Silvia Modamio‐Høybjør
Hospital Universitario La Paz(ES)Instituto de Salud Carlos III(ES)Hospital La Paz Institute for Health Research(ES)Centre for Biomedical Network Research on Rare Diseases(ES)Centro de Investigación Biomédica en Red(ES)ERN GUARD-Heart(NL)Universidad Autónoma de Madrid(ES)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Connective tissue disorders research, Vestibular and auditory disorders, Ubiquitin and proteasome pathways, RNA modifications and cancer
Most-Cited Works
- → Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss(2009)551 cited
- → Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing(2019)105 cited
- → DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss(2011)92 cited
- → In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment(2009)77 cited
- → A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor–Mediated Cell Signaling, Causes Progressive Hearing Loss(2007)75 cited
- → Differential Biological Role of CD3 Chains Revealed by Human Immunodeficiencies(2007)74 cited