Francis L. Munier

IC3D Classification of Corneal Dystrophies—Edition 2

Jayne S. Weiss, Hans Ulrik Møller, Anthony J. Aldave et al. · Cornea · 2015 · 510 citations · Full text

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

Edwin M. Stone, Andrew Lotery, Francis L. Munier et al. · Nature Genetics · 1999 · 491 citations

Ocular Disease, Retinal Dystrophy, Ophthalmology +8

Intravitreal chemotherapy for vitreous disease in retinoblastoma revisited: from prohibition to conditional indications

Francis L. Munier, Marie‐Claire Gaillard, Aubin Balmer et al. · British Journal of Ophthalmology · 2012 · 375 citations

Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis

Sylvain Hanein, Isabelle Perrault, S. Gerber et al. · Human Mutation · 2004 · 348 citations

Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2

Anren Li, Xiaodong Jiao, Francis L. Munier et al. · The American Journal of Human Genetics · 2004 · 280 citations · Full text

Mendelian Disorder, Ophthalmology, Corneal Dystrophy +6