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B

Bart P. Leroy

Department of Ophthalmology

55H指数
380论文数
1.3W被引数
收录论文 143
发表时间
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Launching a multi-level data strategy for rare eye diseases: a methodological case study from national to European scale为罕见眼病制定多层级数据战略：从国家到欧洲层面的方法学案例研究
errOrphanet Journal of Rare Diseases
IF3.5
err2026-07-21
err0
errOAAI
errCamille Beluffi-Marin; Marilyne Oswald; Isabella Anna Vacchi; David Keegan; Bart Peter Leroy; Hélène Dollfus
err分享
err收藏
Expert Consensus on Characteristics, Etiology, and Management of Chorioretinal Atrophy in Patients Treated with Voretigene Neparvovec专家共识：经Voretigene Neparvovec治疗患者的脉络膜视网膜萎缩特征、病因及管理
errOphthalmology Science
IF4.6
err2026-01-29
err0
errOAAI
errM Dominik Fischer; Isabelle Audo; David Gaucher; Frank G. Holz; Line Kessel; Stephen Russell; Katarina Stingl; David L. Rousso; Rainer Maier; Andreas Clemens; Aaron Nagiel; Bart P. Leroy
err分享
err收藏
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosaU4和U6 snRNA基因的新生和遗传显性变异导致色素性视网膜炎
errNature Genetics
IF29
err2026-01-09
err0
errOAAI
errMathieu Quinodoz; Kim Rodenburg; Zuzana Cvackova; Karolina Kaminska; Suzanne E. de Bruijn; Ana Belén Iglesias-Romero; Erica G. M. Boonen; Mukhtar Ullah; Nick Zomer; Marc Folcher; Jacques Bijon; Lara K. Holtes; Stephen H. Tsang; Zelia Corradi; K. Bailey Freund; Stefanida Shliaga; Daan M. Panneman; Rebekkah J. Hitti-Malin; Manir Ali; Ala’a AlTalbishi; Sten Andréasson; Georg Ansari; Gavin Arno; Galuh D. N. Astuti; Carmen Ayuso; Radha Ayyagari; Sandro Banfi; Eyal Banin; Tahsin Stefan Barakat; Mirella T. S. Barboni; Miriam Bauwens; Tamar Ben-Yosef; Virginie Bernard; David G. Birch; Pooja Biswas; Fiona Blanco-Kelly; Beatrice Bocquet; Camiel J. F. Boon; Kari Branham; Dominique Bremond-Gignac; Alexis Ceecee Britten-Jones; Kinga M. Bujakowska; Cyril Burin des Roziers; Elizabeth L. Cadena; Giacomo Calzetti; Francesca Cancellieri; Luca Cattaneo; Naomi Chadderton; Peter Charbel Issa; Luísa Coutinho-Santos; Stephen P. Daiger; Elfride De Baere; Marieke De Bruyne; Berta de la Cerda; John N. De Roach; Julie De Zaeytijd; Ronny Derks; Claire-Marie Dhaenens; Lubica Dudakova; Jacque L. Duncan; G. Jane Farrar; Nicolas Feltgen; Beau J. Fenner; Lidia Fernández-Caballero; Juliana M. Ferraz Sallum; Simone Gana; Alejandro Garanto; Jessica C. Gardner; Christian Gilissen; Roser Gonzàlez-Duarte; Kensuke Goto; Sam Griffiths-Jones; Tobias B. Haack; Lonneke Haer-Wigman; Alison J. Hardcastle; Takaaki Hayashi; Elise Héon; Lies H. Hoefsloot; Alexander Hoischen; Josephine P. Holtan; Carel B. Hoyng; Manuel Benjamin B. Ibanez; Chris F. Inglehearn; Takeshi Iwata; Brynjar O. Jensson; Kaylie Jones; Vasiliki Kalatzis; Smaragda Kamakari; Marianthi Karali; Ulrich Kellner; Caroline C. W. Klaver; Krisztina Knézy; Robert K. Koenekoop; Susanne Kohl; Taro Kominami; Laura Kühlewein; Tina M. Lamey; Rina Leibu; Bart P. Leroy; Petra Liskova; Irma Lopez; Victor R. de J. López-Rodríguez; Quinten Mahieu; Omar A. Mahroo; Gaël Manes; Luke Mansard; M. Pilar Martín-Gutiérrez; Nelson Martins; Laura Mauring; Martin McKibbin; Terri