Carla Sanjurjo-Soriano

Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles

Carla Sanjurjo-Soriano, Nejla Erkilic, David Baux et al. · Molecular Therapy — Methods & Clinical Development · 2019 · 78 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3

Michalitsa Diakatou, Grégor Dubois, Nejla Erkilic et al. · International Journal of Molecular Sciences · 2021 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Retinoic acid delays initial photoreceptor differentiation and results in a highly structured mature retinal organoid

Carla Sanjurjo-Soriano, Nejla Erkilic, Krishna Damodar et al. · Stem Cell Research & Therapy · 2022 · 35 citations · Full text

Life Sciences, Developmental Biology, Vision Science +17

USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids

Carla Sanjurjo-Soriano, Carla Jimenez-Medina, Nejla Erkilic et al. · Human Genetics and Genomics Advances · 2023 · 20 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa

Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manès et al. · Stem Cell Research · 2018 · 11 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15