Concepedia

Fernando Mayo

FM

Statistics

Publications

5

Citations

867

H-Index

5

Active since

2009

Affiliations

Centre for Biomedical Network Research on Rare Diseases(Current)

Instituto Cajal

Instituto Ramón y Cajal de Investigación Sanitaria

Hospital Universitario Ramón y Cajal

University of Iowa

Fernando Mayo is an author at Centre for Biomedical Network Research on Rare Diseases specializing in life sciences, cochlear disorders, and hearing loss.

ORCID

Publications per year

2009–2020

5

Publications

5

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 · 555 citations

, , +14

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 · 93 citations · Full text

, , +12

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 · 85 citations · Full text

, , +17

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

, , +13

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 · 57 citations · Full text

, , +17

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