Bart P. Leroy

13.5k total citations · 1 hit paper
157 papers, 4.8k citations indexed

About

Bart P. Leroy is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Bart P. Leroy has authored 157 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 104 papers in Molecular Biology, 69 papers in Ophthalmology and 46 papers in Genetics. Recurrent topics in Bart P. Leroy's work include Retinal Development and Disorders (84 papers), Retinal Diseases and Treatments (48 papers) and Connexins and lens biology (14 papers). Bart P. Leroy is often cited by papers focused on Retinal Development and Disorders (84 papers), Retinal Diseases and Treatments (48 papers) and Connexins and lens biology (14 papers). Bart P. Leroy collaborates with scholars based in Belgium, United States and United Kingdom. Bart P. Leroy's co-authors include Elfride De Baere, Frauke Coppieters, Albert M. Maguire, Carel B. Hoyng, Anneke I. den Hollander, Jean Bennett, Julie De Zaeytijd, Steve Lefever, Paul Coucke and Camiel J.F. Boon and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Annals of Internal Medicine.

In The Last Decade

Bart P. Leroy

147 papers receiving 4.7k citations

Hit 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.

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

2019 276 citations Albert M. Maguire, Daniel C. Chung 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 P. Leroy Belgium	37	3.6k	2.0k	1.5k	661	579	157	4.8k
Patrick Calvas France	31	2.1k 0.6×	915 0.5×	1.4k 1.0×	348 0.5×	721 1.2×	104	3.9k
Elise Héon Canada	44	5.1k 1.4×	3.9k 2.0×	1.7k 1.1×	833 1.3×	1.5k 2.7×	144	7.3k
Alan D. Marmorstein United States	42	4.2k 1.2×	1.8k 0.9×	473 0.3×	1.0k 1.5×	555 1.0×	99	5.4k
Alison J. Hardcastle United Kingdom	39	3.0k 0.8×	1.6k 0.8×	763 0.5×	541 0.8×	1.1k 1.9×	127	4.2k
Norman L. Hawes United States	26	3.5k 1.0×	2.0k 1.0×	694 0.5×	482 0.7×	495 0.9×	46	4.3k
G. Jane Farrar Ireland	35	3.5k 1.0×	1.1k 0.6×	709 0.5×	434 0.7×	369 0.6×	93	4.1k
Paul F. Kenna Ireland	38	3.9k 1.1×	1.4k 0.7×	666 0.4×	595 0.9×	504 0.9×	121	4.8k
Elizabeth C. Engle United States	39	1.9k 0.5×	407 0.2×	1.2k 0.8×	799 1.2×	259 0.4×	112	4.4k
Isabelle Audo France	32	3.1k 0.9×	2.1k 1.1×	465 0.3×	327 0.5×	601 1.0×	184	4.0k
Amir Rattner United States	33	4.1k 1.1×	650 0.3×	645 0.4×	607 0.9×	246 0.4×	62	5.3k

Countries citing papers authored by Bart P. Leroy

Since Specialization

Citations

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

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-authorship network of co-authors of Bart P. Leroy

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

Boon, Camiel J. F., Martijn C.G.J. Brouwers, Roselie M.H. Diederen, et al.. (2025). Novel Insights Into Gyrate Atrophy of the Choroid and Retina (GACR): A Cohort Study. Journal of Inherited Metabolic Disease. 48(1). e12842–e12842. 1 indexed citations

Saletti, Veronica, Agnese Suppiej, Hélène Dollfus, et al.. (2024). Quality of life, functioning and participation of children and adolescents with visual impairment: A scoping review. Research in Developmental Disabilities. 151. 104772–104772. 4 indexed citations

Postelmans, Laurence, Laure Caspers, Francis Corazza, et al.. (2024). DIAGNOSTIC YIELD OF AN INHERITED RETINAL DISEASE GENE PANEL IN RETINOPATHY OF UNKNOWN ORIGIN. Retina. 44(9). 1597–1607.

