Filiz Başak Cengiz

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

Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Oscar Diaz‐Horta, Duygu Duman, Joseph Foster et al. · PLoS ONE · 2012 · 155 citations · Full text

Genetics, Pathology, Arnshl Genes +16

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

Denise Yan, Demet Tekin, Güney Bademci et al. · Human Genetics · 2016 · 136 citations · Full text

Allelic Variant, Multiple Continents, Mendelian Disorder +12

Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

Mustafa Tekin, Burcu Öztürk Hişmi, Suat Fítöz et al. · The American Journal of Human Genetics · 2007 · 111 citations · Full text

Homozygous Mutations, Developmental Biology, Syndromic Deafness Characterized +10

Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey

Duygu Duman, Filiz Başak Cengiz, Hi̇lal Özdağ et al. · Genetic Testing and Molecular Biomarkers · 2010 · 90 citations

Nonsyndromic Deafness, Mendelian Disorder, Genetic Disorder +13