Ayberk Türkyılmaz

Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency

Erdal Kurnaz, Emine Kartal Baykan, Ayberk Türkyılmaz et al. · Hormone Research in Paediatrics · 2020 · 40 citations

Secondary findings in 622 Turkish clinical exome sequencing data

Esra Arslan Ateş, Ayberk Türkyılmaz, Özlem Yıldırım et al. · Journal of Human Genetics · 2021 · 17 citations

Medicine, Genetics, Next-generation Sequencing +4

Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency

Ayberk Türkyılmaz, Ceren Alavanda, Esra Arslan Ateş et al. · Journal of Assisted Reproduction and Genetics · 2022 · 14 citations · Full text

Infertility, Mendelian Disorder, Premature Ovarian Insufficiency +11

Chanarin-Dorfman syndrome

Semih Kalyon, Yasemin Gökden, Naciye Demirel et al. · The Turkish Journal of Gastroenterology · 2018 · 13 citations · Full text

Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey

Emine Kartal Baykan, Ayberk Türkyılmaz · Journal of Clinical Research in Pediatric Endocrinology · 2021 · 13 citations · Full text