Güney Bademci

Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia

Michail Spiliopoulos, Francesco Brancati, Eric Powell et al. · The American Journal of Human Genetics · 2011 · 256 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

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

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

Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform

Dale J. Hedges, Toumy Guettouche, Shan Yang et al. · PLoS ONE · 2011 · 93 citations · Full text

Engineering, Genetics, Molecular Biology +21

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing

Oscar Diaz‐Horta, Asli Subasioglu-Uzak, M’hamed Grati et al. · Proceedings of the National Academy of Sciences · 2014 · 79 citations · Full text