Miguel Carballo

Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Irene Perea‐Romero, Gema Gordo, Ionut-Florin Iancu et al. · Scientific Reports · 2021 · 160 citations · Full text

Life Sciences, Genetics, Ophthalmology +16

Mutations in the Pre-mRNA Splicing-Factor Genes<i>PRPF3</i>,<i>PRPF8</i>, and<i>PRPF31</i>in Spanish Families with Autosomal Dominant Retinitis Pigmentosa

Mari ́a Marti ́nez-Gimeno, Mari ́a Jose ́ Gamundi, Imma Hernán et al. · Investigative Ophthalmology & Visual Science · 2003 · 98 citations

Life Sciences, Genetics, Ophthalmology +15

Clinical pharmacogenomic testing of KRAS, BRAF and EGFRmutations by high resolution melting analysis and ultra-deep pyrosequencing

Emma Borràs, Ismael Jurado, Imma Hernán et al. · BMC Cancer · 2011 · 92 citations · Full text

Medicine, Molecular Genetics, Oncology +17

DNA and histone H1 interact with different domains of HMG 1 and 2 proteins.

Miguel Carballo, Pere Puigdomènech, Jaume Palau · The EMBO Journal · 1983 · 84 citations · Full text

Life Sciences, Genetics, Molecular Biology +12

Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II

Elena Aller, Teresa Jaijo, Magdalena Beneyto et al. · Journal of Medical Genetics · 2006 · 79 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12