Aline Verstraeten

2.7k total citations
44 papers, 1.2k citations indexed

About

Aline Verstraeten is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Aline Verstraeten has authored 44 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 22 papers in Pulmonary and Respiratory Medicine and 11 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Aline Verstraeten's work include Connective tissue disorders research (24 papers), Aortic Disease and Treatment Approaches (17 papers) and Aortic aneurysm repair treatments (13 papers). Aline Verstraeten is often cited by papers focused on Connective tissue disorders research (24 papers), Aortic Disease and Treatment Approaches (17 papers) and Aortic aneurysm repair treatments (13 papers). Aline Verstraeten collaborates with scholars based in Belgium, Netherlands and United Kingdom. Aline Verstraeten's co-authors include Bart Loeys, Lut Van Laer, Christine Van Broeckhoven, Jessie Theuns, Maaike Alaerts, Josephina Meester, Dorien Schepers, Ilse Luyckx, Sebastiaan Engelborghs and Manuel Mayr and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the American College of Cardiology and International Journal of Molecular Sciences.

In The Last Decade

Aline Verstraeten

42 papers receiving 1.1k citations

Peers

Aline Verstraeten

GENET

PRM

NEURO

CCM

Marios Kambouris United States

Tatsuo Mima Japan

Emilia Vitale Italy

Daniëlle Majoor‐Krakauer Netherlands

Teresa Esposito Italy

Jon Andoni Urtizberea France

Yuri A. Zárate United States

Satoshi Matsushima Japan

Marco Di Duca Italy

Takashi Miyazawa Japan

Marios Kambouris United States

Aline Verstraeten

430 ×1.0

GENET

286 ×0.8

PRM

436 ×1.3

68 ×0.3

NEURO

117 ×0.6

CCM

Citations per year, relative to Aline Verstraeten Aline Verstraeten (= 1×) peers Marios Kambouris

Countries citing papers authored by Aline Verstraeten

Since Specialization

Citations

This map shows the geographic impact of Aline Verstraeten'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 Aline Verstraeten with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aline Verstraeten more than expected).

Fields of papers citing papers by Aline Verstraeten

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aline Verstraeten. 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 Aline Verstraeten. The network helps show where Aline Verstraeten may publish in the future.

Co-authorship network of co-authors of Aline Verstraeten

This figure shows the co-authorship network connecting the top 25 collaborators of Aline Verstraeten. A scholar is included among the top collaborators of Aline Verstraeten 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 Aline Verstraeten. Aline Verstraeten is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Verstraeten, Aline, et al.. (2023). IPSC-derived vascular smooth muscle cell model recapitulates Loeys-Dietz-Syndrome type V aortic phenotype. European Heart Journal. 44(Supplement_2). 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

Verstraeten, Aline, Josephina Meester, Peter Ponsaerts, et al.. (2022). Generation and validation of an iPSC line (BBANTWi008-A) from a Loeys-Dietz Syndrome type 3 patient. Stem Cell Research. 64. 102932–102932. 2 indexed citations

Verstraeten, Aline, et al.. (2022). Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patient. Stem Cell Research. 65. 102956–102956. 1 indexed citations

Kempers, Marlies, Koenraad Devriendt, Luc De Catte, et al.. (2021). Two novel presentations of KCNMA1‐related pathology––Expanding the clinical phenotype of a rare channelopathy. Molecular Genetics & Genomic Medicine. 9(10). 5 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

Meester, Josephina, Bart Loeys, Elvire Gouze, et al.. (2020). Differentiation of Induced Pluripotent Stem Cells Into Chondrocytes: Methods and Applications for Disease Modeling and Drug Discovery. Journal of Bone and Mineral Research. 37(3). 397–410. 14 indexed citations

Barallobre‐Barreiro, Javier, Bart Loeys, Manuel Mayr, et al.. (2020). Extracellular Matrix in Vascular Disease, Part 2/4. Journal of the American College of Cardiology. 75(17). 2189–2203. 59 indexed citations

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

10.

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

11.

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

12.

Shukla, Anju, Maaike Alaerts, Dorien Schepers, et al.. (2018). FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature. BMC Medical Genetics. 19(1). 140–140. 19 indexed citations

13.

Alaerts, Maaike, Cuno Kuipéri, Anniek Corveleyn, et al.. (2017). Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation. European Journal of Medical Genetics. 61(1). 8–10. 17 indexed citations

14.

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

15.

Bolar, Nikhita, Aline Verstraeten, Lut Van Laer, & Bart Loeys. (2017). Molecular Insights into Bicuspid Aortic Valve Development and the associated aortopathy. SHILAP Revista de lepidopterología. 4(4). 478–508. 1 indexed citations

16.

Crosiers, David, Aline Verstraeten, Sebastiaan Engelborghs, et al.. (2016). Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson’s disease and increase susceptibility to dementia in a Flanders-Belgian cohort. Neuroscience Letters. 629. 160–164. 20 indexed citations

17.

Bowdin, Sarah, Anne‐Marie Laberge, Aline Verstraeten, & Bart Loeys. (2015). Genetic Testing in Thoracic Aortic Disease—When, Why, and How?. Canadian Journal of Cardiology. 32(1). 131–134. 10 indexed citations

18.

Beek, Gerarda van de, et al.. (2015). TGF-β signalopathies as a paradigm for translational medicine. European Journal of Medical Genetics. 58(12). 695–703. 30 indexed citations

19.

Verstraeten, Aline, David Crosiers, Bram Meeus, et al.. (2012). Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population. Neurobiology of Aging. 33(8). 1844.e11–1844.e13. 16 indexed citations

20.

Meeus, Bram, Aline Verstraeten, Karen Nuytemans, et al.. (2010). Dementia with Lewy Bodies: A Role for Dementia and Parkinson's Disease Genes?. Movement Disorders. 25. 1 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.

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