prof. dr. Laura Muiño Mosquera

Filamin C associated cardiomyopathy in pediatric patients : a Belgian case series and literature review

Wannes Renders (UGent) , Evelien Cansse (UGent) , Luc Bruyndonckx, Thomas Salaets, Bert Callewaert (UGent) , Katya De Groote (UGent) and Laura Muiño Mosquera (UGent)

(2025) BELGIAN JOURNAL OF PAEDIATRICS. In Belgian Journal of Paediatrics p.62-62

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Genetic background of patients with childhood-onset cardiomyopathy : results from a retrospective cohort study

Wannes Renders (UGent) , Evelien Cansse (UGent) , Max Bascialli, Joseph Panzer (UGent) , Hans De Wilde (UGent) , Kristof Vandekerckhove (UGent) , Bert Callewaert (UGent) , Arnaud Vanlander (UGent) , Katya De Groote (UGent) , Daniël De Wolf (UGent) , et al.

(2025) BELGIAN JOURNAL OF PAEDIATRICS. p.67-67

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Novel aortic dissection model links endothelial dysfunction and immune infiltration

Kenichi Kimura, Eri Motoyama, Sachiko Kanki, Keiichi Asano, Patrick Sips (UGent) , Md Al Amin Sheikh, Maria Thea Rane Dela Cruz Clarin, Erna Raja, Mariko Takeda, Ryutaro Ishii, et al.

(2025) CIRCULATION RESEARCH. 137(1). p.26-42

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open access

RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease

Maxim Verlee (UGent) , Erika D'haenens (UGent) , Laurenz De Cock, Laura Muiño Mosquera (UGent) , Katya De Groote (UGent) , Kristof Vandekerckhove (UGent) , Joseph Panzer (UGent) , Ellen Roets (UGent) , Björn Menten (UGent) , Sofie Symoens (UGent) , et al.

(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. 33(8). p.1085-1089

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Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve

Helene DiGregorio, Sara Mansoorshahi, Steven G Carlisle, Catherina Tovar Pensa, Abi Watts, Courtney McNeely, Anna Sabate-Rotes, Anji Yetman, Hector I Michelena, Julie De Backer (UGent) , et al.

(2025) HEART. 111(5). p.221-229

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Genes associated with hypertrophic cardiomyopathy : a reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel

Sophie Hespe, Amber Waddell, Babken Asatryan, Emma Owens, Courtney Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily E. Brown, Lily Hoffman-Andrews, Elizabeth Jordan, et al.

(2025) JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. 85(7). p.727-740

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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.

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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. 69(5). p.723-731

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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.

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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

Academic Bibliography

prof. dr. Laura Muiño Mosquera

Filamin C associated cardiomyopathy in pediatric patients : a Belgian case series and literature review

Genetic background of patients with childhood-onset cardiomyopathy : results from a retrospective cohort study

Novel aortic dissection model links endothelial dysfunction and immune infiltration

RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease

Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve

Genes associated with hypertrophic cardiomyopathy : a reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel

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

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