| Targeted next generation sequencing for molecular diagnosis of Usher syndrome MJ Aparisi, E Aller, C Fuster-García, G García-García, R Rodrigo, ... Orphanet journal of rare diseases 9, 1-15, 2014 | 102 | 2014 |
| USH2A gene editing using the CRISPR system C Fuster-García, G García-García, E González-Romero, T Jaijo, ... Molecular Therapy-Nucleic Acids 8, 529-541, 2017 | 72 | 2017 |
| Usher syndrome: genetics of a human ciliopathy C Fuster-García, B García-Bohórquez, A Rodríguez-Muñoz, E Aller, ... International journal of molecular sciences 22 (13), 6723, 2021 | 57 | 2021 |
| High-throughput sequencing for the molecular diagnosis of Usher syndrome reveals 42 novel mutations and consolidates CEP250 as Usher-like disease causative C Fuster-García, G García-García, T Jaijo, N Fornés, C Ayuso, ... Scientific Reports 8 (1), 17113, 2018 | 37 | 2018 |
| Genotype–phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials L Galbis‐Martínez, F Blanco‐Kelly, G García‐García, A Ávila‐Fernández, ... Acta Ophthalmologica 99 (8), 922-930, 2021 | 11 | 2021 |
| Expanding the genetic landscape of usher-like phenotypes C Fuster-Garcia, G Garcia-Garcia, T Jaijo, F Blanco-Kelly, L Tian, ... Investigative Ophthalmology & Visual Science 60 (14), 4701-4710, 2019 | 9 | 2019 |
| Generation of the first human in vitro model for McArdle disease based on iPSC technology MC Ortuño-Costela, V Cerrada, A Moreno-Izquierdo, I García-Consuegra, ... International Journal of Molecular Sciences 23 (22), 13964, 2022 | 7 | 2022 |
| Application of CRISPR tools for variant interpretation and disease modeling in inherited retinal dystrophies C Fuster-García, B García-Bohórquez, A Rodríguez-Muñoz, JM Millán, ... Genes 11 (5), 473, 2020 | 7 | 2020 |
| Genetic screening of the usher syndrome in Cuba EE Santana, C Fuster-García, E Aller, T Jaijo, B García-Bohórquez, ... Frontiers in genetics 10, 501, 2019 | 7 | 2019 |
| Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment G García-García, I Sanchez-Navarro, E Aller, T Jaijo, C Fuster-Garcia, ... Molecular Vision 26, 216, 2020 | 5 | 2020 |
| Integration of ζ-deficient CARs into the CD3ζ gene conveys potent cytotoxicity in T and NK cells J Kath, C Franke, V Drosdek, W Du, V Glaser, C Fuster-Garcia, M Stein, ... Blood 143 (25), 2599-2611, 2024 | 4 | 2024 |
| Therapeutic approaches and development of genomic diagnostic tools for Usher syndrome C Fuster García Universitat Politècnica de València, 2020 | 2 | 2020 |
| Generating universal anti-CD19 CAR T cells with a defined memory phenotype by CRISPR/Cas9 editing and safety evaluation of the transcriptome K Pavlovic, MD Carmona-Luque, GI Corsi, N Maldonado-Pérez, ... Frontiers in Immunology 15, 1401683, 2024 | 1 | 2024 |
| Gene editing of CD3 epsilon gene to redirect regulatory T cells for adoptive T cell transfer W Du, F Noyan, O McCallion, V Drosdek, J Kath, V Glaser, ... bioRxiv, 2024.03. 18.584896, 2024 | | 2024 |
| Repair of the prevalent c. 2299delG mutation in the USH2A gene using CRISPR/Cas9 nucleases C Fuster-Garcia, G Garcia-Garcia, E Gonzalez-Romero, T Jaijo, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 195-195, 2018 | | 2018 |
| USH2A gene editing by CRISPR/Cas9 system C Fuster-Garcia, E Gonzalez-Romero, G Garcia-Garcia, T Jaijo, ... HUMAN GENE THERAPY 27 (11), A142-A143, 2016 | | 2016 |
