prof. dr. Laura Muiño Mosquera

Journal Article
A1
open access

Human stem cell models for Marfan syndrome : a brief overview of the rising star in disease modelling

Jeffrey Aalders (UGent) , Laura Muiño Mosquera (UGent) and Jolanda van Hengel (UGent)

(2025) FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY. 12.

A European Delphi consensus on the management of abdominal aortic aneurysms in patients with heritable aortic diseases

Daniel Gil-Sala, Julie De Backer (UGent) , Isabelle Van Herzeele (UGent) , Gisela Teixidó-Tura, Anders Wanhainen, Sergi Bellmunt-Montoya, Nathalie Moreels (UGent) , Laura Muiño Mosquera (UGent) , Liesbeth Wildero - Van Wouwe (UGent) and [missing] Consensus Participants

(2025) EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY.

Add to list

Miscellaneous

Beyond the usual suspects : autosomal recessive forms of childhood-onset thoracic aortic disease

Simon D'hulst (UGent) and Laura Muiño Mosquera (UGent)

(2025) INTERNATIONAL JOURNAL OF CARDIOLOGY. 421.

Add to list

Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease : results from the Montalcino Aortic Consortium

Michelle Su-Anne Lim, Dong-Chuan Guo, Walter Velasco Torrez, Andrew Lai, Jonathan Schweber, Nikita Garg, Julie Fleischer, Catherine Boileau, Julie De Backer (UGent) , Artur Evangelista, et al.

(2025) JOURNAL OF MEDICAL GENETICS. 62(2). p.82-88

Add to list

Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource’s FBN1 variant curation expert panel

A. Drackley, C. Somerville, P. Arnaud, L. M. Baudhuin, N. Hanna, M. L. Kluge, K. Kotzer, C. Boileau, L. Bronicki, Bert Callewaert (UGent) , et al.

(2024) GENOME MEDICINE. 16(1).

Add to list

Journal Article
A1
open access

New insights into the structural role of EMILINs within the human skin microenvironment

Alvise Schiavinato, Fady Marcous, Alexandra V. Zuk, Douglas R. Keene, Sara F. Tufa, Laura Muiño Mosquera (UGent) , Paola Zigrino, Cornelia Mauch, Beate Eckes, Katrien Francois (UGent) , et al.

(2024) SCIENTIFIC REPORTS. 14(1).

Add to list

Unraveling Marfan hearts : ultrastructural evidence for myocardial remodeling and cardiomyopathy

Violette Deleeuw (UGent) , Simon D'hulst (UGent) , Anthony Demolder (UGent) , Felke Steijns, Marjolijn Renard (UGent) , Riet De Rycke (UGent) , Jo Van Dorpe (UGent) , Laura Muiño Mosquera (UGent) , Katrien Francois (UGent) , Kálmán Benke, et al.

(2024) EUROPEAN HEART JOURNAL. In European Heart Journal 45(Supplement 1).

Add to list

Mitral valve phenotypes in SMAD3-related thoracic aortic disease : insights from the Montalcino Aortic Consortium

S K Prakash, K L Asokan, Wannes Renders (UGent) , Laura Muiño Mosquera (UGent) , Julie De Backer (UGent) , D Jantzen, A T Yetman, G Teixido-Tura, R Jeremy, E G Jones, et al.

(2024) EUROPEAN HEART JOURNAL. In European Heart Journal 45(Supplement 1).

Add to list

Journal Article
A1
open access

Mitral annular disjunction in heritable thoracic aortic disease : insights from the Montalcino Aortic Consortium

Kishan L Asokan, Jennifer R Landes, Wannes Renders (UGent) , Laura Muiño Mosquera (UGent) , Julie De Backer (UGent) , David W Jantzen, Anji T Yetman, Gisela Teixido-Tura, Arturo Evangelista, Richmond Jeremy, et al.

(2024) JOURNAL OF THE AMERICAN HEART ASSOCIATION. 13(21).

Add to list

Journal Article
A1
open access

Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

Steven G. Carlisle, Hasan Albasha, Hector I. Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer (UGent) , Laura Muiño Mosquera (UGent) , Anji T. Yetman, Malenka M. Bissell, Maria Grazia Andreassi, et al.

(2024) PLOS ONE. 19(9).

Academic Bibliography

prof. dr. Laura Muiño Mosquera

Human stem cell models for Marfan syndrome : a brief overview of the rising star in disease modelling

A European Delphi consensus on the management of abdominal aortic aneurysms in patients with heritable aortic diseases

Beyond the usual suspects : autosomal recessive forms of childhood-onset thoracic aortic disease

Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease : results from the Montalcino Aortic Consortium

Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource’s FBN1 variant curation expert panel

New insights into the structural role of EMILINs within the human skin microenvironment

Unraveling Marfan hearts : ultrastructural evidence for myocardial remodeling and cardiomyopathy

Mitral valve phenotypes in SMAD3-related thoracic aortic disease : insights from the Montalcino Aortic Consortium

Mitral annular disjunction in heritable thoracic aortic disease : insights from the Montalcino Aortic Consortium

Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve

Contents

Support

Contact