Schooneveld, Mary J. van, Roselie M.H. Diederen, Jacoline B. ten Brink, et al.. (2023). Efficacy of Carbonic Anhydrase Inhibitors on Cystoid Fluid Collections and Visual Acuity in Patients with X-Linked Retinoschisis. Ophthalmology Retina. 8(6). 600–606. 5 indexed citations

Fischer, Suzanne, Laurence Campens, Andreas Pasch, et al.. (2022). Serum Calcification Propensity T50 Associates with Disease Severity in Patients with Pseudoxanthoma Elasticum. Journal of Clinical Medicine. 11(13). 3727–3727. 7 indexed citations

Thiadens, Alberta A. H. J., Marta Fiocco, Martin McKibbin, et al.. (2022). Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa. American Journal of Ophthalmology. 246. 1–9. 11 indexed citations

Georgiou, Michalis, Mary J. van Schooneveld, Elfride De Baere, et al.. (2021). The Phenotypic Spectrum of Patients with PHARC Syndrome Due to Variants in ABHD12: An Ophthalmic Perspective. Genes. 12(9). 1404–1404. 12 indexed citations

Ueno, Shinji, Taro Chaya, Shunsuke Yasuda, et al.. (2021). Broad locations of antigenic regions for anti-TRPM1 autoantibodies in paraneoplastic retinopathy with retinal ON bipolar cell dysfunction. Experimental Eye Research. 212. 108770–108770. 5 indexed citations

Hosen, Mohammad Jakir, Ludovic Martin, Julie De Zaeytijd, et al.. (2020). VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticum. Clinical Genetics. 98(1). 74–79. 9 indexed citations

10.

Schil, Kristof Van, Caroline Van Cauwenbergh, Toon Rosseel, et al.. (2019). Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease (IRD) expands the molecular and phenotypic spectrum of recently identified IRD genes. Ghent University Academic Bibliography (Ghent University). 1 indexed citations

11.

Naessens, Sarah, Julie De Zaeytijd, Delfien Syx, et al.. (2019). The N‐terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond. Human Mutation. 40(5). 539–551. 10 indexed citations

12.

Talib, Mays, Mary J. van Schooneveld, Caroline Van Cauwenbergh, et al.. (2018). The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in theRPGRGene. Investigative Ophthalmology & Visual Science. 59(10). 4123–4123. 44 indexed citations

13.

Bogaert, Debby, Mélissa Dullaers, Hye Sun Kuehn, et al.. (2017). Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes. Scientific Reports. 7(1). 3702–3702. 22 indexed citations

14.

Lee, Helena, Ravi Purohit, Viral Sheth, et al.. (2015). Retinal Development in Achromatopsia: A Prospective Study of Infants and Young Children using Optical Coherence Tomography. Investigative Ophthalmology & Visual Science. 56(7). 5855–5855. 1 indexed citations

15.

Thomas, Mervyn G., Moira Crosier, Susan Lindsay, et al.. (2012). Retinal Changes In Idiopathic Infantile Nystagmus Associated With FRMD7 Mutations. Investigative Ophthalmology & Visual Science. 53(14). 520–520. 1 indexed citations

16.

Ashtari, Manzar, Laura Cyckowski, Justin F. Monroe, et al.. (2011). The human visual cortex responds to gene therapy–mediated recovery of retinal function. Journal of Clinical Investigation. 121(6). 2160–2168. 107 indexed citations

17.

Sergouniotis, Panagiotis I., Donna S. Mackay, Alexander Day, et al.. (2010). A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy.. PubMed. 16. 540–8. 33 indexed citations

18.

Audo, Isabelle, Olivier Vanakker, Bart P. Leroy, et al.. (2007). Pseudoxanthoma Elasticum with Generalized Retinal Dysfunction, a Common Finding?. Investigative Ophthalmology & Visual Science. 48(9). 4250–4250. 21 indexed citations

19.

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

20.

Bhattacharya, Siladitya, Ronak Patel, Leen Abu‐Safieh, et al.. (2003). Evaluation of the Retbindin Gene as a Candidate for Retinal Diseases. Investigative Ophthalmology & Visual Science. 44(13). 2322–2322. 1 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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