Françoise Meire

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Maria M. van Genderen, Mieke M. C. Bijveld, Y. Claassen et al. · The American Journal of Human Genetics · 2009 · 245 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation

Diane Beysen, Christine Oley, Birgit Lorenz et al. · The American Journal of Human Genetics · 2003 · 243 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Low vision affects dynamic stability of gait

Ann Hallemans, Els Ortibus, Françoise Meire et al. · Gait & Posture · 2010 · 213 citations

Education, Robotics Engineering, Vision Science +12

A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

Susanne Kohl, Frauke Coppieters, Françoise Meire et al. · The American Journal of Human Genetics · 2012 · 184 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

Borate transporter <i>SLC4A11</i> mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

Julie Désir, Graciela Moya, Orit Reish et al. · Journal of Medical Genetics · 2007 · 165 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15