Sally Hooghe

Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes

Frauke Coppieters, Ingele Casteels, Françoise Meire et al. · Human Mutation · 2010 · 146 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Expanding the Spectrum of<i>FOXC1</i>and<i>PITX2</i>Mutations and Copy Number Changes in Patients with Anterior Segment Malformations

Barbara D′haene, Françoise Meire, Ilse Claerhout et al. · Investigative Ophthalmology & Visual Science · 2010 · 91 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations

Kristof Van Schil, Sarah Naessens, Stijn Van de Sompele et al. · Genetics in Medicine · 2017 · 67 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus

Basamat Almoallem, Miriam Bauwens, Sophie Walraedt et al. · Investigative Ophthalmology & Visual Science · 2015 · 48 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16