Fernando Mayo

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss

Ángeles Mencía, Silvia Modamio‐Høybjør, Nick Redshaw et al. · Nature Genetics · 2009 · 548 citations

Developmental Biology, Genetics, Audiology +9

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss

Michael S. Hildebrand, Matías Morin, Nicole C. Meyer et al. · Human Mutation · 2011 · 92 citations · Full text

Genetics, Genetic Epidemiology, Pathology +26

Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants

Matías Morin, Lucía Borreguero, Kevin T. Booth et al. · Scientific Reports · 2020 · 84 citations · Full text

In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment

Matías Morin, Keith E. Bryan, Fernando Mayo et al. · Human Molecular Genetics · 2009 · 77 citations · Full text

Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane

P. Kevin Legan, Richard J. Goodyear, Matías Morin et al. · Human Molecular Genetics · 2013 · 56 citations · Full text

Genetics, Molecular Genetics, Different Tecta +24