Raymon Vijzelaar

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 3

Top Topics

Mitochondrial Dna

Diabetic Retinopathy

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Neurology. Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Bernd Wissinger, Britta Baumann, Elena Buena-Atienza, Zeinab Ravesh, Artur V Cideciyan, Katarina Stingl, Isabelle Audo, Isabelle Meunier, Béatrice Bocquet, Elias I Traboulsi, Alison J Hardcastle, Jessica C Gardner, Michel Michaelides, Kari E Branham, Thomas Rosenberg, Sten Andreasson, Hélène Dollfus, David Birch, Andrea L Vincent, Loreto Martorell, Jaume Catala, Ulrich Kellner, Klaus Rüther, Birgit Lorenz, Markus N Preising, Emanuela Manfredini, Yuri A Zarate, Raymon Vijzelaar, Eberhart Zrenner, Samuel G Jacobson, Susanne Kohl
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy. Proceedings of the National Academy of Sciences of the United States of America 119 (27) (2022)
Jeroen W Bos, Ewout Joan Nicolaas Groen, Renske I Wadman, Chantall A D Curial, Naomi N Molleman, Marinka Zegers, Paul W J van Vught, Reinier Snetselaar, Raymon Vijzelaar, W Ludo van der Pol, Leonard H van den Berg
SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis. Neurology. Genetics 7 (4) (2021)
Raymon Vijzelaar, Reinier Snetselaar, Martijn Clausen, Amanda G Mason, Marrit Rinsma, Marinka Zegers, Naomi Molleman, Renske Boschloo, Rizkat Yilmaz, Romy Kuilboer, Sylvia Lens, Syamiroh Sulchan, Jan Schouten
The frequency of SMN gene variants lacking exon 7 and 8 is highly population dependent. PloS one 14 (7) (2019)