Magdalena Beneyto

Hospital Clínico Universitario de Valencia — Spain

Neuroscience · Life Sciences

21h-index1.4kcitations67works0.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Hearing, Cochlea, Tinnitus, Genetics(17), Retinal Development and Disorders(12), RNA and protein synthesis mechanisms(4), Vestibular and auditory disorders(4), Cancer-related Molecular Pathways(4)

Publications67 total

Management of Thyroid Gland Abscess
Acta Otorrinolaringologica (English Edition)·2019· 4 cited
Manejo del absceso de la glándula tiroides
Acta Otorrinolaringológica Española·2018· 1 cited
Hiccups. Attitude in Otorhinolaryngology Towards Consulting Patients. A Diagnostic and Therapeutic Approach
Acta Otorrinolaringologica (English Edition)·2017· 3 cited
Hipo. Actitud en otorrinolaringología en pacientes que consultan. Aproximación diagnóstica y terapéutica
Acta Otorrinolaringológica Española·2016· 2 cited
Factors Related to Post-tonsillectomy Pain in Adults
Acta Otorrinolaringologica (English Edition)·2016· 6 cited
Factores relacionados al dolor postamigdalectomía en adultos
Acta Otorrinolaringológica Española·2015· 4 cited
Malformación de Arnold-Chiari en el síndrome de Noonan y otros síndromes de la vía RAS/MAPK
Revista de Neurología·2015· 15 cited
Tratamiento quirúrgico de los trastornos respiratorios del sueño en la infancia
Revista española de ortodoncia·2012
SRD5A2 gene mutations and polymorphisms in Spanish 46,XY patients with a disorder of sex differentiation
International Journal of Andrology·2011· 39 citedOpen Access
Familial multiple cavernomatosis: Description of a new mutation
Neurología (English Edition)·2011· 2 cited
Cavernomatosis múltiple familiar: descripción de una nueva mutación
Neurología·2010· 4 cited
Microarray-Based Mutation Analysis of 183 Spanish Families with Usher Syndrome
Investigative Ophthalmology & Visual Science·2010· 63 cited
Novel (60%) and Recurrent (40%) Androgen Receptor Gene Mutations in a Series of 59 Patients with a 46,XY Disorder of Sex Development
The Journal of Clinical Endocrinology & Metabolism·2010· 145 citedOpen Access
El asesoramiento genético en los déficits visuales y auditivos
Archivos de la Sociedad Española de Oftalmología·2008· 4 citedOpen Access
Severe and moderate hemophilia A: identification of 38 new genetic alterations
Haematologica·2008· 25 citedOpen Access
<i>MYO7A</i> mutation screening in Usher syndrome type I patients from diverse origins
Journal of Medical Genetics·2007· 70 citedOpen Access
Screening of the<i>USH1G</i>Gene among Spanish Patients with Usher Syndrome. Lack of Mutations and Evidence of a Minor Role in the Pathogenesis of the Syndrome
Ophthalmic Genetics·2007· 11 cited
Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II
Journal of Medical Genetics·2006· 79 citedOpen Access
Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma
Human Mutation·2006· 44 cited
Retinoblastoma: implicaciones del estudio genético-molecular
Medicina Clínica·2006
page 1 of 4Next →

Frequent Co-authors

Carmén Nájera(19), José M. Millán(13), Carmen Ayuso(12), Elena Aller(9), Félix Prieto(9), Montserrat Baiget(8), Francisco Javier García Callejo(8), Teresa Jaijo(7), Herminio Pérez-Garrigues(7), Carmen Espinós(6), Guillermo Antiñolo(5), Silvestre Oltra(5), C Vilela(5), Francisco Sánchez‐Sánchez(5), Diana Valverde(4), Francesc Palau(4), Lourdes Badı́a(4), Inés Rincón Piedrahita(4), Rafael Monzó Gandía(4), Jaume Redondo Martínez(4)