Ilse Luyckx

778 total citations
14 papers, 232 citations indexed

About

Ilse Luyckx is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Ilse Luyckx has authored 14 papers receiving a total of 232 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Pulmonary and Respiratory Medicine and 3 papers in Molecular Biology. Recurrent topics in Ilse Luyckx's work include Connective tissue disorders research (11 papers), Aortic aneurysm repair treatments (7 papers) and Aortic Disease and Treatment Approaches (6 papers). Ilse Luyckx is often cited by papers focused on Connective tissue disorders research (11 papers), Aortic aneurysm repair treatments (7 papers) and Aortic Disease and Treatment Approaches (6 papers). Ilse Luyckx collaborates with scholars based in Belgium, Netherlands and United Kingdom. Ilse Luyckx's co-authors include Bart Loeys, Aline Verstraeten, Lut Van Laer, Harry C. Dietz, Josephina Meester, Marie‐José Goumans, Geert Mortier, Meena Balasubramanian, Hiroko Morisaki and Inez Rodrigus and has published in prestigious journals such as International Journal of Molecular Sciences, The American Journal of Human Genetics and Bone.

In The Last Decade

Ilse Luyckx

13 papers receiving 229 citations

Peers

Ilse Luyckx

PRM

GENET

CCM

SURGE

H. Pannu United States

Maud Langeois France

Ludivine Eliahou France

Alex R. Dalal United States

Victoria Cañadas Spain

Rocío Mena Spain

Guoyan Zhu China

Bo Wen Cai China

Salma Adham France

Min‐Lee Yang United States

H. Pannu United States

Ilse Luyckx

269 ×1.9

PRM

240 ×2.0

GENET

102 ×1.6

CCM

78 ×1.4

58 ×1.4

SURGE

Citations per year, relative to Ilse Luyckx Ilse Luyckx (= 1×) peers H. Pannu

Countries citing papers authored by Ilse Luyckx

Since Specialization

Citations

This map shows the geographic impact of Ilse Luyckx's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ilse Luyckx with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ilse Luyckx more than expected).

Fields of papers citing papers by Ilse Luyckx

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ilse Luyckx. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ilse Luyckx. The network helps show where Ilse Luyckx may publish in the future.

Co-authorship network of co-authors of Ilse Luyckx

This figure shows the co-authorship network connecting the top 25 collaborators of Ilse Luyckx. A scholar is included among the top collaborators of Ilse Luyckx based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ilse Luyckx. Ilse Luyckx is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

Richer, Julie, Sharan Goobie, Ingrid M.B.H. van de Laar, et al.. (2025). Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals. Journal of Medical Genetics. 62(3). 199–205.

Luyckx, Ilse, Nele Boeckx, Kristof Van Schil, et al.. (2024). Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of Medical Genetics. 61(4). 363–368. 2 indexed citations

Verstraeten, Aline, Ilse Luyckx, A.H. Jan Danser, et al.. (2024). 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). 5025–5025. 1 indexed citations

Laga, Steven, Inge Goovaerts, Johan Saenen, et al.. (2023). Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier. Frontiers in Genetics. 14. 1251675–1251675. 1 indexed citations

Krebsová, Alice, Ilse Luyckx, Steven Laga, et al.. (2022). Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants. Human Mutation. 43(12). 1824–1828. 5 indexed citations

Luyckx, Ilse, Aline Verstraeten, Marie‐José Goumans, & Bart Loeys. (2022). SMAD6-deficiency in human genetic disorders. npj Genomic Medicine. 7(1). 68–68. 14 indexed citations

Meester, Josephina, et al.. (2022). The Genetics and Typical Traits of Thoracic Aortic Aneurysm and Dissection. Annual Review of Genomics and Human Genetics. 23(1). 223–253. 32 indexed citations

Laer, Lut Van, et al.. (2021). Loeys-Dietz Syndrome. Advances in experimental medicine and biology. 251–264. 29 indexed citations

Krebsová, Alice, Birgitte Rode Diness, Steven Laga, et al.. (2021). Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings. International Journal of Molecular Sciences. 22(13). 7111–7111. 9 indexed citations

10.

Alaerts, Maaike, Gerarda van de Beek, Ilse Luyckx, et al.. (2019). Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool. Frontiers in Medicine. 6. 198–198. 1 indexed citations

11.

Balasubramanian, Meena, Ilse Luyckx, Geert Mortier, et al.. (2019). Aortic aneurysm/dissection and osteogenesis imperfecta: Four new families and review of the literature. Bone. 121. 191–195. 19 indexed citations

12.

Boudin, Eveline, Timothy C. R. Prickett, Bruno Lapauw, et al.. (2018). Bi-allelic Loss-of-Function Mutations in the NPR-C Receptor Result in Enhanced Growth and Connective Tissue Abnormalities. The American Journal of Human Genetics. 103(2). 288–295. 25 indexed citations

13.

Verstraeten, Aline, Ilse Luyckx, & Bart Loeys. (2017). Aetiology and management of hereditary aortopathy. Nature Reviews Cardiology. 14(4). 197–208. 75 indexed citations

14.

Luyckx, Ilse & Bart Loeys. (2015). The genetic architecture of non-syndromic thoracic aortic aneurysm. Heart. 101(20). 1678–1684. 19 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact