Bart P. Leroy

13.8k citations

160 papers · 5.1k · h-index 38

Impact in

Ophthalmology top 0.2%
- Retinal Diseases and Treatments
- Retinal and Optic Conditions
Genetics top 1%
- Dermatological and Skeletal Disorders
- Ocular Disorders and Treatments
- Genetic and Kidney Cyst Diseases

Papers in

Molecular Biology 85
- Retinal Development and Disorders 71
- Connexins and lens biology 7
- RNA regulation and disease 6
Genetics 40
- Dermatological and Skeletal Disorders 12
- Ocular Disorders and Treatments 10
- Connective tissue disorders research 7

Co-authors: Frauke Coppieters (24 shared papers)Albert M. Maguire (9 shared papers)Carel B. Hoyng (10 shared papers)Jean Bennett (8 shared papers)Anneke I. den Hollander (5 shared papers)Julie De Zaeytijd (35 shared papers)Paul Coucke (14 shared papers)Steve Lefever (3 shared papers)
Journals: Investigative Ophthalmology & Visual Science (15 papers)Ophthalmic Genetics (7 papers)Human Mutation (7 papers)Retina (7 papers)The American Journal of Human Genetics (7 papers)
Partner nations: Belgium United States United Kingdom

In The Last Decade

Bart P. Leroy

149 papers receiving 5.0k citations

Peers

Countries citing papers authored by Bart P. Leroy

Since Specialization

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 160 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	2019	290
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	256
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	228
4	CEP290, a gene with many faces: mutation overview and presentation of CEP290base Human Mutation ·Frauke Coppieters, Steve Lefever, Bart P. Leroy, (unknown)	2010	214
5	FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation The American Journal of Human Genetics ·(unknown), Diane Beysen, Christine Oley, Birgit Lorenz, Julie Cocquet, Paul De Sutter, Koenraad Devriendt, Michael J. Dixon, Marc Fellous, Jean‐Pierre Fryns, Arturo Garza, Christoffer Jonsrud, Pasi A. Koivisto, Amanda Krause, Bart P. Leroy, Françoise Meire, Astrid S. Plomp, Lionel Van Maldergem, Anne De Paepe, Reiner A. Veitia, Ludwine Messiaen	2003	187
6	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	164
7	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, (unknown), 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	160
8	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	140
9	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	134
10	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	130
11	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	128
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	116
13	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, (unknown)	2010	111
14	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	108
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, (unknown)	2007	100
16	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	99
17	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, (unknown), Frans P.M. Cremers, Andrew Lotery	2012	94
18	Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis Investigative Ophthalmology & Visual Science ·Suzanne Yzer, Bart P. Leroy, (unknown), 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	78
19	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	73
20	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, (unknown), 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

About Bart P. Leroy

Bart P. Leroy is a scholar working on Molecular Biology, Genetics, Ophthalmology, Cell Biology and Radiology, Nuclear Medicine and Imaging, having authored 160 papers that have together received 5.1k indexed citations. Recurring topics across this work include Retinal Development and Disorders (71 papers), Retinal Diseases and Treatments (26 papers), Dermatological and Skeletal Disorders (12 papers), Ocular Disorders and Treatments (10 papers), Connexins and lens biology (7 papers), Connective tissue disorders research (7 papers), Skin and Cellular Biology Research (7 papers) and RNA regulation and disease (6 papers). The work is most often cited by research in Ophthalmology (1.2k citations), Genetics (1.4k citations), Molecular Biology (3.3k citations), Sensory Systems (162 citations) and Cell Biology (480 citations). Bart P. Leroy has collaborated with scholars based in Belgium, United States and United Kingdom. Frequent co-authors include Frauke Coppieters, Albert M. Maguire, Carel B. Hoyng, Jean Bennett, Anneke I. den Hollander, Julie De Zaeytijd, Paul Coucke, Steve Lefever, Camiel J.F. Boon and Shomi S. Bhattacharya. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Ophthalmic Genetics, Human Mutation, Retina and The American Journal of Human Genetics.

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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