Concepedia

Françoise Meire

FM

Statistics

Publications

65

Citations

4.1K

H-Index

39

Active since

1985

Affiliations

Ghent University Hospital(Current)

Queen Fabiola Children's University Hospital

KU Leuven

Erasmus Hospital

Inserm

Françoise Meire is an author at Ghent University Hospital specializing in genetics, human genetics, and medical genetics.

Publications per year

1985–2019

65

Publications

65

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

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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

, , +14

Low vision affects dynamic stability of gait

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

, , +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

, , +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

, , +15

1–5 of 65