Esra Arslan Ateş

A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

Esther Pohl, Ayça Aykut, Filippo Beleggia et al. · Human Genetics · 2013 · 60 citations

Mendelian Disorder, Genetic Disorder, Genetics +3

Relationship Between IL1β-511C>T and ILRN VNTR Polymorphisms and Keratoconus

Melis Palamar, Hüseyin Önay, Taha Reşid Özdemir et al. · Cornea · 2013 · 21 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

Genotype and Anterior Segment Phenotype in a Cohort of Turkish Patients with Lamellar Ichthyosis

Melis Palamar, Hüseyin Önay, İlgen Ertam et al. · Ophthalmic Genetics · 2014 · 14 citations

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