Bart Leroy

基本信息

Career Trajectory

Bio

Dr. Leroy’s focus is diagnosis and detailed clinical phenotyping of inherited retinal degenerations as well as in the development of innovative treatments, including serving as a clinical investigator on therapies for RPE65-IRD and CEP290-IRD. He served as past president for the European Organization for Vision & Eye Research and is a board member of the International Society for Genetic Eye Disease & Retinoblastoma, the Société de la Génétique Ophtalmologique Francophone, and the Belgian Society of Ophthalmology. He is also co-opted board member for ophthalmic genetics of the European Society of Retina Specialists (EURETINA).

Research Interests

Papers共 403 篇Author StatisticsCo-AuthorSimilar Experts

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Bi-allelic Variants in Three Genes Encoding Distinct Subunits of the Vesicular AP-5 Complex Cause Hereditary Macular Dystrophy

Karolina Kaminska, Francesca Cancellieri, Mathieu Quinodoz, Abigail R Moye, Miriam Bauwens,Siying Lin, Lucas Janeschitz-Kriegl, Tamar Hayman, Pilar Barberán-Martínez,Regina Schlaeger, Filip Van den Broeck,Almudena Ávila Fernández, Lidia Fernández-Caballero, Irene Perea-Romero,Gema García-García,David Salom, Pascale Mazzola, Theresia Zuleger, Karin Poths,Tobias B Haack,Julie Jacob,Sascha Vermeer, Frédérique Terbeek, Nicolas Feltgen, Alexandre P Moulin, Louisa Koutroumanou, George Papadakis,Andrew C Browning, Savita Madhusudhan, Lotta Gränse,Eyal Banin,Ana Berta Sousa, Luisa Coutinho Santos, Laura Kuehlewein, Pietro De Angeli,Bart P Leroy,Omar A Mahroo, Fay Sedgwick, James Eden,Maximilian Pfau,Sten Andréasson,Hendrik P N Scholl,Carmen Ayuso,José M Millán,Dror Sharon,Miltiadis K Tsilimbaris,Veronika Vaclavik, Hoai V Tran, Tamar Ben-Yosef,Elfride De Baere,Andrew R Webster,Gavin Arno,Panagiotis I Sergouniotis,Susanne Kohl,Cristina Santos,Carlo Rivolta

American journal of human geneticsno. 4 (2025): 808-828

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A Novel Recurrent ARL3 Variant C.209g > A P.(gly70glu) Causes Variable Non-Syndromic Dominant Retinal Dystrophy with Defective Lipidated Protein Transport in Human Retinal Stem Cell Models

Julio C Corral-Serrano,Veronika Vaclavik,Stijn Van de Sompele,Karolina Kaminska,Katarina Jovanovic,Pascal Escher, Filip Van den Broeck,Francesca Cancellieri, Vasileios Toulis,Bart P Leroy,Julie de Zaeytijd, Zhixuan You,Daniele Ottaviani,Mathieu Quinodoz, Gabriela Bordeanu,Alison J Hardcastle,Frauke Coppieters,Viet H Tran,Michael E Cheetham,Carlo Rivolta,Elfride De Baere

Human molecular geneticsno. 9 (2025): 821-834

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Characterising the Refractive Error in Paediatric Patients with Congenital Stationary Night Blindness: a Multicentre Study

Austin D. Igelman,Elizabeth White,Alaa Tayyib,Lesley Everett,Ajoy Vincent,Elise Heon,Christina Zeitz,Michel Michaelides,Omar A. Mahroo,Mohamed Katta,Andrew Webster,Markus Preising,Birgit Lorenz,Samer Khateb,Eyal Banin,Dror Sharon, Shahar Luski,Filip Van Den Broeck,Bart Peter Leroy,Elfride De Baere,Sophie Walraedt,Katarina Stingl,Laura Kuehlewein,Susanne Kohl,Milda Reith,Anne Fulton,Aparna Raghuram,Isabelle Meunier,Helene Dollfus,Tomas S. Aleman,Emma C. Bedoukian,Erin C. O'Neil,Emily Krauss,Andrea Vincent,Charlotte Jordan,Alessandro Iannaccone,Parveen Sen,Srilekha Sundaramurthy,Soumittra Nagasamy,Irina Balikova,Ingele Casteels,Shyamanga Borooah,Shaden Yassin,Aaron Nagiel,Hillary Schwartz,Xavier Zanlonghi,Irene Gottlob,Rebecca J. Mclean,Francis L. Munier,Andrew Stephenson,Robert Sisk,Robert Koenekoop,Lorri B. Wilson,Douglas Fredrick,Dongseok Choi,Paul Yang,Mark Edward Pennesi

