Ilse Luyckx (I Luyckx)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 13

Top Topics

Angiotensin Converting Enzyme

Aortic Aneurysm

Top Venues

Journal of medical genetics

International journal of molecular sciences

NPJ genomic medicine

Nature genetics

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

Publications

Irene Valdivia Callejon, Lucia Buccioli, Jarl Bastianen, Jolien Schippers, Aline Verstraeten, Ilse Luyckx, Silke Peeters, Alexander H J Danser, Roland R J Van Kimmenade, Josephina A N Meester, Bart L Loeys
Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome. International journal of molecular sciences 25 (9) (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)
Irene Valdivia Callejon, Lucia Buccioli, Jarl Bastianen, Jolien Schippers, Aline Verstraeten, Ilse Luyckx, Silke Peeters, Alexander H J Danser, Roland R J Van Kimmenade, Josephina A N Meester, Bart L Loeys
Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome. International journal of molecular sciences 25 (9) (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)
Irene Valdivia Callejon, Lucia Buccioli, Jarl Bastianen, Jolien Schippers, Aline Verstraeten, Ilse Luyckx, Silke Peeters, Alexander H J Danser, Roland R J Van Kimmenade, Josephina A N Meester, Bart L Loeys
Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome. International journal of molecular sciences 25 (9) (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)
Ilse Luyckx, Aline Verstraeten, Marie-José T H Goumans, Bart L Loeys
SMAD6-deficiency in human genetic disorders. NPJ genomic medicine 7 (1) (2022)
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 A N Meester, Lut Van Laer, Aline Verstraeten, Bart L Loeys
Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings. International journal of molecular sciences 22 (13) (2021)
Ilse Luyckx, Ajay A Kumar, Edwin Reyniers, Emily Dekeyser, Kathleen Vanderstraeten, Geert Vandeweyer, Florian Wünnemann, Christoph Preuss, Jean-Michaël Mazzella, Guillaume Goudot, Emmanuel Messas, Juliette Albuisson, Xavier Jeunemaitre, Per Eriksson, Salah A Mohamed, Marlies Kempers, Simone Salemink, Anthonie L Duijnhouwer, Gregor U Andelfinger, Harry C Dietz, Aline Verstraeten, Lut Van Laer, Bart L Loeys, null null
Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene. European journal of human genetics : EJHG 27 (7) (2019)
Russell A Gould, Hamza Aziz, Courtney E Woods, Manuel Alejandro Seman-Senderos, Elizabeth Sparks, Christoph Preuss, Florian Wünnemann, Djahida Bedja, Cassandra R Moats, Sarah A McClymont, Rebecca Rose, Nara Sobreira, Hua Ling, Gretchen MacCarrick, Ajay Anand Kumar, Ilse Luyckx, Elyssa Cannaerts, Aline Verstraeten, Hanna M Björk, Ann-Cathrin Lehsau, Vinod Jaskula-Ranga, Henrik Lauridsen, Asad A Shah, Christopher L Bennett, Patrick T Ellinor, Honghuang Lin, Eric M Isselbacher, Christian L Lino Cardenas, Jonathan T Butcher, G Chad Hughes, Mark E Lindsay, null null, null null, Luc Mertens, Anders Franco-Cereceda, Judith M A Verhagen, Marja Wessels, Salah A Mohamed, Per Eriksson, Seema Mital, Lut Van Laer, Bart L Loeys, Gregor U Andelfinger, Andrew S McCallion, Harry C Dietz
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm. Nature genetics 51 (1) (2018)
Ilse Luyckx, D Proost, J M H Hendriks, J Saenen, E M Van Craenenbroeck, T Vermeulen, N Peeters, W Wuyts, I Rodrigus, A Verstraeten, L Van Laer, B L Loeys
Two novel MYLK nonsense mutations causing thoracic aortic aneurysms/dissections in patients without apparent family history. Clinical genetics 92 (4) (2017)