Bernard Arnaud
Universidade do Estado do Pará(BR)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Corneal surgery and disorders, Photoreceptor and optogenetics research, Glaucoma and retinal disorders
Most-Cited Works
- → Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy(2000)1,421 cited
- → Mutations in RPE65 cause Leber's congenital amaurosis(1997)608 cited
- → Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindness(1996)193 cited
- → Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa(2001)121 cited
- → Keratectasia Induced by Laser in situ Keratomileusis in Keratoconus(2000)104 cited
- → Extensive Macular Atrophy with Pseudodrusen-like Appearance: A New Clinical Entity(2009)70 cited
- → Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene(1998)62 cited
- → Screening Genes of the Retinoid Metabolism: Novel LRAT Mutation in Leber Congenital Amaurosis(2006)46 cited
- → Homozygous Deletion Related to Alu Repeats inRLBP1Causes Retinitis Punctata Albescens(2006)39 cited
- → In Vitro Creation of Amyloid Fibrils from Native and Arg124Cys Mutated βIGH3(110–131) Peptides, and Its Relevance for Lattice Corneal Amyloid Dystrophy Type I(2000)31 cited