina A.N. Meester, Lotte Van Den Heuvel, Jarl Bastianen, Marlies Kempers, Ingrid P.C. Krapels, Angela Maas, Andrea Rideout, Anthony Vandersteen, Glenda Sobey, Diana Johnson, Erik Fransen, Neeti Ghali, Tom Webb, Abtehale Al-Hussaini, Peter de Leeuw, Philippe Delmotte, Marilucy Lopez-Sublet, Marco Pappaccogli, Muriel Sprynger, Laurent
Published in: Circulation, Issue 142/10, 2020, Page(s) 1021-1024, ISSN 0009-7322
Publisher: Lippincott Williams & Wilkins Ltd.
DOI: 10.1161/circulationaha.120.045946

Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing

Author(s): Shalini S. Nayak, Pauline E. Schneeberger, Siddaramappa J. Patil, Karegowda M. Arun, Pujar V. Suresh, Viralam S. Kiran, Sateesh Siddaiah, Shreesha Maiya, Shrikanth K. Venkatachalagupta, Neethukrishna Kausthubham, Fanny Kortüm, Isabella Rau, Alexandra Wey-Fabrizius, Lotte Van Den Heuvel, Josephina Meester, Lut Van Laer, Anju Shukla, Bart Loeys, Katta M. Girisha, Kerstin Kutsche
Published in: Scientific Reports, Issue 11/1, 2021, ISSN 2045-2322
Publisher: Nature Publishing Group
DOI: 10.1038/s41598-020-80755-7

Extracellular Matrix in Vascular Disease, Part 2/4

Author(s): Javier Barallobre-Barreiro, Bart Loeys, Manuel Mayr, Marieke Rienks, Aline Verstraeten, Jason C. Kovacic
Published in: Journal of the American College of Cardiology, Issue 75/17, 2020, Page(s) 2189-2203, ISSN 0735-1097
Publisher: Elsevier BV
DOI: 10.1016/j.jacc.2020.03.018

A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8

Author(s): Ilse Van Gucht, Josephina A.N. Meester, Jotte Rodrigues Bento, Maaike Bastiaansen, Jarl Bastianen, Ilse Luyckx, Lotte Van Den Heuvel, Cédric H.G. Neutel, Pieter-Jan Guns, Mandy Vermont, Erik Fransen, Melanie H.A.M. Perik, Joe Davis Velchev, Maaike Alaerts, Dorien Schepers, Silke Peeters, Isabel Pintelon, Abdulrahman Almesned, Matteo P. Ferla, Jenny C. Taylor, Anthony R. Dallosso, Maggie Williams,
Published in: The American Journal of Human Genetics, Issue 108/6, 2021, Page(s) 1115-1125, ISSN 0002-9297
Publisher: University of Chicago Press
DOI: 10.1016/j.ajhg.2021.04.019

Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool

Author(s): Maaike Alaerts, Gerarda van de Beek, Ilse Luyckx, Josephina Meester, Dorien Schepers, Aline Verstraeten, Johan Saenen, Emeline Van Craenenbroeck, Inge Goovaerts, Inez Rodrigus, Steven Laga, Jeroen Hendriks, Sofie Goethals, Annemieke De Wilde, Elke Smits, Philippe Jorens, Manon Huizing, Lut Van Laer, Bart Loeys
Published in: Frontiers in Medicine, Issue 6, 2019, ISSN 2296-858X
Publisher: Frontiers
DOI: 10.3389/fmed.2019.00198

Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings

Author(s): Ilse Van Gucht, Alice Krebsova, Birgitte Rode Diness, Steven Laga, Dave Adlam, Marlies Kempers, Nilesh J. Samani, Tom R. Webb, Ania A. Baranowska, Lotte Van Den Heuvel, Melanie Perik, Ilse Luyckx, Nils Peeters, Pavel Votypka, Milan Macek, Josephina Meester, Lut Van Laer, Aline Verstraeten, Bart L. Loeys
Published in: International Journal of Molecular Sciences, Issue 22/13, 2021, Page(s) 7111, ISSN 1422-0067
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms22137111