Bart P. Leroy

13.5k citations

157 papers · 4.8k · 1 hit paper · h-index 37

Impact in

Ophthalmology top 0.2%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
- Retinal and Optic Conditions
Genetics top 1%
- Dermatological and Skeletal Disorders
- Ocular Disorders and Treatments

Papers in

Molecular Biology 104
- Retinal Development and Disorders 84
- Connexins and lens biology 14
Ophthalmology 69
- Retinal Diseases and Treatments 48
- Glaucoma and retinal disorders 11

Co-authors: Elfride De Baere (50 shared papers)Frauke Coppieters (23 shared papers)Albert M. Maguire (9 shared papers)Carel B. Hoyng (10 shared papers)Anneke I. den Hollander (5 shared papers)Jean Bennett (8 shared papers)Julie De Zaeytijd (34 shared papers)Paul Coucke (14 shared papers)
Journals: Investigative Ophthalmology & Visual Science (15 papers)Ophthalmic Genetics (7 papers)Human Mutation (7 papers)Retina (7 papers)Scientific Reports (6 papers)
Partner nations: Belgium United States United Kingdom

In The Last Decade

Bart P. Leroy

147 papers receiving 4.7k citations

Hit Papers

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Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation–Associated Inherited Retinal Dystrophy 2019 · 276 citations

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Countries citing papers authored by Bart P. Leroy

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Citations

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Fields of papers citing papers by Bart P. Leroy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Bart P. Leroy, 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 P. Leroy Line = papers co-authored together Bart P. Leroy 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 157 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation–Associated Inherited Retinal Dystrophy Ophthalmology ·Albert M. Maguire, Stephen R. Russell, Jennifer Wellman, Daniel C. Chung, Zi‐Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan U. Elci, Kathleen Marshall, Sarah McCague, Hannah Reichert, Maria Davis, Francesca Simonelli, Bart P. Leroy, J. Fraser Wright, Katherine A. High, Jean Bennett Hit paper breakdown →	2019	276
2	The spectrum of ocular phenotypes caused by mutations in the BEST1 gene Progress in Retinal and Eye Research ·Camiel J.F. Boon, B. Jeroen Klevering, Bart P. Leroy, Carel B. Hoyng, Jan E.E. Keunen, Anneke I. den Hollander	2009	253
3	Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans The American Journal of Human Genetics ·Rosemary Burgess, I. D. Millar, Bart P. Leroy, Jill Urquhart, Ian M. Fearon, Elfrida De Baere, Peter de Nully Brown, Anthony G. Robson, Genevieve Wright, Philippe Kestelyn, Graham E. Holder, Andrew R. Webster, Forbes Manson, Graeme C. Black	2008	225
4	CEP290, a gene with many faces: mutation overview and presentation of CEP290base Human Mutation ·Frauke Coppieters, Steve Lefever, Bart P. Leroy, Elfride De Baere	2010	210
5	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
6	Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders The American Journal of Human Genetics ·Alberta A. H. J. Thiadens, Anneke I. den Hollander, Susanne Roosing, Sander B. Nabuurs, Renate C. Zekveld-Vroon, Rob W.J. Collin, Elfride De Baere, Robert K. Koenekoop, Mary J. van Schooneveld, Tim M. Strom, Janneke J.C. van Lith-Verhoeven, Andrew Lotery, Norka van Moll-Ramirez, Bart P. Leroy, L. Ingeborgh van den Born, Carel B. Hoyng, Frans P.M. Cremers, Caroline C. W. Klaver	2009	159
7	Pseudoxanthoma Elasticum-Like Phenotype with Cutis Laxa and Multiple Coagulation Factor Deficiency Represents a Separate Genetic Entity Journal of Investigative Dermatology ·Olivier Vanakker, Ludovic Martin, Dealba Gheduzzi, Bart P. Leroy, Bart Loeys, Veronica Ileana Guerci, Dirk Matthys, Sharon F. Terry, Paul Coucke, I. Pasquali‐Ronchetti, Anne De Paepe	2006	139
8	Prevalence of AIPL1 Mutations in Inherited Retinal Degenerative Disease Molecular Genetics and Metabolism ·Melanie M. Sohocki, Isabelle Perrault, Bart P. Leroy, Annette Payne, Sharola Dharmaraj, Shomi S. Bhattacharya, Josseline Kaplan, Irene H. Maumenee, Robert K. Koenekoop, Françoise Meire, David G. Birch, John R. Heckenlively, Stephen P. Daiger	2000	129
9	Chromosomal Duplication Involving the Forkhead Transcription Factor Gene FOXC1 Causes Iris Hypoplasia and Glaucoma The American Journal of Human Genetics ·Ordan J. Lehmann, Neil D. Ebenezer, Tim Jordan, Margaret Fox, Louise Ocaka, Annette Payne, Bart P. Leroy, Brian J. Clark, Roger A. Hitchings, Sue Povey, Peng T. Khaw, Shomi S. Bhattacharya	2000	129
10	Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease Ophthalmology ·Albert M. Maguire, Stephen R. Russell, Daniel C. Chung, Zi‐Fan Yu, Amy Tillman, Arlene V. Drack, Francesca Simonelli, Bart P. Leroy, Kathleen Z. Reape, Katherine A. High, Jean Bennett	2021	124
11	Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes Human Mutation ·Frauke Coppieters, Ingele Casteels, Françoise Meire, Sarah De Jaegere, Sally Hooghe, Nicole Van Regemorter, Hilde Van Esch, Aušra Matulevičienė, Luís Nunes, Valérie Meersschaut, Sophie Walraedt, Lieve Standaert, Paul Coucke, Heidi Hoeben, Hester Y. Kroes, Johan Vande Walle, Thomy de Ravel, Bart P. Leroy, Elfride De Baere	2010	110
12	Clinical Perspective: Treating RPE65-Associated Retinal Dystrophy Molecular Therapy ·Albert M. Maguire, Jean Bennett, Elena M. Aleman, Bart P. Leroy, Tomás S. Alemán	2020	109
13	The human visual cortex responds to gene therapy–mediated recovery of retinal function Journal of Clinical Investigation ·Manzar Ashtari, Laura Cyckowski, Justin F. Monroe, Kathleen Marshall, Daniel C. Chung, Alberto Auricchio, Francesca Simonelli, Bart P. Leroy, Albert M. Maguire, Kenneth S. Shindler, Jean Bennett	2011	107
14	An update on the ocular phenotype in patients with pseudoxanthoma elasticum Frontiers in Genetics ·Martin Gliem, Julie De Zaeytijd, Robert P. Finger, Frank G. Holz, Bart P. Leroy, Peter Charbel Issa	2013	98
15	Recurrent Mutation in the First Zinc Finger of the Orphan Nuclear Receptor NR2E3 Causes Autosomal Dominant Retinitis Pigmentosa The American Journal of Human Genetics ·Frauke Coppieters, Bart P. Leroy, Diane Beysen, Jan Hellemans, Karolien De Bosscher, Guy Haegeman, Kirsten Robberecht, Wim Wuyts, Paul Coucke, Elfride De Baere	2007	96
16	Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone–Rod Dystrophy Ophthalmology ·Alberta A. H. J. Thiadens, T. My Lan Phan, Renate C. Zekveld-Vroon, Bart P. Leroy, L. Ingeborgh van den Born, Carel B. Hoyng, Caroline C. W. Klaver, Susanne Roosing, Jan-Willem R. Pott, Mary J. van Schooneveld, Norka van Moll-Ramirez, Maria M. van Genderen, Camiel J.F. Boon, Anneke I. den Hollander, Arthur A. Bergen, Elfride De Baere, Frans P.M. Cremers, Andrew Lotery	2012	93
17	Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis Investigative Ophthalmology & Visual Science ·Suzanne Yzer, Bart P. Leroy, Elfride De Baere, Thomy de Ravel, Marijke N. Zonneveld, Krysta Voesenek, Ulrich Kellner, José P. Martinez Ciriano, Jan-Tjeerd H.N. de Faber, Klaus Rohrschneider, Ronald Roepman, Anneke I. den Hollander, J.R.M. Cruysberg, Franc ̧oise Meire, Ingele Casteels, Norka G. van Moll-Ramirez, Rando Allikmets, L. Ingeborgh van den Born, Frans P.M. Cremers	2006	77
18	Novel clinico-molecular insights in pseudoxanthoma elasticum provide an efficient molecular screening method and a comprehensive diagnostic flowchart Human Mutation ·Olivier Vanakker, Bart P. Leroy, Paul Coucke, Lionel Bercovitch, Jouni Uitto, Dennis Viljoen, Sharon F. Terry, Petra Van Acker, Dirk Matthys, Bart Loeys, Anne De Paepe	2007	72
19	Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa Ophthalmology ·Laurence Pierrache, Bas P. Hartel, Erwin van Wijk, Magda A. Meester‐Smoor, Frans P.M. Cremers, Elfride De Baere, Julie De Zaeytijd, Mary J. van Schooneveld, Cor W. R. J. Cremers, Gislin Dagnelie, Carel B. Hoyng, Arthur A. Bergen, Bart P. Leroy, Ronald J. E. Pennings, L. Ingeborgh van den Born, Caroline C. W. Klaver	2016	67
20	Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation Human Molecular Genetics ·Diane Beysen, Lara Moumné, Reiner A. Veitia, Hartmut Peters, Bart P. Leroy, Anne De Paepe, Elfride De Baere	2008	66

About Bart P. Leroy

Bart P. Leroy is a scholar working on Molecular Biology, Ophthalmology, Genetics, Radiology, Nuclear Medicine and Imaging and Cell Biology, having authored 157 papers that have together received 4.8k indexed citations. Recurring topics across this work include Retinal Development and Disorders (84 papers), Retinal Diseases and Treatments (48 papers), Connexins and lens biology (14 papers), Ocular Disorders and Treatments (13 papers), Dermatological and Skeletal Disorders (12 papers), Glaucoma and retinal disorders (11 papers), Retinopathy of Prematurity Studies (11 papers) and Skin and Cellular Biology Research (10 papers). The work is most often cited by research in Ophthalmology (2.0k citations), Genetics (1.5k citations), Molecular Biology (3.6k citations), Cell Biology (661 citations) and Sensory Systems (179 citations). Bart P. Leroy has collaborated with scholars based in Belgium, United States and United Kingdom. Frequent co-authors include Elfride De Baere, Frauke Coppieters, Albert M. Maguire, Carel B. Hoyng, Anneke I. den Hollander, Jean Bennett, Julie De Zaeytijd, Paul Coucke, Steve Lefever and Camiel J.F. Boon. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Ophthalmic Genetics, Human Mutation, Retina and Scientific Reports.

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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