Genetics of the Retinal Dystrophies by Merepa, S, Broadgate, S, Sekaran, S, Halford, S

Unravelling the genetics of inherited retinal dystrophies: Past, present and future. by Broadgate, S, Yu, J, Downes, S, Halford, S

Diabetic macular oedema: under‐represented in the genetic analysis of diabetic retinopathy by Broadgate, S, Kiire, C, Halford, S, Chong, V

Factors affecting snow damage of trees with particular reference to European conditions by Marja-Leena Nykänen, Marianne Broadgate, Seppo Kellomäki, Heli Peltola, Christopher Quine

Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy by Singh, M, Broadgate, S, Mathur, R, Holt, R, Halford, S, MacLaren, R

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

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

Intraretinal Microvascular Abnormalities and Venous Beading Have Different Genetic Profiles in Caucasian Patients with Non-Proliferative Diabetic Retinopathy by Elizabeth Pearce, Sobha Sivaprasad, Suzanne Broadgate, Christine Kiire, Susan M. Downes, Stephanie Halford, Victor Chong

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"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

An Overview of the Genetics of <i>ABCA4</i> Retinopathies, an Evolving Story by Saoud Al-Khuzaei, Suzanne Broadgate, Charlotte R. Foster, Mital Shah, Jing Yu, Susan M. Downes, Stephanie Halford

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Novel Pathogenic Sequence Variants in <i>NR2E3</i> and Clinical Findings in Three Patients by Saoud Al-khuzaei, Suzanne Broadgate, Stephanie Halford, Jasleen K. Jolly, Morag Shanks, Penny Clouston, Susan M. Downes

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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

Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2. by Inglis-Broadgate, S, Ocaka, L, Banerjee, R, Gaasenbeek, M, Chapple, J, Cheetham, M, Clark, B, Hunt, D, Halford, S

New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders by R. Holt, F. Ceroni, D. A. Bax, S. Broadgate, D. Gold Diaz, C. Santos, D. Gerrelli, N. K. Ragge

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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

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

Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy – a case report by Saoud Al-Khuzaei, Karl A. Z. Hudspith, Suzanne Broadgate, Morag E. Shanks, Penny Clouston, Andrea H. Németh, Stephanie Halford, Susan M. Downes

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Characterization of CDH3-related congenital hypotrichosis with juvenile macular dystrophy by Hull, S, Arno, G, Robson, A, Broadgate, S, Plagnol, V, McKibbin, M, Halford, S, Michaelides, M, Holder, G, Moore, A, Khan, K, Webster, A