L. McLaren; Isabelle Meunier; Michel Michaelides; José M. Millán; Kei Mizobuchi; Rajarshi Mukherjee; Zoltán Zsolt Nagy; Kornelia Neveling; Monika Ołdak; Michiel Oorsprong; Yang Pan; Anastasia Papachristou; Antonio Percesepe; Maximilian Pfau; Eric A. Pierce; Emily Place; Raj Ramesar; Francis Ramond; Florence Andrée Rasquin; Gillian I. Rice; Lisa Roberts; María Rodríguez-Hidalgo; Javier Ruiz-Ederra; Ataf H. Sabir; Ai Fujita Sajiki; Ana Isabel Sánchez-Barbero; Asodu Sandeep Sarma; Riccardo Sangermano; Cristina M. Santos; Margherita Scarpato; Hendrik P. N. Scholl; Dror Sharon; Sabrina G. Signorini; Francesca Simonelli; Ana Berta Sousa; Maria Stefaniotou; Kari Stefansson; Katarina Stingl; Akiko Suga; Patrick Sulem; Lori S. Sullivan; Viktória Szabó; Jacek P. Szaflik; Gita Taurina; Alberta A. H. J. Thiadens; Carmel Toomes; Viet H. Tran; Miltiadis K. Tsilimbaris; Pavlina Tsoka; Veronika Vaclavik; Marie Vajter; Sandra Valeina; Enza Maria Valente; Casey Valentine; Rebeca Valero; Sophie Valleix; Joseph van Aerschot; L. Ingeborgh van den Born; Mattias Van Heetvelde; Virginie J. M. Verhoeven; Andrea L. Vincent; Andrew R. Webster; Laura Whelan; Bernd Wissinger; Georgia G. Yioti; Kazutoshi Yoshitake; Juan C. Zenteno; Roberta Zeuli; Theresia Zuleger; Chaim Landau; Allan I. Jacob; Siying Lin; Frans P. M. Cremers; Winston Lee; Jamie M. Ellingford; David Stanek; Susanne Roosing; Carlo Rivolta
err分享
err收藏
Generation and characterization of three human induced pluripotent stem cell lines (UGENTi005, UGENTi006 and UGENTi007) from patients with autosomal dominant adult-onset maculopathy due to RPE65 variant c.1555G>A, p.(E519K)
errSTEM CELL RESEARCH
IF0.7
err2025-11-01
err0
errOAAI
errVan Vooren, Eline; Van den Broeck, Filip; Daal, Esperanza; Ghazvini, Mehrnaz; De Zaeytijd, Julie; Leroy, Bart P.; Bauwens, Miriam; De Baere, Elfride
err分享
err收藏
Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisisX连锁视网膜劈裂患者的玻璃体视网膜并发症及手术结果
errACTA OPHTHALMOLOGICA
IF2.8
err2025-11-01
err0
errOAAI
errHensman, Jonathan; Hahn, Leo C.; van Schooneveld, Mary J.; Diederen, Roselie M. H.; van den Broeck, Filip; Ten Brink, Jacoline B.; Thiadens, Alberta A.; van Genderen, Maria M.; van den Born, L. Ingeborgh; Leroy, Bart P.; Hoyng, Carel B.; Boon, Camiel J. F.
err分享
err收藏
Quality of life in children and adolescents with visual impairment: key pillars of support explored through a qualitative analysis among different healthcare professionals in the Flemish healthcare landscape视障儿童和青少年的生活质量：在弗拉芒医疗保健体系中，通过对不同医疗保健专业人员进行定性分析所探索的支持关键支柱
errDISABILITY AND REHABILITATION
IF2
err2025-10-01
err0
PREAI
errSlaghmuylder, Yael; Lauwerier, Emelien; Leroy, Bart P.
err分享
err收藏
Gene Therapy-Associated Uveitis (GTAU): Understanding and mitigating the adverse immune response in retinal gene therapy基因治疗相关葡萄膜炎(GTAU)：理解并减轻视网膜基因治疗中的不良免疫反应
errPROGRESS IN RETINAL AND EYE RESEARCH
IF14.7
err2025-05-01
err1
errOAAI
errPurdy, Ryan; John, Molly; Bray, Alissa; Clare, Alison J.; Copland, David A.; Chan, Ying Kai; Henderson, Robert H.; Nerinckx, Fanny; Leroy, Bart P.; Yang, Paul; Pennesi, Mark E.; Maclaren, Robert E.; Fischer, M. Dominik; Dick, Andrew D.
