Bart Loeys

32.3k citations

209 papers · 11.9k indexed · 5 hit papers · h-index 50

Impact in

Genetics top 0.05%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
Pulmonary and Respiratory Medicine top 0.2%
- Aortic Disease and Treatment Approaches
- Aortic aneurysm repair treatments

Papers in ⓘ

Genetics 141
- Connective tissue disorders research 117
Cardiology and Cardiovascular Medicine 72
- Cardiac Valve Diseases and Treatments 28
- Cardiac electrophysiology and arrhythmias 16
- Cardiomyopathy and Myosin Studies 15
- Cardiovascular Issues in Pregnancy 12

Co-authors: Harry C. Dietz (29 shared papers)Daniel P. Judge (7 shared papers)Lut Van Laer (48 shared papers)Jennifer Habashi (6 shared papers)Julie De Backer (17 shared papers)Anne De Paepe (23 shared papers)Bert Callewaert (12 shared papers)Tammy M. Holm (7 shared papers)
Journals: Human Mutation (14 papers)Journal of Medical Genetics (9 papers)European Journal of Human Genetics (7 papers)European Journal of Medical Genetics (7 papers)Stem Cell Research (6 papers)
Partner nations: Belgium Netherlands United States

In The Last Decade

Bart Loeys

200 papers receiving 11.6k citations

Hit Papers

5 papers align trajectories log scale

Loeys–Dietz syndrome: a primer for diagnosis and management 2014 · 338 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2014 Genetics in Medicine
2010 Journal of Medical Genetics
2008 New England Journal of Medicine
2007 Nature Medicine
2006 Science

Peers

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-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.

