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Methods in Molecular Biology (Clifton, N.J.)|March 23, 2021
CRISPR/Cas9-Mediated Genome Editing to Generate Clonal iPSC LinesCarla Sanjurjo-Soriano, Nejla Erkilic, Daria Mamaeva, et al.
Stem Cell Research|June 27, 2026
Generation of an induced pluripotent stem cell line, LGMi002-A, from a Bardet-Biedl Syndrome patient with a BBS5 homozygous pathogenic variantSamira Secula, Nejla Erkilic, Cathy Obringer, et al.
International Journal of Molecular Sciences|April 3, 2021
Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3Michalitsa Diakatou, Gregor Dubois, Nejla Erkilic, et al.
Stem Cell Research|March 6, 2022
Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Christel Vache, et al.
Stem Cell Research|November 20, 2018
Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Stem Cell Research|November 24, 2018
Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Human Molecular Genetics|September 16, 2017
Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapySimona Torriano, Nejla Erkilic, Valérie Faugère, et al.
Stem Cell Research|June 28, 2019
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosisNejla Erkilic, Carla Sanjurjo-Soriano, Gaël Manes, et al.
Stem Cell Research|April 26, 2026
Generation of an induced pluripotent stem cell line from an Alström syndrome patient with biallelic ALMS1 pathogenic variantsSamira Secula, Nejla Erkilic, Cathy Obringer, et al.
Stem Cell Research|June 17, 2019
Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophyNejla Erkilic, Carla Sanjurjo-Soriano, Michalitsa Diakatou, et al.
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