Rosario Paredes

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Güney Bademci, Joseph Foster, Nejat Mahdieh et al. · Genetics in Medicine · 2015 · 159 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations

Güney Bademci, Akeem O. Lasisi, Kemal O. Yariz et al. · BMC Medical Genetics · 2015 · 27 citations · Full text

Life Sciences, Audiology, Genetics +12

Novel EYA1 variants causing Branchio-oto-renal syndrome

Kyle D. Klingbeil, Christopher M. Greenland, Selçuk Arslan et al. · International Journal of Pediatric Otorhinolaryngology · 2017 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Association between the APOE<i>ε</i>4 Allele and Late-Onset Alzheimer’s Disease in an Ecuadorian Mestizo Population

Stefany Montufar-Armendariz, Cristian Calero, Rodrigo Vinueza et al. · International Journal of Alzheimer s Disease · 2017 · 21 citations · Full text

Life Sciences, Genetics, Neurology +17