Ridge-Adjacent Laser With Imaging and Dexamethasone for Treatment of Retinopathy of Prematurity
Hanna Maria Öhnell, Sandra Nobaek, Sten Andréasson, Lotta Gränse
0 citationsJournal of Pediatric Ophthalmology & Strabismus
Sten Andréasson
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253Publications signalées
6719Citations signalées
2Affiliations récentes
Institutions déclarées
Domaines associés
Retinal Development and DisordersRetinal Diseases and TreatmentsRetinal and Macular SurgeryGlaucoma and retinal disordersRetinopathy of Prematurity Studies
Publications récentes
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska et autres
14 citationsNature Genetics
Treating Retinopathy of Prematurity with Dexamethasone Eye Drops
Lotta Gränse, Hanna Maria Öhnell, Gerd Holmström, Johanna C Sundgren et autres
4 citationsOphthalmology
Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy
Karolina Kamińska, Francesca Cancellieri, Mathieu Quinodoz, Abigail R. Moye et autres
4 citationsThe American Journal of Human Genetics
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska et autres
15 citationsmedRxiv
Novel genetic cause of specific macular dystrophy due to biallelic variants in three genes encoding subunits of the AP-5 complex
Karolina Kamińska, Francesca Cancellieri, Mathieu Quinodoz, Abigail R. Moye et autres
0 citationsGhent University Academic Bibliography (Ghent University)
Lysosomal macular dystrophy is a novel ocular phenotype associated with biallelic variants affecting AP-5/ SPG11/SPG15 complex
Cristina Moreira Santos, Karolina Kaminska, Maximilian Pfau, Laura Kuehlewein et autres
0 citationsGhent University Academic Bibliography (Ghent University)
Variants in three genes encoding distinct subunits of the vesicular AP-5 complex are novel causes of recessive macular dystrophy
Karolina Kamińska, Francesca Cancellieri, Mathieu Quinodoz, Abigail R. Moye et autres
0 citationsGhent University Academic Bibliography (Ghent University)
A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing
Maria Areblom, Sten Kjellström, Sten Andréasson, Anders Öhberg et autres
9 citationsGenes
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis
Daan M. Panneman, Rebekkah J. Hitti‐Malin, Lara K. Holtes, Suzanne E. de Bruijn et autres
29 citationsFrontiers in Cell and Developmental Biology
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis
Daan M. Panneman, Rebekkah J. Hitti‐Malin, Lara K. Holtes, Suzanne E. de Bruijn et autres
2 citationsmedRxiv
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy
Bernd Wissinger, Britta Baumann, Elena Buena‐Atienza, Zeinab Ravesh et autres
14 citationsProceedings of the National Academy of Sciences
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