Saba Battelino

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Crystel Bonnet, Zied Riahi, Sandra Chantot‐Bastaraud et al. · European Journal of Human Genetics · 2016 · 106 citations · Full text

Structural alterations of brain grey and white matter in early deaf adults

Manja Hribar, Dušan Šuput, Altiere Araujo Carvalho et al. · Hearing Research · 2014 · 62 citations · Full text

Neuropsychology, White Matter, Neurolinguistics +22

The possible influence of genetic aetiological factors on molar–incisor hypomineralisation

Luka Hočevar, Jernej Kovač, Katarina Trebušak Podkrajšek et al. · Archives of Oral Biology · 2020 · 37 citations · Full text

Change of Phonation Control After Cochlear Implantation

Irena Hočevar Boltežar, Z Radsel, Jagoda Vatovec et al. · Otology & Neurotology · 2006 · 35 citations

Hearing Health, Adult Audiology, Voice Quality +22

TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss

Saba Battelino, Gašper Klančar, Jernej Kovač et al. · European Archives of Oto-Rhino-Laryngology · 2015 · 32 citations

Audiology, Tmprss3 Mutations, Auditory Research +5