| Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia ME Yildirim, HK Kurtulgan, O Ozdemir, H Kilicgun, DS Aydemir, B Baser, ... Annals of Saudi Medicine 39 (6), 382-387, 2019 | 22 | 2019 |
| The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study ME Yildirim, S Karakus, HK Kurtulgan, B Baser, I Sezgin Journal of gynecology obstetrics and human reproduction 48 (7), 521-525, 2019 | 17 | 2019 |
| Megacystis microcolon intestinal hypoperistalsis syndrome in which a different De Novo Actg2 gene mutation was detected: a case report EÜ Korğalı, A Yavuz, CEÇ Şimşek, C Güney, HK Kurtulgan, B Başer, ... Fetal and pediatric pathology 37 (2), 109-116, 2018 | 13 | 2018 |
| Ocular and genetic characteristics observed in two cases of fish-eye disease M Ustaoglu, N Solmaz, B Baser, HK Kurtulgan, F Onder Cornea 38 (3), 379-383, 2019 | 12 | 2019 |
| Identification of a novel pathogenic variant in CKAP2L and literature review in a child with Filippi syndrome and congenital talipes equinovarus T Karakaya, AE Bilgic, D Eris, B Baser, S Mermer, O Yildiz American Journal of Medical Genetics Part A 185 (7), 2198-2203, 2021 | 6 | 2021 |
| A boy with Sandestig-Stefanova syndrome and genital abnormalities A Korulmaz, B Başer, M Alakaya, AE Arslanköylü Molecular Syndromology 13 (4), 343-349, 2022 | 3 | 2022 |
| Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population İ Sezgin, M Kayataş, HK Kurtulgan, ME Yıldırım, B Başer, M Timuçin, ... Turkish journal of nephrology (Online) 29 (4), 304-309, 2020 | 3 | 2020 |
| The Association of MCP-1 Level and MCP-1-2518 A/G and CCR2 190 G/A Gene Polymorphisms with COPD and Pulmonary Hypertension. ME Yıldırım, S Berk, HK Kurtulgan, G Tekin, YK Tekin, B Başer, G Bağcı, ... Gazi Medical Journal 32 (1), 2021 | 1 | 2021 |
| Many Faces of Diencephalic-Mesencephalic Junction Dysplasia Syndrome with GSX2 and PCDH12 Variants G ÜREL DEMİR, B Başer, R GÖÇMEN, P ŞİMŞEK KİPER, G ÜTİNE, ... Molecular Syndromology, 2024 | | 2024 |
| EXTL3-Associated Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities: A Lethal Phenotype E Demir, F Adım, ME Döğen, A Aydoğdu, E Yeşil, S Mermer, B Başer, ... Pediatric Allergy, Immunology, and Pulmonology 36 (4), 147-149, 2023 | | 2023 |
| Coexistance of tetrasomy X and taurodontism: A case report. B Baser, HK Kurtulgan, ME Yildirim, I Sezgin Erciyes Medical Journal 41 (S1), 44-45, 2019 | | 2019 |
| İskelet Displazilerinde Genetik Danışma ve Prenatal Tanı İ SEZGİN, B BAŞER Turkiye Klinikleri Medical Genetics-Special Topics 4 (2), 97-104, 2019 | | 2019 |
| A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiency M YILDIRIM, A VURAL ÖZEÇ, H KÜÇÜK KURTULGAN, H KILIÇGÜN, ... JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE 9 (6), 2018 | | 2018 |
| 8q22. 3 q24. 23 duplication in a patient with oral frenulum and normal intellectual development HK Kurtulgan, ME Yildirim, B Baser, I Sezgin MOLECULAR CYTOGENETICS 10, 2017 | | 2017 |
| TET2 geni varyantlarının MULTİPL skleroz ile olası ilişkisi B Başer Tıp Fakültesi, 0 | | |
