Listar por autor "Bademci, Guney"

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  • Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss. 
    Ramzan, Memoona; Duman, Duygu; Hendricks, LeShon Chere Peart; Guo, Shengru; Mutlu, Ahmet; Kalcioglu, Mahmut Tayyar; Seyhan, Serhat; Carranza, Claudia; Bonyadi, Murtaza; Mahdieh, Nejat; Yildirim-Baylan, Muzeyyen; Figueroa Ildefonso, Erick Gianpierre; Alper, Ozgul; Atik, Tahir; Ayral, Abdurrahman; Bozan, Nazim; Balta, Burhan; Rivas, Christian; Manzoli, Gabrielle N.; Huesca-Hernandez, Fabiola; Kuchay, Raja A. H.; Durgut, Merve; Bademci, Guney; Tekin, Mustafa (Springer, 2023)
    Hearing loss (HL) is a common heterogeneous trait that involves variants in more than 200 genes. In this study, we utilized exome (ES) and genome sequencing (GS) to effectively identify the genetic cause of presumably ...
  • Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population 
    Figueroa Ildefonso, Erick Gianpierre; Bademci, Guney; Rajabli, Farid; Cornejo-Olivas, Mario; Villanueva, Ruy Diego Chacon; Badillo-Carrillo, Rodolfo; Inca-Martinez, Miguel; Neyra, Karina Milla; Sineni, Claire; Tekin, Mustafa (MDPI, 2019)
    Hearing loss (HL) is a common sensory disorder affecting over 5% of the global population. The etiology underlying HL includes congenital and acquired causes; genetic factors are the main cause in over 50% of congenital ...

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