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Gerald Holder - Publications

Affiliations: 
University of Michigan, Ann Arbor, Ann Arbor, MI 
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5 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Ritter M, Arno G, Ba-Abbad R, Holder GE, Webster AR. Macular maldevelopment in -mediated retinal dysfunction. Ophthalmic Genetics. 40: 564-569. PMID 31900015 DOI: 10.1080/13816810.2019.1706749  0.314
2017 Ku CA, Hull S, Arno G, Vincent A, Carss K, Kayton R, Weeks D, Anderson GW, Geraets R, Parker C, Pearce DA, Michaelides M, MacLaren RE, Robson AG, Holder GE, et al. Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. Jama Ophthalmology. PMID 28542676 DOI: 10.1001/Jamaophthalmol.2017.1401  0.319
2016 Hull S, Mukherjee R, Holder GE, Moore AT, Webster AR. The clinical features of retinal disease due to a dominant mutation in RPE65. Molecular Vision. 22: 626-35. PMID 27307694  0.303
2015 Arno G, Hull S, Robson AG, Holder GE, Cheetham ME, Webster AR, Plagnol V, Moore AT. Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 56: 2358-65. PMID 25766589 DOI: 10.1167/Iovs.15-16520  0.317
2014 Hull S, Arno G, Plagnol V, Chamney S, Russell-Eggitt I, Thompson D, Ramsden SC, Black GC, Robson A, Holder GE, Moore AT, Webster AR. The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype. Investigative Ophthalmology & Visual Science. 55: 6934-44. PMID 25270190 DOI: 10.1167/Iovs.14-14715  0.319
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