Seda Taşır Yılmaz

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 · 112 citations · Full text

Medicine, Genetics, Otolaryngology +16

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

Aslı Sırmacı, Duygu Duman, Hatice Akay et al. · International Journal of Pediatric Otorhinolaryngology · 2009 · 61 citations

Life Sciences, Genetics, Molecular Genetics +11

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

Ali Kemal Oğuz, Seda Taşır Yılmaz, Çağdaş Şahap Oygür et al. · PLoS ONE · 2016 · 22 citations · Full text

Life Sciences, Bioinformatics, Immunology +16

C-type lectin domain family 12, member A: A common denominator in Behçet’s syndrome and acute gouty arthritis

Ali Kemal Oğuz, Seda Taşır Yılmaz, Nejat Akar et al. · Medical Hypotheses · 2015 · 11 citations

Life Sciences, Immunology, Pathology +10