ORA - Oxford University Research Archive

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1

Journal article

A qualitative and quantitative assessment of fundus autofluorescence patterns in patients with choroideremia

Jolly, J, Edwards, TL, Moules, J, et al.
2016-08-01

2

Journal article

Autosomal-dominant corneal endothelial dystrophies CHED1 and PPCD1 are allelic disorders caused by non-coding mutations in the promoter of OVOL2

Davidson, AE, Liskova, P, Evans, CJ, et al.
2015-12-31

3

Journal article

Visual acuity after retinal gene therapy for Choroideremia

Edwards, TL, Jolly, JK, Groppe, M, et al.
2016-05-19

4

Journal article

Impact of vital dyes on cell viability and transduction efficiency of AAV vectors used in retinal gene therapy surgery: an in vitro and in vivo analysis

Salvetti, AP, Patrício, MI, Barnard, AR, et al.
2017-07-10

5

Journal article

Unravelling the genetics of inherited retinal dystrophies: Past, present and future.

Broadgate, S, Yu, J, Downes, SM, et al.
2017-03-05

6

Journal article

Combining M-FISH and Quantum Dot technology for fast chromosomal assignment of transgenic insertions.

Yusuf, M, Bauer, DL, Lipinski, DM, et al.
2011-01-01

7

Journal article

De novo mutations in EBF3 cause a neurodevelopmental syndrome

Sleven, H, Welsh, SJ, Yu, J, et al.
2016-12-23

8

Journal article

Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data

Pontikos, N, Yu, J, Moghul, I, et al.
2017-03-15

9

Journal article

Single residue AAV capsid mutation improves transduction of photoreceptors in the Abca4-/- mouse and bipolar cells in the rd1 mouse and human retina ex-vivo

De Silva, SR, Charbel Issa, P, Singh, MS, et al.
2016-08-11

10

Journal article

Cone fusion confusion in photoreceptor transplantation

MacLaren, RE
2017-08-29

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