A. Subaşıoğlu

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

A. Caglayan, O. Ozdemır, S. Artan, 2022, Functional & Integrative Genomics.

Genetic background of supernumerary teeth

M. Dundar, S. Savaş, A. Yagci, 2015, European journal of dentistry.

The effect of parental 5,10-methylenetetrahydrofolate reductase 677C/T and 1298A/C gene polymorphisms on response to single-dose methotrexate in tubal ectopic pregnancy

M. Dundar, S. Uludağ, M. S. Kutuk, 2017, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia

N. Ishiguro, H. Kitoh, Y. Nishida, 2015, Molecular Syndromology.

Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Non-Syndromic Deafness in a Large Multiethnic Cohort

M. Tekin, S. Blanton, Shengru Guo, 2015, Genetics in Medicine.

The effect of the additional cytogenetic abnormalities on major molecular response and BCR-ABL kinase domain mutations in long-term follow-up chronic myeloid leukemia patients, a cross sectional study

K. Savaşoğlu, F. Ozdemirkiran, A. Subaşıoğlu, 2017, Leukemia & lymphoma.

Emopamil Binding Protein Mutation in Conradi-Hünermann-Happle Syndrome Representing Plaque-Type Psoriasis

F. Ozkan, P. Ozturk, J. Cañueto, 2015, Indian Journal of Dermatology.

Radixin modulates the function of outer hair cell stereocilia

M. Tekin, G. Bademci, A. Fridberger, 2020, Communications biology.

Radixin modulates stereocilia function and contributes to cochlear amplification

M. Tekin, G. Bademci, A. Fridberger, 2020, bioRxiv.

Cavum Vergae: In the Differential Diagnosis of Fetal Midline Intracranial Cystic Lesions

T. Kalayci, U. Turhan, S. Kelekci, 2015, Journal of Pediatric Neuroradiology.

Treatment of three hereditary leiomyomatosis patients with cryotherapy

Belkız Uyar, E. Acar, A. Subaşıoğlu, 2020, Dermatologic therapy.

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations

M. Tekin, S. Blanton, G. Bademci, 2015, BMC Medical Genetics.

Research of genetic bases of hereditary non-syndromic hearing loss.

M. Tekin, D. Duman, G. Bademci, 2017, Turk pediatri arsivi.

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

M. Tekin, S. Blanton, R. Zhai, 2019, Proceedings of the National Academy of Sciences.

Genetic, Surgical and Oncological Approach to Breast Cancer, with BRCA1, BRCA2, CDH1, PALB2, PTEN and TP53 Variants.

M. Tekindal, M. Atahan, A. Subaşıoğlu, 2022, European journal of breast health.