Armağan İncesulu

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 551 citations · Full text

Genetic Disorder, Genetics, Audiology +9

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 · 158 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +11

Children With Cochlear Implants: Parental Perspective

Armağan İncesulu, M. Vural, Ünsal Erkam · Otology & Neurotology · 2003 · 135 citations

Correlation of Acoustic Threshold Measures and Spiral Ganglion Cell Survival in Severe to Profound Sensorineural Hearing Loss: Implications for Cochlear Implantation

Armağan İncesulu, Joseph B. Nadol · Annals of Otology Rhinology & Laryngology · 1998 · 110 citations

Hearing Health, Temporal Bone Study, Social Sciences +17

Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey

Mustafa Tekin, Türker Duman, G Boğoçlu et al. · European Journal of Pediatrics · 2003 · 65 citations

Genetic Testing, Mtdna A1555g, Genetic Disorder +8