| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Louise Porter | Q55711181 |
| Graeme Black | Q30429957 | ||
| P2093 | author name string | L F Porter | |
| P2860 | cites work | Recommendations for Genetic Testing of Inherited Eye Diseases | Q57784447 |
| Initial sequencing and analysis of the human genome | Q21045365 | ||
| A comprehensive review of retinal gene therapy | Q27023914 | ||
| Effect of gene therapy on visual function in Leber's congenital amaurosis | Q28277981 | ||
| The significance of the complement system for the pathogenesis of age-related macular degeneration - current evidence and translation into clinical application | Q34588115 | ||
| Genetic insights into age-related macular degeneration: controversies addressing risk, causality, and therapeutics | Q36084168 | ||
| Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement | Q36598421 | ||
| Genetic counseling and genetic testing in ophthalmology | Q37557279 | ||
| Next-generation sequencing in the clinic: promises and challenges | Q38061737 | ||
| Impact of new genomic tools on the practice of clinical genetics in consanguineous populations: the Saudi experience | Q38085625 | ||
| The future of technologies for personalised medicine | Q39532001 | ||
| Lake Louise mutation detection meeting 2013: clinical translation of next-generation sequencing requires optimization of workflows and interpretation of variants | Q42630382 | ||
| Genetic influences on the outcome of anti-vascular endothelial growth factor treatment in neovascular age-related macular degeneration | Q44245879 | ||
| A paradigm shift in the delivery of services for diagnosis of inherited retinal disease | Q45879073 | ||
| Genetic testing for inherited eye disease: who benefits? | Q46957887 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P921 | main subject | eye disease | Q3041498 |
| ophthalmology | Q161437 | ||
| gene therapy | Q213901 | ||
| biomedical investigative technique | Q66648976 | ||
| molecular diagnostic techniques | Q69527481 | ||
| precision medicine | Q17075943 | ||
| P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
| P304 | page(s) | 1-11 | |
| P577 | publication date | 2014-07-01 | |
| P1433 | published in | Clinical Genetics | Q5133760 |
| P1476 | title | Personalized ophthalmology | |
| P478 | volume | 86 |
| Q92914602 | A new paradigm for delivering personalised care: integrating genetics with surgical interventions in BEST1 mutations |
| Q36773888 | Age-related macular degeneration: genome-wide association studies to translation. |
| Q37609515 | An Ocular Protein Triad Can Classify Four Complex Retinal Diseases. |
| Q35805426 | Improvement in vision: a new goal for treatment of hereditary retinal degenerations |
| Q30408185 | Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results |
| Q61448666 | Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes |
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