err分享
err收藏
Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2025-04-01
err0
errOAAI
errKaminska, Karolina; Cancellieri, Francesca; Quinodoz, Mathieu; Moye, Abigail R.; Bauwens, Miriam; Lin, Siying; Janeschitz-Kriegl, Lucas; Hayman, Tamar; Barberan-Martinez, Pilar; Schlaeger, Regina; van den Broeck, Filip; Fernandez, Almudena Avila; Fernandez-Caballero, Lidia; Perea-Romero, Irene; Garcia-Garcia, Gema; Salom, David; Mazzola, Pascale; Zuleger, Theresia; Poths, Karin; Haack, Tobias B.; Jacob, Julie; Vermeer, Sascha; Terbeek, Frederique; Feltgen, Nicolas; Moulin, Alexandre P.; Koutroumanou, Louisa; Papadakis, George; Browning, Andrew C.; Madhusudhan, Savita; Granse, Lotta; Banin, Eyal; Sousa, Ana Berta; Santos, Luisa Coutinho; Kuehlewein, Laura; De Angeli, Pietro; Leroy, Bart P.; Mahroo, Omar A.; Sedgwick, Fay; Eden, James; Pfau, Maximilian; Andreasson, Sten; Scholl, Hendrik P. N.; Ayuso, Carmen; Millan, Jose M.; Sharon, Dror; Tsilimbaris, Miltiadis K.; Vaclavik, Veronika; Tran, Hoai, V; Ben-Yosef, Tamar; De Baere, Elfride; Webster, Andrew R.; Arno, Gavin; Sergouniotis, Panagiotis I.; Kohl, Susanne; Santos, Cristina; Rivolta, Carlo
err分享
err收藏
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
errHUMAN MOLECULAR GENETICS
IF3.2
err2025-03-01
err0
errOAAI
errCorral-Serrano, Julio C.; Vaclavik, Veronika; van de Sompele, Stijn; Kaminska, Karolina; Jovanovic, Katarina; Escher, Pascal; van den Broeck, Filip; Cancellieri, Francesca; Toulis, Vasileios; Leroy, Bart P.; de Zaeytijd, Julie; You, Zhixuan; Ottaviani, Daniele; Quinodoz, Mathieu; Bordeanu, Gabriela; Hardcastle, Alison J.; Coppieters, Frauke; Tran, Viet H.; Cheetham, Michael E.; Rivolta, Carlo; De Baere, Elfride
err分享
err收藏
Visual acuity outcomes by sex in a historical population of patients with leber hereditary optic neuropathy from case record survey-2 (CRS-2)莱伯遗传性视神经病变历史患者群体中，按性别划分的视力矫正结果（基于病例记录调查-2（CRS-2））
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errVotruba, M; Leroy, B; Yu-Wai-Man, P; Van Everdingen, J; Krawczynski, M; Lamperti, C; Carelli, V; Llória, X; Klopstock, T
err分享
err收藏
Long-term results of unilateral or bilateral injection of lenadogene nolparvovec gene therapy for leber hereditary optic neuropathy单侧或双侧注射lenadogene nolparvovec基因疗法治疗Leber遗传性视神经病变的长期结果
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errBiousse, V; Yu-Wai-Man, P; Newman, N; Subramanian, P; Moster, M; Wang, AG; Donahue, S; Leroy, B; Carelli, V; Vignal-Clermont, C; Sadun, A; Sergott, R; Fernández, GR; Chwalisz, B; Banik, R; Taiel, M; Sahel, JA
err分享
err收藏
Long-term results of unilateral or bilateral injection of lenadogene nolparvovec gene therapy for leber hereditary optic neuropathy单侧或双侧注射lenadogene nolparvovec基因疗法治疗莱伯遗传性视神经病变的长期结果
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errBiousse, V; Yu-Wai-Man, P; Newman, N; Subramanian, P; Moster, M; Wang, AG; Donahue, S; Leroy, B; Carelli, V; Vignal-Clermont, C; Sadun, A; Sergott, R; Fernández, GR; Chwalisz, B; Banik, R; Taiel, M; Sahel, JA
err分享
err收藏
Changes in visual acuity categories in a historical population of patients with leber hereditary optic neuropathy from case record survey-2 (CRS-2)Leber遗传性视神经病变患者历史人群的视力类别变化：来自病例记录调查-2 (CRS-2) 的数据
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errKlopstock, T; Leroy, B; Yu-Wai-Man, P; van Everdingen, J; Krawczynski, M; Lamperti, C; Carelli, V; Llória, X
err分享
err收藏
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)视敏度结局按致病突变在莱伯遗传性视神经病变的自然史中的分析：来自病例记录调查-2（CRS-2）历史数据的分析
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errYu-Wai-Man, P; van Everdingen, J; Leroy, B; Krawczynski, M; Lamperti, C; Carelli, V; Llòria, X; Klopstock, T
err分享
err收藏
