E. Ataman

The Investigation of English Teachers’ Views on Computer Assisted Language Learning

E. Ataman, 2020, The Universal Academic Research Journal.

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

M. Baumgartner, A. Kariminejad, C. Marcelis, 2011, Orphanet journal of rare diseases.

Relationship between plasminogen activator inhibitor‐1 gene alterations and fibrosis in peritoneal dialysis patients

E. Ataman, M. Tanrisev, S. Ersan, 2020, Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy.

Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy

P. Gencpinar, E. Ataman, U. Yiş, 2020, Annals of Indian Academy of Neurology.

Phenotypic spectrum of CHARGE syndrome based on clinical characteristics

E. Ataman, F. Hazan, S. Gürsoy, 2018, Turkish journal of medical sciences.

Three novel mutations of CHD7 gene in two turkish patients with charge syndrome; A double point mutation and an insertion

E. Ataman, S. Gürsoy, A. Ulgenalp, 2015, Balkan journal of medical genetics : BJMG.

Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development

P. Gencpinar, E. Ataman, Nİhal OlgaÇ DÜndar, 2020, Turkish journal of medical sciences.

The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, Turkey.

E. Ataman, F. Ozkinay, A. Alpman, 2009, Genetic testing and molecular biomarkers.

The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey.

E. Ataman, F. Ozkinay, O. Cogulu, 2012, Genetic testing and molecular biomarkers.

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

J. Naggert, C. Möller, A. Çayır, 2014, Journal of Human Genetics.

The Multilingual Picture Database

Dušica Filipović Đurđević, H. Renvall, M. Ben-Shachar, 2022, Scientific Data.

A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel

B. Özkan, E. Ataman, F. Hazan, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Using Cognitive Apprenticeship to Enhance the Study of Budgeting and Budgetary Control: An Action Research1

B. Agyekum, E. Ataman, Ayuba Napari, 2020 .

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

J. Naggert, C. Möller, A. Çayır, 2015, Journal of Human Genetics.

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype.

E. Gulec, E. Ataman, Z. Ocak, 2015, International Journal of Cardiology.

The Processing of English-Turkish (False) Cognates: Evidence from a Backward Lexical Translation Task

B. Kırkıcı, E. Ataman, O. Çağlar, 2021, Cankaya University journal of humanities and social sciences.