Christian P. Hamel
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Mitochondrial Function and Pathology, Photoreceptor and optogenetics research, RNA regulation and disease
Most-Cited Works
- → The Retinal Pigment Epithelium in Health and Disease(2010)616 cited
- → Mutations in RPE65 cause Leber's congenital amaurosis(1997)608 cited
- → Dominant optic atrophy(2012)280 cited
- → OPA1 (Kjer Type) Dominant Optic Atrophy: A Novel Mitochondrial Disease(2002)188 cited
- → Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations(2009)164 cited
- → The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene(2018)129 cited
- → BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome(2012)125 cited
- → Bardet-Biedl Syndrome(2010)125 cited
- → Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission(2017)121 cited
- → A developmentally regulated microsomal protein specific for the pigment epithelium of the vertebrate retina(1993)118 cited