Josseline Kaplan
Inserm(FR)Université Paris Cité(FR)Sorbonne Université(FR)Sorbonne Paris Cité(FR)Westinghouse Electric (Germany)(DE)Westinghouse Electric (Japan)(JP)Institut des Maladies Génétiques Imagine(FR)Westinghouse Electric (United States)(US)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Mitochondrial Function and Pathology, RNA regulation and disease, Glaucoma and retinal disorders
Most-Cited Works
- → Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy(2000)1,421 cited
- → Defective myosin VIIA gene responsible for Usher syndrome type IB(1995)1,065 cited
- → Illegitimate transcription: transcription of any gene in any cell type.(1989)638 cited
- → International Committee for Standardization in Haematology: Recommended Methods for Red‐Cell Enzyme Analysis*(1977)540 cited
- → Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis(1996)445 cited
- → Mutation spectrum and splicing variants in the OPA1 gene(2001)379 cited