Bart Loeys
Impact in
- Genetics top 0.05%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Cardiomyopathy and Myosin Studies
Papers in
- Genetics 235
- Connective tissue disorders research 179
- Genomics and Rare Diseases 30
- Genomic variations and chromosomal abnormalities 16
- Genetics and Neurodevelopmental Disorders 8
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- Cardiac electrophysiology and arrhythmias 21
- Cardiomyopathy and Myosin Studies 14
- Co-authors
- Harry C. Dietz (34 shared papers)Lut Van Laer (51 shared papers)Daniel Philip Judge (7 shared papers)Jennifer Pardo Habashi (6 shared papers)Julie F A De Backer (20 shared papers)Anne De Paepe (25 shared papers)Bert Louis Callewaert (13 shared papers)Tammy M. Holm (7 shared papers)
- Journals
- Human Mutation (21 papers)European Journal of Human Genetics (14 papers)Journal of Medical Genetics (14 papers)European Journal of Medical Genetics (12 papers)Genetics in Medicine (12 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Bart Loeys
313 papers receiving 25.9k citations
Bart Loeys's Hit Papers
Peers
Comparison fields: 5 of 148
- Genetics 14.5k
- Cardiology and Cardiovascular Medicine 3.5k
- Pulmonary and Respiratory Medicine 4k
- Developmental Biology 142
- Infectious Diseases 1.1k
Countries citing papers authored by Bart Loeys
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
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-authors
The 25 scholars most cited alongside Bart Loeys, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 322 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 Hit paper breakdown → | 2020 | 1757 |
| 2 | The revised Ghent nosology for the Marfan syndrome: Table 1 Hit paper breakdown → | 2010 | 1572 |
| 3 | 2023 ESC Guidelines for the management of cardiomyopathies Hit paper breakdown → | 2023 | 1503 |
| 4 | Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome Hit paper breakdown → | 2006 | 1440 |
| 5 | A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 Hit paper breakdown → | 2005 | 1400 |
| 6 | Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor Hit paper breakdown → | 2006 | 1274 |
| 7 | Angiotensin II Blockade and Aortic-Root Dilation in Marfan's Syndrome Hit paper breakdown → | 2008 | 651 |
| 8 | 2007 | 576 | |
| 9 | 2007 | 450 | |
| 10 | 2007 | 433 | |
| 11 | Loeys–Dietz syndrome: a primer for diagnosis and management Hit paper breakdown → | 2014 | 408 |
| 12 | Atenolol versus Losartan in Children and Young Adults with Marfan's Syndrome Hit paper breakdown → | 2014 | 396 |
| 13 | 2011 | 389 | |
| 14 | 2012 | 383 | |
| 15 | 2006 | 340 | |
| 16 | 2005 | 339 | |
| 17 | 2006 | 302 | |
| 18 | 2003 | 274 | |
| 19 | 2009 | 261 | |
| 20 | 2015 | 241 |
About Bart Loeys
Bart Loeys is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Pulmonary and Respiratory Medicine, Molecular Biology and Developmental Biology, having authored 322 papers that have together received 27k indexed citations. Recurring topics across this work include Connective tissue disorders research (179 papers), Genomics and Rare Diseases (30 papers), Aortic Disease and Treatment Approaches (27 papers), Cardiac electrophysiology and arrhythmias (21 papers), Genomic variations and chromosomal abnormalities (16 papers), Cardiomyopathy and Myosin Studies (14 papers), Pluripotent Stem Cells Research (11 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (14.5k citations), Cardiology and Cardiovascular Medicine (3.5k citations), Pulmonary and Respiratory Medicine (4k citations), Developmental Biology (142 citations) and Infectious Diseases (1.1k citations). Bart Loeys has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Harry C. Dietz, Lut Van Laer, Daniel Philip Judge, Jennifer Pardo Habashi, Julie F A De Backer, Anne De Paepe, Bert Louis Callewaert, Tammy M. Holm, Francesco Ramirez and Aline Verstraeten. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Journal of Medical Genetics, European Journal of Medical Genetics and Genetics in Medicine.
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.