Visual acuity outcomes by age at symptom onset in the natural history of leber hereditary optic neuropathy: Analysis of historical data from Case Record Survey-2 (CRS-2)视敏度结局与症状起始年龄在Leber遗传性视神经病变自然史中的关系：对Case Record Survey-2 (CRS-2)历史数据的分析
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errLlòria, X; Yu-Wai-Man, P; van Everdingen, J; Leroy, B; Krawczynski, M; Lamperti, C; Carelli, V; Klopstock, T
err分享
err收藏
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)视锐度结局与致病突变在Leber遗传性视神经病变自然史中的关系：Case Record Survey-2 (CRS-2)历史数据分析
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errYu-Wai-Man, P; Van Everdingen, J; Leroy, B; Krawczynski, M; Lamperti, C; Carelli, V; Llòria, X; Klopstock, T
err分享
err收藏
Visual acuity outcomes by age at symptom onset in the natural history of leber hereditary optic neuropathy: Analysis of historical data from Case Record Survey-2 (CRS-2)根据症状起始年龄的莱伯遗传性视神经病变自然史中的视敏度结果：对Case Record Survey-2 (CRS-2)历史数据的分析
errACTA OPHTHALMOLOGICA
IF2.8
err2025-01-19
err0
PREAI
errLlòria, X; Yu-Wai-Man, P; Van Everdingen, J; Leroy, B; Krawczynski, M; Lamperti, C; Carelli, V; Klopstock, T
err分享
err收藏
Automated Cone Photoreceptor Detection in Adaptive Optics Flood Illumination Ophthalmoscopy
errOPHTHALMOLOGY SCIENCE
IF4.6
err2024-12-01
err0
PREAI
errWooning, Sander; Heutinck, Pam A. T.; Liman, Kubra; Hennekam, Sem; van Haute, Manon; van den Broeck, Filip; Leroy, Bart; Sampson, Danuta M.; Roshandel, Danial; Chen, Fred K.; Pelt, Daniel M.; van den Born, L. Ingeborgh; Verhoeven, Virginie J. M.; Klaver, Caroline C. W.; Thiadens, Alberta A. H. J.; Durand, Marine; Chateau, Nicolas; van Walsum, Theo; De Jesus, Danilo Andrade; Brea, Luisa Sanchez
err分享
err收藏
Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy
errSCIENTIFIC REPORTS
IF3.9
err2024-10-03
err1
errOAAI
errde Muijnck, Cansu; Haer-Wigman, Lonneke; van Everdingen, Judith A. M.; Lushchyk, Tanya; Heutinck, Pam A. T.; van Dooren, Marieke F.; Kievit, Anneke J. A.; Verhoeven, Virginie J. M.; Simon, Marleen E. H.; Wasmann, Rosemarie A.; Notting, Irene C.; De Baere, Elfride; Walraedt, Sophie; De Zaeytijd, Julie; van den Broeck, Filip; Leroy, Bart P.; Boon, Camiel J. F.; van Genderen, Maria M.
err分享
err收藏
Practice Patterns and Challenges in Managing Inherited Retinal Diseases Across Asia-Pacific: A Survey from the APIED Network亚太地区遗传性视网膜疾病管理的实践模式和挑战: 来自APIED网络的调查
errASIA-PACIFIC JOURNAL OF OPHTHALMOLOGY
IF4.5
err2024-09-01
err0
errOAAI
errWong, Wendy M.; Tham, Yih Chung; Ayton, Lauren N.; Britten-Jones, Alexis Ceecee; Edwards, Thomas L.; Grigg, John; Simunovic, Matthew P.; Chen, Fred K.; Jin, Zi-Bing; Shen, Ren-Juan; Sui, Ruifang; Yang, Liping; Zhao, Chen; Chen, Haoyu; Li, Shiying; Ding, Xiaoyan; Bhende, Muna; Raman, Rajiv; Sen, Parveen; Poornachandra, B.; Chia, Valen; Manurung, Florence; Sasongko, Muhammad Bayu; Ikeda, Hanako; Fujinami, Kaoru; Woo, Se Joon; Kim, Sang Jin; Bastion, Mae-Lynn Catherine; Kamalden, Ain Tengku; Lott, Penny P.; Fong, Kenneth; Shunmugam, Manoharan; Lim, Amelia; Thapa, Raba; Ibanez, B. Manuel Benjamin; Koh, Adrian; Holder, Graham E.; Su, Xinyi; Chan, Choi Mun; Fenner, Beau J.; Laude, Augustinus; Ngo, Wei Kiong; Chen, Ta-Ching; Wang, Nan-Kai; Kang, Eugene Yu-Chuan; Surawatsatien, Nuntachai; Pisuchpen, Phattrawan; Sujirakul, Tharikarn; Wongchaisuwat, Nida; Apivatthakakul, Atitaya; Kumaramanickavel, Govindasamy; Leroy, Bart; Michaelides, Michel; Pontikos, Nikolas; Cheng, Ching-Yu; Pang, Chi Pui; Chen, Li Jia; Chan, Hwei Wuen
err分享
err收藏

研究方向

暂无研究方向
合作学者
合作期刊
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H 指数: 141 · 论文数: 325
Y
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H 指数: 133 · 论文数: 770
C
Claus Bachert
H 指数: 132 · 论文数: 1.3K
J
Jeroen Raes
H 指数: 127 · 论文数: 465
B
Bart N. Lambrecht
H 指数: 123 · 论文数: 761
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