| Cochlear implant–state of the art T Lenarz Laryngo-rhino-otologie 96 (S 01), S123-S151, 2017 | 362 | 2017 |
| OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation R Santarelli, R Rossi, P Scimemi, E Cama, ML Valentino, C La Morgia, ... Brain 138 (3), 563-576, 2015 | 105 | 2015 |
| BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice G Crispino, G Di Pasquale, P Scimemi, L Rodriguez, F Galindo Ramirez, ... PloS one 6 (8), e23279, 2011 | 79 | 2011 |
| The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice M Schuetz, P Scimemi, P Majumder, RD De Siati, G Crispino, L Rodriguez, ... Human molecular genetics 19 (24), 4759-4773, 2010 | 79 | 2010 |
| Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene R Santarelli, I Del Castillo, M Rodríguez-Ballesteros, P Scimemi, E Cama, ... Journal of the Association for Research in Otolaryngology 10, 545-556, 2009 | 75 | 2009 |
| Cochlear microphonic potential recorded by transtympanic electrocochleography in normally-hearing and hearing-impaired ears R Santarelli, P Scimemi, E Dal Monte, E Arslan Acta otorhinolaryngologica italica 26 (2), 78, 2006 | 72 | 2006 |
| The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice M Bortolozzi, M Brini, N Parkinson, G Crispino, P Scimemi, RD De Siati, ... Journal of Biological Chemistry 285 (48), 37693-37703, 2010 | 71 | 2010 |
| Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations R Santarelli, I del Castillo, E Cama, P Scimemi, A Starr Hearing research 330, 200-212, 2015 | 59 | 2015 |
| Reduced phosphatidylinositol 4, 5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition L Rodriguez, E Simeonato, P Scimemi, F Anselmi, B Calì, G Crispino, ... Proceedings of the National Academy of Sciences 109 (35), 14013-14018, 2012 | 51 | 2012 |
| Auditory brainstem responses to clicks and tone bursts in C57 BL/6J mice P Scimemi, R Santarelli, A Selmo, F Mammano Acta Otorhinolaryngologica Italica 34 (4), 264, 2014 | 44 | 2014 |
| Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions R Santarelli, E Cama, P Scimemi, E Dal Monte, E Genovese, E Arslan European archives of oto-rhino-laryngology 265, 43-51, 2008 | 39 | 2008 |
| Auditory neuropathy in systemic sclerosis: a speech perception and evoked potential study before and after cochlear implantation R Santarelli, P Scimemi, E Dal Monte, E Genovese, E Arslan European Archives of Oto-Rhino-Laryngology and Head & Neck 263, 809-815, 2006 | 36 | 2006 |
| Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction PJ Kullar, J Quail, P Lindsey, JA Wilson, R Horvath, P Yu-Wai-Man, ... Brain 139 (6), e33-e33, 2016 | 20 | 2016 |
| A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members F Cesca, E Bettella, R Polli, E Cama, P Scimemi, R Santarelli, A Murgia International Journal of Pediatric Otorhinolaryngology 104, 88-93, 2018 | 16 | 2018 |
| Presynaptic and postsynaptic mechanisms underlying auditory neuropathy in patients with mutations in the OTOF or OPA1 gene R Santarelli, A Starr, I Del Castillo, T Huang, P Scimemi, E Cama, R Rossi, ... Audiological Medicine 9 (2), 59-66, 2011 | 14 | 2011 |
| Cochlear synaptopathy due to mutations in OTOF gene may result in stable mild hearing loss and severe impairment of speech perception R Santarelli, P Scimemi, M Costantini, M Domínguez-Ruiz, ... Ear and Hearing 42 (6), 1627-1639, 2021 | 13 | 2021 |
| Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory … M Domínguez-Ruiz, M Rodríguez-Ballesteros, M Gandía, E Gómez-Rosas, ... Genes 13 (1), 149, 2022 | 10 | 2022 |
| Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype F Cesca, E Bettella, R Polli, E Leonardi, MC Aspromonte, B Sicilian, ... Journal of Human Genetics 65 (10), 855-864, 2020 | 10 | 2020 |
| Cochlear implantation in children with Autism Spectrum Disorder (ASD): Outcomes and implant fitting characteristics P Mancini, L Mariani, M Nicastri, S Cavicchiolo, I Giallini, P Scimemi, ... International Journal of Pediatric Otorhinolaryngology 149, 110876, 2021 | 8 | 2021 |
| Abnormal cochlear potentials in Friedreich's ataxia point to disordered synchrony of auditory nerve fiber activity R Santarelli, E Cama, E Pegoraro, P Scimemi Neurodegenerative Diseases 15 (2), 114-120, 2015 | 8 | 2015 |