The British journal of ophthalmologyno. 2 (2025): 286-292

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Long‐term Results of Unilateral or Bilateral Injection of Lenadogene Nolparvovec Gene Therapy for Leber Hereditary Optic Neuropathy

Valérie Biousse,Patrick Yu‐Wai‐Man,Nancy Newman,Prem Subramanian,Mark Moster,An‐Guor Wang,Sean Donahue,Bart Leroy,Valerio Carelli,Catherine Vignal‐Clermont,Alfredo Sadun,Robert Sergott,Gema Rebolleda Fernández,Bart Chwalisz,Rudrani Banik,Magali Taiel,José‐Alain Sahel

Acta Ophthalmologicano. S284 (2025)

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Visual Acuity Outcomes by Causative Mutation in the Natural History of Leber Hereditary Optic Neuropathy: Analysis of Historical Data from Case Record Survey‐2 (CRS‐2)

Patrick Yu‐Wai‐Man, Judith van Everdingen,Bart Leroy, Maciej Krawczynski,Costanza Lamperti,Valerio Carelli,Xavier Llòria,Thomas Klopstock

Acta Ophthalmologicano. S284 (2025)

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INHERITED RETINAL DISEASE GENE PANEL IN POSTERIOR OR PANUVEITIS WITH DYSTROPHIC FEATURES

Stéphane Abramowicz,Audrey Meunier,Dafina Draganova,Laure Caspers,Marieke De Bruyne,Stijn Van de Sompele,Elfride De Baere,Bart P Leroy,Laurence Postelmans,François Willermain

Retina (Philadelphia, Pa)no. 3 (2025): 509-521

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THE FIGHT INHERITED RETINAL BLINDNESS! PROJECT

Matthew P. Simunovic,Anthony T. Moore,John Grigg,Panagiotis Sergouniotis,Omar A. Mahroo,Andrea Vincent,Mandeep Singh,M. Dominik Fischer,Thomas Edwards,Heather Mack, Michael Hogden,Fred K. Chen,Alex Hewitt,Lauren Ayton,Bart Leroy,Robyn Jamieson,Mark C. Gillies,Daniel Barthelmes

RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASESno. 2 (2025): 286-295

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Visual Acuity Outcomes by Causative Mutation in the Natural History of Leber Hereditary Optic Neuropathy: Analysis of Historical Data from Case Record Survey‐2 (CRS‐2)

Patrick Yu‐Wai‐Man, Judith van Everdingen,Bart Leroy, Maciej Krawczynski,Costanza Lamperti,Valerio Carelli,Xavier Llòria,Thomas Klopstock

Acta Ophthalmologicano. S284 (2025)

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Visual Acuity Outcomes by Sex in a Historical Population of Patients with Leber Hereditary Optic Neuropathy from Case Record Survey‐2 (CRS‐2)

Marcela Votruba,Bart Leroy,Patrick Yu‐Wai‐Man, Judith Van Everdingen, Maciej Krawczynski,Costanza Lamperti,Valerio Carelli,Xavier Llòria,Thomas Klopstock

Acta Ophthalmologicano. S284 (2025)

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Gene Therapy-Associated Uveitis (GTAU): Understanding and Mitigating the Adverse Immune Response in Retinal Gene Therapy

Ryan Purdy, Molly John, Alissa Bray, Alison J Clare,David A Copland,Ying Kai Chan, Robert H Henderson,Fanny Nerinckx,Bart P Leroy,Paul Yang,Mark E Pennesi,Robert E MacLaren,M Dominik Fischer,Andrew D Dick,Kanmin Xue

Progress in retinal and eye research（2025）

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Papers共 403 篇Author StatisticsCo-AuthorSimilar Experts