CUGC for congenital primary aphakia

le Sarkar, Hajrah, Moore, William, Leroy, Bart P, Moosajee, Mariya
Foilsithe in Eur J Hum Genet (2018)

Hydroxychloroquine hitting the headlines—retinal considerations

le Downes, Susan M., Leroy, Bart P., Sharma, Srilakshmi M., Sivaprasad, Sobha, Dollfus, Hélène
Foilsithe in Eye (Lond) (2020)

Vitreous Hemorrhage as Presenting Sign of Retinal Arteriovenous Malformation

le Accou, Geraldine P. B. M., Nerinckx, Fanny, Leroy, Bart P., De Zaeytijd, Julie
Foilsithe in Case Rep Ophthalmol Med (2020)

Clinical Perspective: Treating RPE65-Associated Retinal Dystrophy

le Maguire, Albert M., Bennett, Jean, Aleman, Elena M., Leroy, Bart P., Aleman, Tomas S.
Foilsithe in Mol Ther (2021)

An update on the ocular phenotype in patients with pseudoxanthoma elasticum

le Gliem, Martin, Zaeytijd, Julie De, Finger, Robert P., Holz, Frank G., Leroy, Bart P., Issa, Peter Charbel
Foilsithe 2013

Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies)

le Ramsden, Simon C, Davidson, Alice E, Leroy, Bart P, Moore, Anthony T, Webster, Andrew R, Black, Graeme C M, Manson, Forbes D C
Foilsithe 2012

Detailed Functional and Structural Phenotype of Bietti Crystalline Dystrophy Associated with Mutations in CYP4V2 Complicated by Choroidal Neovascularization

le Fuerst, Nicole M., Serrano, Leona, Han, Grace, Morgan, Jessica I. W., Maguire, Albert M., Leroy, Bart P., Kim, Benjamin J., Aleman, Tomas S.
Foilsithe in Ophthalmic Genet (2016)

The N‐terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond

le Naessens, Sarah, De Zaeytijd, Julie, Syx, Delfien, Vandenbroucke, Roosmarijn E., Smeets, Frédéric, Van Cauwenbergh, Caroline, Leroy, Bart P., Peelman, Frank, Coppieters, Frauke
Foilsithe in Hum Mutat (2019)

Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7

le Van Schil, Kristof, Karlstetter, Marcus, Aslanidis, Alexander, Dannhausen, Katharina, Azam, Maleeha, Qamar, Raheel, Leroy, Bart P., Depasse, Fanny, Langmann, Thomas, De Baere, Elfride
Foilsithe in Sci Rep (2016)

Recurrent Mutation in the First Zinc Finger of the Orphan Nuclear Receptor NR2E3 Causes Autosomal Dominant Retinitis Pigmentosa

le Coppieters, Frauke , Leroy, Bart P. , Beysen, Diane , Hellemans, Jan , De Bosscher, Karolien , Haegeman, Guy , Robberecht, Kirsten , Wuyts, Wim , Coucke, Paul J. , De Baere, Elfride 
Foilsithe 2007

Retinal Development in Infants and Young Children with Achromatopsia

le Lee, Helena, Purohit, Ravi, Sheth, Viral, McLean, Rebecca J., Kohl, Susanne, Leroy, Bart P., Sundaram, Venki, Michaelides, Michel, Proudlock, Frank A., Gottlob, Irene
Foilsithe in Ophthalmology (2015)

The importance of genetic testing as demonstrated by two cases of CACNA1F-associated retinal generation misdiagnosed as LCA

le Men, Clara J., Bujakowska, Kinga M., Comander, Jason, Place, Emily, Bedoukian, Emma C., Zhu, Xiaosong, Leroy, Bart P., Fulton, Anne B., Pierce, Eric A.
Foilsithe in Mol Vis (2017)

LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS—SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED: A Review

le Leroy, Bart P., Birch, David G., Duncan, Jacque L., Lam, Byron L., Koenekoop, Robert K., Porto, Fernanda B. O., Russell, Stephen R., Girach, Aniz
Foilsithe in Retina (2021)

Phenocopy of a heterozygous carrier of X-linked retinitis pigmentosa due to mosaicism for a RHO variant

le Strubbe, Ine, Van Cauwenbergh, Caroline, De Zaeytijd, Julie, De Jaegere, Sarah, De Bruyne, Marieke, Rosseel, Toon, Van de Sompele, Stijn, De Baere, Elfride, Leroy, Bart P.
Foilsithe in Sci Rep (2021)

A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy

le Mukhopadhyay, Rajarshi, Sergouniotis, Panagiotis I., Mackay, Donna S., Day, Alexander C., Wright, Genevieve, Devery, Sophie, Leroy, Bart P., Robson, Anthony G., Holder, Graham E., Li, Zheng, Webster, Andrew R.
Foilsithe 2010

The human visual cortex responds to gene therapy–mediated recovery of retinal function

le Ashtari, Manzar, Cyckowski, Laura L., Monroe, Justin F., Marshall, Kathleen A., Chung, Daniel C., Auricchio, Alberto, Simonelli, Francesca, Leroy, Bart P., Maguire, Albert M., Shindler, Kenneth S., Bennett, Jean
Foilsithe 2011

The human visual cortex responds to gene therapy–mediated recovery of retinal function

le Ashtari, Manzar, Cyckowski, Laura L., Monroe, Justin F., Marshall, Kathleen A., Chung, Daniel C., Auricchio, Alberto, Simonelli, Francesca, Leroy, Bart P., Maguire, Albert M., Shindler, Kenneth S., Bennett, Jean
Foilsithe 2011

Abnormal retinal development associated with FRMD7 mutations

le Thomas, Mervyn G., Crosier, Moira, Lindsay, Susan, Kumar, Anil, Araki, Masasuke, Leroy, Bart P., McLean, Rebecca J., Sheth, Viral, Maconachie, Gail, Thomas, Shery, Moore, Anthony T., Gottlob, Irene
Foilsithe 2014

Chromosomal Duplication Involving the Forkhead Transcription Factor Gene FOXC1 Causes Iris Hypoplasia and Glaucoma

le Lehmann, Ordan J., Ebenezer, Neil D., Jordan, Tim, Fox, Margaret, Ocaka, Louise, Payne, Annette, Leroy, Bart P., Clark, Brian J., Hitchings, Roger A., Povey, Sue, Khaw, Peng T., Bhattacharya, Shomi S.
Foilsithe 2000

Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy

le Bauwens, Miriam, Storch, Stephan, Weisschuh, Nicole, Ceuterick‐de Groote, Chantal, De Rycke, Riet, Guillemyn, Brecht, De Jaegere, Sarah, Coppieters, Frauke, Van Coster, Rudy, Leroy, Bart P., De Baere, Elfride
Foilsithe in Clin Genet (2019)