Renate C. Zekveld-Vroon

Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders

Alberta A. H. J. Thiadens, Anneke I. den Hollander, Susanne Roosing et al. · The American Journal of Human Genetics · 2009 · 215 citations · Full text

Medicine, Molecular Genetics, Neuroscience +13

Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone–Rod Dystrophy

Alberta A. H. J. Thiadens, T. My Lan Phan, Renate C. Zekveld-Vroon et al. · Ophthalmology · 2012 · 137 citations

Medicine, Genetics, Ophthalmology +13

LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS

Inge B. Mathijssen, Ralph J. Florijn, L. Ingeborgh van den Born et al. · Retina · 2016 · 41 citations · Full text

Medicine, Genetics, Ophthalmology +17

Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype

Isabelle Perrault, Alejandro Estrada‐Cuzcano, Irma López et al. · PLoS ONE · 2013 · 21 citations · Full text

Medicine, Genetics, Molecular Genetics +12

After the Introduction into the National Newborn Screening Program: Who Is Receiving Genetic Counseling for Hemoglobinopathies in The Netherlands?

Judith O. Kaufmann, Ingrid P.C. Krapels, Bernadette T J van Brussel et al. · Public Health Genomics · 2013 · 12 citations

Medicine, Genetics, Pediatrics +17