Border = papers with Bart Loeys Line = papers co-authored together Bart Loeys links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 209 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The revised Ghent nosology for the Marfan syndrome: Table 1 Journal of Medical Genetics ·Bart Loeys, Harry C. Dietz, Alan C. Braverman, Bert Callewaert, Julie De Backer, Richard B. Devereux, Yvonne Hilhorst‐Hofstee, Guillaume Jondeau, Laurence Faivre, Dianna M. Milewicz, Reed E. Pyeritz, Paul D. Sponseller, B P Wordsworth, Anne M. De Paepe Hit paper breakdown →	2010	1350
2	Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome Science ·Jennifer Habashi, Daniel P. Judge, Tammy M. Holm, Ronald D. Cohn, Bart Loeys, Timothy K. Cooper, Loretha Myers, Erin C. Klein, Guosheng Liu, Carla L. Calvi, Megan Podowski, Enid Neptune, Marc K. Halushka, Djahida Bedja, Kathleen Gabrielson, Daniel B. Rifkin, Luca Carta, Francesco Ramirez, David L. Huso, Harry C. Dietz Hit paper breakdown →	2006	1252
3	Angiotensin II Blockade and Aortic-Root Dilation in Marfan's Syndrome New England Journal of Medicine ·Benjamin S. Brooke, Jennifer Habashi, Daniel P. Judge, Nishant Patel, Bart Loeys, Harry C. Dietz Hit paper breakdown →	2008	552
4	Angiotensin II type 1 receptor blockade attenuates TGF-β–induced failure of muscle regeneration in multiple myopathic states Nature Medicine ·Ronald D. Cohn, Christel van Erp, Jennifer Habashi, Arshia Soleimani, Erin C. Klein, Matthew T Lisi, Matthew Gamradt, Colette M ap Rhys, Tammy M. Holm, Bart Loeys, Francesco Ramirez, Daniel P. Judge, Christopher W. Ward, Harry C. Dietz Hit paper breakdown →	2007	542
5	Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation The American Journal of Human Genetics ·Matthew A. Deardorff, Maninder Kaur, Dinah Yaeger, Abhinav Rampuria, Sergey Korolev, Juan Pié, Concepcion Gil-Rodríguez, María Arnedo, Bart Loeys, Antonie D. Kline, Meredith Wilson, K Lillquist, Victoria Mok Siu, Feliciano J. Ramos, Antonio Musio, Laird Jackson, Dale Dorsett, Ian D. Krantz	2007	385
6	Noncanonical TGFβ Signaling Contributes to Aortic Aneurysm Progression in Marfan Syndrome Mice Science ·Tammy M. Holm, Jennifer Habashi, Jefferson J. Doyle, Djahida Bedja, Yi‐Chun Chen, Christel van Erp, Mark E. Lindsay, David Kim, Florian Schoenhoff, Ronald D. Cohn, Bart Loeys, Craig J. Thomas, Samarjit Patnaik, Juan Marugán, Daniel P. Judge, Harry C. Dietz	2011	355
7	Loeys–Dietz syndrome: a primer for diagnosis and management Genetics in Medicine ·Gretchen MacCarrick, James H. Black, Sarah Bowdin, Ismaı̈l El-Hamamsy, Pamela A. Frischmeyer‐Guerrerio, Anthony L. Guerrerio, Paul D. Sponseller, Bart Loeys, Harry C. Dietz Hit paper breakdown →	2014	338
8	The molecular genetics of Marfan syndrome and related disorders Journal of Medical Genetics ·Peter N. Robinson, Emilio Arteaga‐Solis, Clair Baldock, Gwenaëlle Collod‐Béroud, Patrick Booms, Anne De Paepe, Harry C. Dietz, Gao Guo, Penny A Handford, Daniel P. Judge, Cay M. Kielty, Bart Loeys, Dianna M. Milewicz, Andreas Ney, Francesco Ramirez, Dieter P. Reinhardt, Kerstin Tiedemann, Pat Whiteman, Maurice Godfrey	2006	304
9	Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome Nature Genetics ·Paul Coucke, Andy Willaert, Marja W. Wessels, Bert Callewaert, Nicoletta Zoppi, Julie De Backer, Joyce E. Fox, Grazia M.S. Mancini, Marios Kambouris, Rita Gardella, Fabio Facchetti, Patrick J. Willems, Ramses Forsyth, Harry C. Dietz, Sergio Barlati, Marina Colombi, Bart Loeys, Anne De Paepe	2006	246
10	Circulating Transforming Growth Factor-β in Marfan Syndrome Circulation ·Peter Matt, Florian Schoenhoff, Jennifer Habashi, Tammy M. Holm, Christel van Erp, David Loch, Olga D. Carlson, Benjamin F. Griswold, Qin Fu, Julie De Backer, Bart Loeys, David L. Huso, Nazli B. McDonnell, Jennifer E. Van Eyk, Harry C. Dietz	2009	210
11	Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa Human Molecular Genetics ·Bart Loeys	2002	204
12	Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome Annals of Cardiothoracic Surgery ·Josephina Meester, Aline Verstraeten, Dorien Schepers, Maaike Alaerts, Lut Van Laer, Bart Loeys	2017	178
13	Early Surgical Experience With Loeys-Dietz: A New Syndrome of Aggressive Thoracic Aortic Aneurysm Disease The Annals of Thoracic Surgery ·Jason A. Williams, Bart Loeys, Lois U. Nwakanma, Harry C. Dietz, Philip J. Spevak, Nishant Patel, Katrien François, Julie De Backer, Vincent L. Gott, Luca A. Vricella, Duke E. Cameron	2007	171
14	Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome Science Translational Medicine ·Bart Loeys, Elizabeth E. Gerber, Douglas L. Riegert‐Johnson, Sarah Iqbal, Pat Whiteman, Vivienne McConnell, Chandramouli Chillakuri, Daniela Macaya, Paul Coucke, Anne De Paepe, Daniel P. Judge, Fredrick M. Wigley, Elise Davis, Helen J. Mardon, Penny A. Handford, Douglas R. Keene, Lynn Y. Sakai, Harry C. Dietz	2010	165
15	Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Investigative Ophthalmology & Visual Science ·Jill Yardley, Bart P. Leroy, Niki Hart‐Holden, B. A. Lafaut, Bart Loeys, Ludwine Messiaen, Rahat Perveen, M. Ashwin Reddy, Shomi S. Bhattacharya, Elias I. Traboulsi, Diana Baralle, Jean‐Jacques De Laey, Bernard Puech, Philippe Kestelyn, Anthony T. Moore, Forbes Manson, Graeme C. Black	2004	163
16	Genotype and Phenotype Analysis of 171 Patients Referred for Molecular Study of the Fibrillin-1 Gene FBN1 Because of Suspected Marfan Syndrome Archives of Internal Medicine ·Bart Loeys	2001	162
17	Ehlers-Danlos syndromes and Marfan syndrome Best Practice & Research Clinical Rheumatology ·Bert Callewaert, Fransiska Malfait, Bart Loeys, Anne De Paepe	2008	161
18	Loeys-Dietz Syndrome Advances in experimental medicine and biology ·Lut Van Laer, Harry C. Dietz, Bart Loeys	2013	157
19	Recent progress towards a molecular understanding of Marfan syndrome American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Harry C. Dietz, Bart Loeys, Luca Carta, Francesco Ramirez	2005	156
20	Comprehensive molecular screening of theFBN1gene favors locus homogeneity of classical Marfan syndrome Human Mutation ·Bart Loeys, Julie De Backer, Petra Van Acker, K. Wettinck, Gerard Pals, Lieve Nuytinck, Paul Coucke, Anne De Paepe	2004	152

About Bart Loeys

Bart Loeys is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Pulmonary and Respiratory Medicine, Developmental Biology and Genetics, having authored 209 papers that have together received 11.9k indexed citations. Recurring topics across this work include Connective tissue disorders research (117 papers), Aortic Disease and Treatment Approaches (78 papers), Aortic aneurysm repair treatments (48 papers), Cardiac Valve Diseases and Treatments (28 papers), Cardiac electrophysiology and arrhythmias (16 papers), Congenital heart defects research (15 papers), Cardiomyopathy and Myosin Studies (15 papers) and Cardiovascular Issues in Pregnancy (12 papers). The work is most often cited by research in Genetics (7.1k citations), Pulmonary and Respiratory Medicine (5.3k citations), Cardiology and Cardiovascular Medicine (3.3k citations), Cancer Research (955 citations) and Rheumatology (750 citations). Bart Loeys has collaborated with scholars based in Belgium, Netherlands and United States. Frequent 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. Their work appears in journals such as Human Mutation, Journal of Medical Genetics, European Journal of Human Genetics, European Journal of Medical Genetics and Stem Cell Research.

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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