François‐Xavier Borruat

Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness

Christina Zeitz, Barbara Kloeckener‐Gruissem, U. Förster et al. · The American Journal of Human Genetics · 2006 · 179 citations · Full text

Ocular Disease, Signal Transduction, Retina +9

The<i>PROM1</i>Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

Michel Michaelides, Marie‐Claire Gaillard, Pascal Escher et al. · Investigative Ophthalmology & Visual Science · 2010 · 121 citations · Full text

Face recognition and postero-inferior hemispheric lesions

Stéphanie Clarke, Astrigh Lindemann, Philippe Maeder et al. · Neuropsychologia · 1997 · 104 citations

Face Detection, Facial Recognition System, Face Recognition +3

An unusual presentation of herpes zoster ophthalmicus: orbital myositis preceding vesicular eruption

Aki Kawasaki, François‐Xavier Borruat · American Journal of Ophthalmology · 2003 · 63 citations

Unusual Presentation, Orbital Myositis, Ophthalmology +4

Patterns of Rod and Cone Dysfunction in Bardet-Biedl Syndrome

Samuel G. Jacobson, François‐Xavier Borruat, Peter P. Apáthy · American Journal of Ophthalmology · 1990 · 53 citations · Full text