Françoise Roulez

LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma

Julie Désir, Yves Sznajer, Fanny Depasse et al. · European Journal of Human Genetics · 2010 · 118 citations · Full text

Medicine, Genetics, Ophthalmology +17

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

Congenital Fixed Dilated Pupils Due to ACTA2– Multisystemic Smooth Muscle Dysfunction Syndrome

Françoise Roulez, Fran Faes, Patricia Delbeke et al. · Journal of Neuro-Ophthalmology · 2014 · 38 citations

Medicine, Cardiology, Ophthalmology +16

Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals <i>CYP1B1</i> and <i>FOXC1</i> Variants as Most Frequent Causes

Elena Lang, Samuel Koller, Luzy Bähr et al. · Translational Vision Science & Technology · 2020 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes.

Françoise Meire, Isabelle Delpierre, Cécile Brachet et al. · PubMed · 2011 · 21 citations · Full text

Medicine, Genetics, Ophthalmology +16