Genomic Modifiers of Inherited Aortapathy

Informazioni relative al progetto

GENOMIA

ID dell’accordo di sovvenzione: 771945

DOI

10.3030/771945

Progetto chiuso

Data della firma CE 15 Giugno 2018

Data di avvio 1 Gennaio 2019

Data di completamento 31 Dicembre 2023

Finanziato da

• EXCELLENT SCIENCE - European Research Council (ERC)

Costo totale

€ 1 987 860,00

Contributo UE

€ 1 987 860,00

Coordinato da

UNIVERSITEIT ANTWERPEN
Belgium

CORDIS fornisce collegamenti ai risultati finali pubblici e alle pubblicazioni dei progetti ORIZZONTE.

I link ai risultati e alle pubblicazioni dei progetti del 7° PQ, così come i link ad alcuni tipi di risultati specifici come dataset e software, sono recuperati dinamicamente da .OpenAIRE .

Pubblicazioni

Peer reviewed articles (7)

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

Autori: 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
Pubblicato in: Cardiovascular Research, 2021, ISSN 0008-6363
Editore: 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

Autori: 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
Pubblicato in: Circulation, Numero 142/10, 2020, Pagina/e 1021-1024, ISSN 0009-7322
Editore: 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

Autori: 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
Pubblicato in: Scientific Reports, Numero 11/1, 2021, ISSN 2045-2322
Editore: Nature Publishing Group
DOI: 10.1038/s41598-020-80755-7

Extracellular Matrix in Vascular Disease, Part 2/4

Autori: Javier Barallobre-Barreiro, Bart Loeys, Manuel Mayr, Marieke Rienks, Aline Verstraeten, Jason C. Kovacic
Pubblicato in: Journal of the American College of Cardiology, Numero 75/17, 2020, Pagina/e 2189-2203, ISSN 0735-1097
Editore: 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

Autori: 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,
Pubblicato in: The American Journal of Human Genetics, Numero 108/6, 2021, Pagina/e 1115-1125, ISSN 0002-9297
Editore: 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

Autori: 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
Pubblicato in: Frontiers in Medicine, Numero 6, 2019, ISSN 2296-858X
Editore: Frontiers
DOI: 10.3389/fmed.2019.00198

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

Autori: 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
Pubblicato in: International Journal of Molecular Sciences, Numero 22/13, 2021, Pagina/e 7111, ISSN 1422-0067
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms22137111