Rubén Cabanillas

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

Xosé S. Puente, Vı́ctor Quesada, Fernando G. Osorio et al. · The American Journal of Human Genetics · 2011 · 210 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Néstor–Guillermo progeria syndrome: A novel premature aging condition with early onset and chronic development caused by <i>BANF1</i> mutations

Rubén Cabanillas, Juan Cadiñanos, José A.F. Villameytide et al. · American Journal of Medical Genetics Part A · 2011 · 154 citations · Full text

Medicine, Pediatrics, Genodermatoses +8

Oncologic outcomes of transoral laser surgery of supraglottic carcinoma compared with a transcervical approach

Rubén Cabanillas, Juan P. Rodrigo, José Luís Llorente et al. · Head & Neck · 2008 · 113 citations · Full text

Medicine, Oncology, Surgery +15

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

Rubén Cabanillas, Marta Diñeiro, Guadalupe Cifuentes et al. · BMC Medical Genomics · 2018 · 102 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Cell–cell adhesion genes CTNNA2 and CTNNA3 are tumour suppressors frequently mutated in laryngeal carcinomas

Miriam Fanjul‐Fernández, Vı́ctor Quesada, Rubén Cabanillas et al. · Nature Communications · 2013 · 91 citations · Full text

Medicine, Molecular Genetics, Oncology +13