Bart Loeys

32.3k total citations · 5 hit papers
209 papers, 11.9k citations indexed

About

Bart Loeys is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Bart Loeys has authored 209 papers receiving a total of 11.9k indexed citations (citations by other indexed papers that have themselves been cited), including 141 papers in Genetics, 96 papers in Pulmonary and Respiratory Medicine and 72 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Bart Loeys's work include Connective tissue disorders research (117 papers), Aortic Disease and Treatment Approaches (78 papers) and Aortic aneurysm repair treatments (48 papers). Bart Loeys is often cited by papers focused on Connective tissue disorders research (117 papers), Aortic Disease and Treatment Approaches (78 papers) and Aortic aneurysm repair treatments (48 papers). Bart Loeys collaborates with scholars based in Belgium, Netherlands and United States. Bart Loeys's co-authors include Harry C. Dietz, Daniel P. Judge, Lut Van Laer, Jennifer Habashi, Julie De Backer, Anne De Paepe, Bert Callewaert, Tammy M. Holm, Francesco Ramirez and Paul D. Sponseller and has published in prestigious journals such as Science, New England Journal of Medicine and Circulation.

In The Last Decade

Bart Loeys

200 papers receiving 11.6k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The revised Ghent nosology for the Marfan syndrome: Table 1

2010 1.4k citations Bart Loeys, Harry C. Dietz et al. Journal of Medical Genetics profile →
Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome

2006 1.3k citations Bart Loeys, Harry C. Dietz et al. profile →
Angiotensin II Blockade and Aortic-Root Dilation in Marfan's Syndrome

2008 552 citations Nishant Patel, Bart Loeys et al. profile →
Angiotensin II type 1 receptor blockade attenuates TGF-β–induced failure of muscle regeneration in multiple myopathic states

2007 542 citations Bart Loeys, Harry C. Dietz et al. profile →
Loeys–Dietz syndrome: a primer for diagnosis and management

2014 338 citations Bart Loeys, Harry C. Dietz et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Bart Loeys Belgium	50	7.1k	5.3k	3.3k	3.0k	1.8k	209	11.9k
Daniel P. Judge United States	66	4.6k 0.7×	3.6k 0.7×	8.9k 2.7×	4.8k 1.6×	1.8k 1.0×	220	16.1k
Clair A. Francomano United States	54	6.2k 0.9×	1.7k 0.3×	1.2k 0.4×	4.2k 1.4×	1.7k 0.9×	168	11.0k
Hiromi Yanagisawa United States	43	2.2k 0.3×	1.3k 0.2×	840 0.3×	3.3k 1.1×	1.1k 0.6×	112	7.0k
Craig T. Basson United States	41	1.3k 0.2×	1.4k 0.3×	2.7k 0.8×	4.4k 1.5×	1.5k 0.9×	87	7.9k
Dean Y. Li United States	51	1.1k 0.2×	1.2k 0.2×	1.2k 0.4×	4.1k 1.4×	1.9k 1.1×	119	9.9k
Maria G. Frid United States	44	662 0.1×	3.6k 0.7×	1.3k 0.4×	3.0k 1.0×	1.1k 0.6×	79	7.6k
Marco C. DeRuiter Netherlands	50	880 0.1×	1.5k 0.3×	1.4k 0.4×	3.3k 1.1×	2.0k 1.1×	177	6.8k
Mark W. Majesky United States	48	824 0.1×	1.2k 0.2×	1.5k 0.4×	5.4k 1.8×	2.4k 1.4×	100	10.0k
Beat Steinmann Switzerland	45	3.3k 0.5×	734 0.1×	517 0.2×	2.1k 0.7×	864 0.5×	123	6.4k
Volkhard Lindner United States	50	890 0.1×	999 0.2×	1.2k 0.4×	4.7k 1.6×	1.6k 0.9×	90	9.1k

Countries citing papers authored by Bart Loeys

Since Specialization

Citations

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

Fields of papers citing papers by Bart Loeys

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bart Loeys

This figure shows the co-authorship network connecting the top 25 collaborators of Bart Loeys. A scholar is included among the top collaborators of Bart Loeys 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 Bart Loeys. Bart Loeys 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

