Adaptive optics scanning laser ophthalmoscopy in a heterogenous cohort with Stargardt disease by Shah, M, Downes, SM, Smithson, HE, Young, LK

The incidence, monitoring coverage and clinical characteristics of hydroxychloroquine retinopathy in the United Kingdom by Yusuf, IH, Han, RC, Downes, SM, Sharma, SM

Hydroxychloroquine hitting the headlines: Retinal considerations by Downes, SM, Leroy, BP, Sharma, SM, Sivaprasad, S, Dollfus, H

The role of multimodal imaging and vision function testing in ABCA4-related retinopathies and their relevance to future therapeutic interventions by Al-Khuzaei, S, Shah, M, Foster, CR, Yu, J, Broadgate, S, Halford, S, Downes, SM

Novel pathogenic sequence variants in NR2E3 and clinical findings in three patients by Al-Khuzaei, S, Broadgate, S, Halford, S, Jolly, JK, Shanks, M, Clouston, P, Downes, SM

An overview of the genetics of ABCA4 retinopathies, an evolving story by Al-Khuzaei, S, Broadgate, S, Foster, CR, Shah, M, Yu, J, Downes, SM, Halford, S

Rapid Quantification of the Binocular Visual Field for Clinical Trials: Performance of a Modified Esterman Supra-Threshold Test Implemented with the Open Perimetry Interface by Andrews CD, Sheldon AA, Bridge H, Downes SM, MacLaren RE, Jolly JK

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Rapid quantification of the binocular visual field for clinical trials: performance of a modified Esterman supra-threshold test implemented with the open perimetry interface by Andrews, CD, Sheldon, AA, Bridge, H, Downes, SM, MacLaren, RE, Jolly, JK

Combined central serous chorioretinopathy, hypermetropia, short axial length, chorioretinal folds, enlarged/thickened ocular coats, with varying association of scleral changes (CHA... by Downes, SM, Mall, SP, Al-Khuzaei, S, Chadha, R, Gibson, A, Chong, V, Bird, AC

Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy - a case report by Al-Khuzaei, S, Hudspith, KAZ, Broadgate, S, Shanks, ME, Clouston, P, Németh, AH, Halford, S, Downes, SM

"Genetic and clinical findings in an ethnically diverse retinitis pigmentosa cohort associated with pathogenic variants in EYS" by Cundy, O, Broadgate, S, Halford, S, MacLaren, RE, Shanks, ME, Clouston, P, Gilhooley, MJ, Downes, SM

Clinical characterization of retinitis pigmentosa associated with variants in SNRNP200 by Yusuf, IH, Birtel, J, Shanks, ME, Clouston, P, Downes, SM, Charbel Issa, P, MacLaren, RE

Retinitis pigmentosa caused by variants in SNRNP200 by Yusuf, IH, Birtel, J, Shanks, M, Clouston, P, Downes, SM, Charbel Issa, P, MacLaren, RE

Association of clinical and genetic heterogeneity with BEST1 sequence variations by Shah, M, Broadgate, S, Shanks, M, Clouston, P, Yu, J, MacLaren, RE, Németh, AH, Halford, S, Downes, SM

An audit of the use of hydroxychloroquine in rheumatology clinics by Worth, C, Yusuf, IH, Turner, B, Gourier, H, Brooks, EE, Mort, DO, Sharma, S, Downes, SM, Luqmani, RA

Pigmentary retinopathy, rod-cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNA(Lys) (m.8340G>A) gene variant. by Gill, JS, Hardy, SA, Blakely, EL, Hopton, S, Nemeth, AH, Fratter, C, Poulton, J, Taylor, RW, Downes, SM

Genetic and clinical findings in an ethnically diverse cohort with Retinitis Pigmentosa associated with pathogenic variants in CERKL by Downes, SM, Nguyen, T, Tai, V, Broadgate, S, Shah, M, Al-Khuzaei, S, MacLaren, RE, Shanks, M, Clouston, P, Halford, S

Age-related macular degeneration: suitability of optogenetic therapy for geographic atrophy by Borchert, GA, Shamsnajafabadi, H, Ng, BWJ, Xue, K, De Silva, SR, Downes, SM, MacLaren, RE, Cehajic-Kapetanovic, J

Chronic central serous chorioretinopathy: long-term follow-up and vision-related quality of life by Breukink MB, Dingemans AJM, den Hollander AI, Keunen JEE, MacLaren RE, Fauser S, Querques G, Hoyng CB, Downes SM, Boon CJF

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Phenotypic and genetic characteristics in a cohort of patients with Usher genes by Feenstra, HM, Shah, M, Broadgate, S, Shanks, M, Kamath, A, Yu, J, Jolly, JK, MacLaren, RE, Clouston, P, Halford, S, Downes, SM