| 22q11 deletion syndrome: current perspective B Hacıhamdioğlu, D Hacıhamdioğlu, K Delil The application of clinical genetics, 123-132, 2015 | 116 | 2015 |
| JAGN1 deficient severe congenital neutropenia: two cases from the same family S Baris, E Karakoc–Aydiner, A Ozen, K Delil, A Kiykim, I Ogulur, I Baris, ... Journal of clinical immunology 35, 339-343, 2015 | 24 | 2015 |
| Challenges in the treatment of fibrodysplasia ossificans progressiva K Gencer-Atalay, EC Ozturk, I Yagci, P Ata, K Delil, Z Ozgen, G Akyuz Rheumatology international 39 (3), 569-576, 2019 | 20 | 2019 |
| Vitamin D receptor gene polymorphisms in children with kidney stone disease B Subasi, İ Gökçe, K Delil, H Alpay Turkish Journal of Pediatrics 59, 2017 | 12 | 2017 |
| Clinical report of a patient with de novo trisomy 12q23. 1q24. 33 BB Geckinli, H Aydin, A Karaman, K Delil, H Simsek, E Gokmeydan, ... Genet Couns 26 (4), 393-400, 2015 | 10 | 2015 |
| Two cases of acute myocarditis with multiple intracardiac thrombi: the role of hypercoagulable states H Atas, F Samadov, M Sunbul, A Cincin, K Delil, B Mutlu Heart Views 15 (1), 22-25, 2014 | 10 | 2014 |
| Investigation of SHOX gene mutations in Turkish patients with idiopathic short stature K Delil, HG Karabulut, B Hacıhamdioğlu, Z Şıklar, M Berberoğlu, G Öçal, ... Journal of clinical research in pediatric endocrinology 8 (2), 144, 2016 | 9 | 2016 |
| Biallelic mutations in DNAJB11 are associated with prenatal polycystic kidney disease in a Turkish family EA Ateş, A Turkyilmaz, K Delil, C Alavanda, MA Söylemez, BB Geçkinli, ... Molecular Syndromology 12 (3), 179-185, 2021 | 6 | 2021 |
| Functionally stable plasminogen activator inhibitor-1 in a family with cardiovascular disease and vitiligo M Agirbasli, M Eren, S Yasar, K Delil, F Goktay, ET Oner, DE Vaughan Journal of thrombosis and thrombolysis 38, 50-56, 2014 | 5 | 2014 |
| Acute inferior myocardial infarction in a patient with a prosthetic aortic valve and high international normalized ratio H Atas, I Sari, K Delil, C Ileri, F Samadov Advances in Interventional Cardiology/Postępy w Kardiologii Interwencyjnej …, 2014 | 4 | 2014 |
| Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report B Hacihamdioğlu, EG Baş, K Delil Journal of Clinical Research in Pediatric Endocrinology 13 (1), 100, 2021 | 3 | 2021 |
| Case of fatal heart failure with biventricular noncompaction, genital skeletal abnormalities and mental retardation H Atas, F Samadov, I Sari, K Delil The Anatolian Journal of Cardiology 15 (1), 71, 2015 | 2 | 2015 |
| Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis S Kalkan, MO Gürsoy, A Güner, S Gürsoy, M Kalçık, BB Geçkinli, K Delil, ... The American Journal of Cardiology 234, 22-29, 2025 | 1 | 2025 |
| Evaluation of BRCA1/BRCA2 test results for Turkish breast cancer families EA Ates, A Turkyilmaz, BB Geckinli, GG Ozgumus, MA Soylemez, K Delil, ... Erciyes Medical Journal 39 (2), S74-S74, 2017 | 1 | 2017 |
| Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report K DELİL GALENOS YAYINCILIK, 2021 | | 2021 |
| Novel Large CFTR Gene Deletions in Turkish Patients with Increased Morbidity P Ata, E Atag, Y Gokdemir, NB Ikizoglu, K Delil, E Eralp, P Ergenekon, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 980-980, 2018 | | 2018 |
| Evaluation of BRCA1/BRCA2 test results for Turkish breast cancer families EA Ates, A Turkyilmaz, BB Geckinli, GG Ozgumus, MA Soylemez, K Delil, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 966-966, 2018 | | 2018 |
| Inversion Y Having Different Phenotypic Expressions at Three Brothers A Turkyilmaz, P Ata, K Delil, S Soysal, EA Ates, AI Guney EUROPEAN JOURNAL OF HUMAN GENETICS 26, 829-829, 2018 | | 2018 |
| A novel HNF1B mutation in a family with two MODY patients EA Ates, A Turkyilmaz, BB Geckinli, MA Soylemez, K Delil, P Ata, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 863-863, 2018 | | 2018 |
| BBS10 frameshift mutation in a turkish girl with bardet biedl syndrome MA Soylemez, BB Geckinli, K Delil, E Ates, A Turkyilmaz, M Avsar, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 457-457, 2018 | | 2018 |