Vandendriessche, Benjamin, et al.. (2024). Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin. Stem Cell Research. 81. 103536–103536. 1 indexed citations

Adlam, David, Fleur S van Dijk, & Bart Loeys. (2024). Genetic testing in patients with unexplained coronary aneurysms or dilation. European Heart Journal. 45(18). 1610–1612. 1 indexed citations

Alaerts, Maaike, Lut Van Laer, Johan Saenen, et al.. (2024). Phenotypic spectrum of the first Belgian MYBPC3 founder: a large multi-exon deletion with a varying phenotype. Frontiers in Genetics. 15. 1392527–1392527. 2 indexed citations

Totten, Vicken Y., Gisela Teixidó‐Turà, Paula Fernández‐Álvarez, et al.. (2024). Arterial aneurysm and dissection: toward the evolving phenotype of Tatton-Brown-Rahman syndrome. Journal of Medical Genetics. 61(9). 870–877. 1 indexed citations

Loeys, Bart, et al.. (2023). iPSC-Derived Cardiomyocytes in Inherited Cardiac Arrhythmias: Pathomechanistic Discovery and Drug Development. Biomedicines. 11(2). 334–334. 7 indexed citations

Vandendriessche, Benjamin, Charlotte Claes, Maaike Alaerts, et al.. (2023). Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping. Scientific Reports. 13(1). 1491–1491. 5 indexed citations

Hendriks, Jeroen, et al.. (2022). Retrograde Type A Aortic Dissection 48 Hours after TEVAR in a Patient with a Delayed Diagnosis of Vascular Ehlers-Danlos Syndrome. Aorta. 10(3). 141–144. 1 indexed citations

Castelletti, Silvia, Belinda Gray, Cristina Basso, et al.. (2022). Indications and utility of cardiac genetic testing in athletes. European Journal of Preventive Cardiology. 29(12). 1582–1591. 18 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

10.

Pals, Gerard, Aeilko H. Zwinderman, Marieke J.H. Baars, et al.. (2022). Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships. American Journal of Medical Genetics Part A. 191(2). 479–489. 3 indexed citations

11.

Laar, Ingrid M.B.H. van de, Annette F. Baas, Julie De Backer, et al.. (2022). Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN). European Journal of Medical Genetics. 65(9). 104557–104557. 8 indexed citations

12.

Kumar, Ajay, Bart Loeys, Gerarda van de Beek, et al.. (2022). varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data. Bioinformatics. 39(1). 2 indexed citations

13.

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

14.

Kopljar, Ivan, Maaike Alaerts, Ard Teisman, et al.. (2021). The resting membrane potential of hSC-CM in a syncytium is more hyperpolarised than that of isolated cells. Channels. 15(1). 239–252. 14 indexed citations

15.

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

16.

Verhagen, Judith M.A., Marlies Kempers, Luc Cozijnsen, et al.. (2018). Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives. International Journal of Cardiology. 258. 243–248. 40 indexed citations

17.

Hoven, Allard T. van den, Raluca G. Chelu, Anthonie L. Duijnhouwer, et al.. (2017). Partial anomalous pulmonary venous return in Turner syndrome. European Journal of Radiology. 95. 141–146. 16 indexed citations

18.

Bolar, Nikhita, Arnaud Vanlander, Nathalie Van der Aa, et al.. (2013). Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy. Human Molecular Genetics. 22(13). 2590–2602. 90 indexed citations

19.

Williams, Jason A., Bart Loeys, Lois U. Nwakanma, et al.. (2007). Early Surgical Experience With Loeys-Dietz: A New Syndrome of Aggressive Thoracic Aortic Aneurysm Disease. The Annals of Thoracic Surgery. 83(2). S757–S763. 171 indexed citations

20.

Leroy, Bart P., Niki Hart‐Holden, B. A. Lafaut, et al.. (2004). Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC). Investigative Ophthalmology & Visual Science. 45(10). 3683–3683. 163 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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