Bernard Arnaud

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

Cécile Delettre, Guy Lenaers, Jean‐Michel Griffoin et al. · Nature Genetics · 2000 · 1.4K citations

Neurodegenerative Diseases, Mitochondrial Function, Ophthalmology +9

Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindness

Thaddeus P. Dryja, Lauri B. Hahn, Thierry Reboul et al. · Nature Genetics · 1996 · 193 citations

Biology, α Subunit, Ophthalmology +5

Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa

Corinne Bareil, Christian Hamel, Valérie Delague et al. · Human Genetics · 2001 · 121 citations

Photoreceptor Cell, Molecular Neuroscience, Retina +6

Keratectasia Induced by Laser in situ Keratomileusis in Keratoconus

Clair‐Florent Schmitt‐Bernard, Cécile Lesage, Bernard Arnaud · Journal of Refractive Surgery · 2000 · 104 citations

Extensive Macular Atrophy with Pseudodrusen-like Appearance: A New Clinical Entity

Christian P. Hamel, Isabelle Meunier, Carl Arndt et al. · American Journal of Ophthalmology · 2009 · 69 citations

Ocular Disease, Ophthalmology, Extensive Macular Atrophy +4