Concepedia
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Publications
11
Citations
1.5K
H-Index
Active since
2004
Affiliations
Radboud University Nijmegen(Current)
Radboud University Medical Center
Rotterdam Eye Hospital
Max Planck Institute for Molecular Genetics
Heidelberg University
Krysta Voesenek is an author at Radboud University Nijmegen specializing in genetics, molecular genetics, and genetic disorders.
Publications per year
2004–2014
Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
Anneke I. den Hollander, Robert K. Koenekoop, Suzanne Yzer et al. · The American Journal of Human Genetics · 2006 · 676 citations · Full text
Life Sciences, Genetics, Molecular Genetics +4
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
Heleen H. Arts, Dan Doherty, Sylvia E. C. van Beersum et al. · Nature Genetics · 2007 · 321 citations
Life Sciences, Genetics, Molecular Genetics +8
Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa
Dikla Bandah‐Rozenfeld, Rob W.J. Collin, Eyal Banin et al. · The American Journal of Human Genetics · 2010 · 106 citations · Full text
Medicine, Genetics, Molecular Genetics +13
Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis.
José A. J. M. van den Hurk, Penny Rashbass, Ronald Roepman et al. · PubMed · 2005 · 92 citations
Medicine, Genetics, Molecular Genetics +8
Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis
Suzanne Yzer, Bart P. Leroy, Thomy de Ravel et al. · Investigative Ophthalmology & Visual Science · 2006 · 92 citations · Full text
Life Sciences, Genetics, Molecular Genetics +17
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