Josephine Prener Holtan
6PUBLICATIONS
164CO-AUTHORS
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Publications (6)
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|Feb 02, 2026
Clinical and genetic characterization of BEST1-associated retinal dystrophies in the Norwegian population.Erlend Sæther, Geir Bertelsen, Ragnheidur Bragadottir
|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova
|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova
|Dec 01, 2020
Clinical features and molecular genetics of patients with ABCA4-retinal dystrophies.Josephine Prener Holtan, Ingvild Aukrust, Ragnhild Wivestad Jansson
|Aug 21, 2019
Inherited retinal disease in Norway - a characterization of current clinical and genetic knowledge.Josephine Prener Holtan, Kaja Kristine Selmer, Ketil Riddervold Heimdal
|Apr 02, 2019
Dominant ARL3-related retinitis pigmentosa.Josephine Prener Holtan, Knut Teigen, Ingvild Aukrust
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Frequent Collaborators
2 joint publications
Beatrice Bocquet
2 joint publications
Kim Rodenburg
2 joint publications
Carmen Ayuso
2 joint publications
Suzanne E de Bruijn
2 joint publications
David G Birch
2 joint publications
Manir Ali
2 joint publications
Mirella T S Barboni
2 joint publications
Sandro Banfi
2 joint publications
K Bailey Freund
2 joint publications
Lara K Holtes
