Josephina Meester

1.6k total citations
24 papers, 479 citations indexed

About

Josephina Meester is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Josephina Meester has authored 24 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 15 papers in Pulmonary and Respiratory Medicine and 7 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Josephina Meester's work include Connective tissue disorders research (18 papers), Aortic Disease and Treatment Approaches (13 papers) and Aortic aneurysm repair treatments (6 papers). Josephina Meester is often cited by papers focused on Connective tissue disorders research (18 papers), Aortic Disease and Treatment Approaches (13 papers) and Aortic aneurysm repair treatments (6 papers). Josephina Meester collaborates with scholars based in Belgium, Netherlands and United States. Josephina Meester's co-authors include Bart Loeys, Aline Verstraeten, Lut Van Laer, Maaike Alaerts, Dorien Schepers, Geert Mortier, Wim Wuyts, Marlies Kempers, Vardit Kram and Priyam Jani and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Journal of Bone and Mineral Research.

In The Last Decade

Josephina Meester

24 papers receiving 469 citations

Peers

Josephina Meester
Fleur S van Dijk Netherlands
Van Tran‐Fadulu United States
Vishwanathan Hucthagowder United States
Anne‐Laure Fauret France
Shelby L. Chapman United States
Somyoth Sridurongrit United States
Leema Robert United Kingdom
James J. Earley United States
Valeria Bozzi Italy
Kimberly Sauls United States
Fleur S van Dijk Netherlands
Josephina Meester
Citations per year, relative to Josephina Meester Josephina Meester (= 1×) peers Fleur S van Dijk

Countries citing papers authored by Josephina Meester

Since Specialization
Citations

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

Fields of papers citing papers by Josephina Meester

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josephina Meester

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

All Works

20 of 20 papers shown
1.
Meester, Josephina, et al.. (2024). An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome. Drug Discovery Today. 29(7). 104023–104023. 3 indexed citations
2.
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
3.
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
4.
Meester, Josephina, et al.. (2023). Structural genomic variants in thoracic aortic disease. Current Opinion in Cardiology. 38(3). 157–161. 3 indexed citations
5.
6.
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
7.
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
8.
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
9.
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.
Meester, Josephina, et al.. (2021). Meester-Loeys Syndrome. Advances in experimental medicine and biology. 1348. 265–272. 6 indexed citations
11.
Nayak, Shalini S., Siddaramappa J. Patil, Neethukrishna Kausthubham, et al.. (2021). Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing. Scientific Reports. 11(1). 764–764. 9 indexed citations
12.
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
13.
Kram, Vardit, et al.. (2020). Biglycan in the Skeleton. Journal of Histochemistry & Cytochemistry. 68(11). 747–762. 33 indexed citations
14.
Verstraeten, Aline, et al.. (2020). Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular Intersection. Trends in Molecular Medicine. 26(8). 783–795. 5 indexed citations
15.
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
16.
Schroder, Kim, Duygu Duman, Mustafa Tekin, et al.. (2019). Adams–Oliver syndrome caused by mutations of the EOGT gene. American Journal of Medical Genetics Part A. 179(11). 2246–2251. 16 indexed citations
17.
Meester, Josephina, Aline Verstraeten, Maaike Alaerts, et al.. (2018). Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease. Clinical Genetics. 95(1). 85–94. 45 indexed citations
18.
Meester, Josephina, Aline Verstraeten, Dorien Schepers, et al.. (2017). Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome. ASVIDE. 4. 544–544. 6 indexed citations
19.
Meester, Josephina, Aline Verstraeten, Dorien Schepers, et al.. (2017). Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome. Annals of Cardiothoracic Surgery. 6(6). 582–594. 178 indexed citations
20.
Fedorenko, Victor, et al.. (2016). Identification of FBN1 gene mutations in Ukrainian Marfan syndrome patients. Genetics Research. 98. e13–e13. 3 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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