| HERC1 mutations in idiopathic intellectual disability GE Utine, EZ Taşkıran, C Koşukcu, B Karaosmanoğlu, N Güleray, ... European journal of medical genetics 60 (5), 279-283, 2017 | 43 | 2017 |
| The effect of boron-containing nano-hydroxyapatite on bone cells M Gizer, S Köse, B Karaosmanoglu, EZ Taskiran, A Berkkan, M Timuçin, ... Biological Trace Element Research 193, 364-376, 2020 | 35 | 2020 |
| Human bone marrow mesenchymal stem cells secrete endocannabinoids that stimulate in vitro hematopoietic stem cell migration effectively comparable to beta-adrenergic stimulation S Köse, F Aerts-Kaya, ÇZ Köprü, E Nemutlu, B Kuşkonmaz, ... Experimental hematology 57, 30-41. e1, 2018 | 32 | 2018 |
| Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas B Karaosmanoglu, ÇY Kocaefe, F Söylemezoğlu, B Anlar, A Varan, ... Child's Nervous System 34, 877-882, 2018 | 19 | 2018 |
| Diagnostic yield of whole‐exome sequencing in non‐syndromic intellectual disability EZ Taşkıran, B Karaosmanoğlu, C Koşukcu, G Ürel‐Demir, ... Journal of Intellectual Disability Research 65 (6), 577-588, 2021 | 16 | 2021 |
| Small cell lung cancer stem cells display mesenchymal properties and exploit immune checkpoint pathways in activated cytotoxic T lymphocytes MA Kursunel, EZ Taskiran, E Tavukcuoglu, H Yanik, F Demirag, ... Cancer Immunology, Immunotherapy 71 (2), 445-459, 2022 | 14 | 2022 |
| Homozygous indel mutation in CDH11 as the probable cause of Elsahy–Waters syndrome EZ Taskiran, B Karaosmanoglu, C Koşukcu, ÖA Doğan, ... American Journal of Medical Genetics Part A 173 (12), 3143-3152, 2017 | 14 | 2017 |
| Transcriptome analysis reveals differentially expressed genes between human primary bone marrow mesenchymal stem cells and human primary dermal fibroblasts EZ TAŞKIRAN, B KARAOSMANOĞLU Turkish Journal of Biology 43 (1), 21-27, 2019 | 9 | 2019 |
| Two Siblings with Kaufman Oculocerebrofacial Syndrome Resembling Oculoauriculovertebral Spectrum G Ürel-Demir, B Aydın, B Karaosmanoğlu, Ö Akgün-Doğan, EZ Taşkıran, ... Molecular Syndromology 12 (2), 106-111, 2021 | 8 | 2021 |
| Novel insights into diabetes mellitus due to DNAJC3‐defect: Evolution of neurological and endocrine phenotype in the pediatric age group ZA Ozon, A Alikasifoglu, N Kandemir, B Aydin, EN Gonc, ... Pediatric Diabetes 21 (7), 1176-1182, 2020 | 8 | 2020 |
| An immunological and transcriptomics approach on differential modulation of NK cells in multiple sclerosis patients under interferon-β1 and fingolimod therapy NP Acar, A Tuncer, D Ozkazanc, FG Ozbay, B Karaosmanoglu, S Goksen, ... Journal of Neuroimmunology 347, 577353, 2020 | 8 | 2020 |
| Development, characterization and research of efficacy on in vitro cell culture of glucosamine carrying hyaluronic acid nanoparticles Ş Şahin, E Bilgiç, K Salimi, A Tuncel, B Karaosmanoğlu, EZ Taşkıran, ... Journal of Drug Delivery Science and Technology 52, 393-402, 2019 | 8 | 2019 |
| Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis JY Xue, PO Simsek-Kiper, GE Utine, L Yan, Z Wang, EZ Taskiran, ... Journal of Human Genetics 66 (6), 607-611, 2021 | 7 | 2021 |
| Molecular etiology of isolated congenital cataract using next-generation sequencing: single center exome sequencing data from Turkey H Taylan Sekeroglu, B Karaosmanoglu, EZ Taskiran, PO Simsek Kiper, ... Molecular Syndromology 11 (5-6), 302-308, 2020 | 7 | 2020 |
| Biallelic loss‐of‐function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo‐epi‐metaphyseal dysplasia with joint laxity … PO Simsek‐Kiper, P Jacob, P Upadhyai, ZE Taşkıran, VS Guleria, ... Human Mutation 43 (12), 2116-2129, 2022 | 5 | 2022 |
| A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features A Akalın, PÖ Şimşek‐Kiper, EZ Taşkıran, B Karaosmanoğlu, GE Utine, ... American Journal of Medical Genetics Part A 191 (4), 1119-1127, 2023 | 4 | 2023 |
| Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature B Karaosmanoglu, MA Kursunel, D Uckan Cetinkaya, F Gumruk, ... Frontiers in physiology, 727, 2021 | 4 | 2021 |
| Mutated Transcripts of ZEB2 Do Not Undergo Nonsense-Mediated Decay in Mowat-Wilson Syndrome N Güleray Lafcı, B Karaosmanoglu, EZ Taskiran, PO Simsek-Kiper, ... Molecular Syndromology 14 (3), 258-266, 2023 | 1 | 2023 |
| Biallelic ITGB4 variants in familial pyloric atresia without epidermolysis bullosa: Report of two families with five siblings T Soyer, B Karaosmanoglu, EZ Taskiran, PÖŞ Kiper, İ Karnak, ... American Journal of Medical Genetics Part A 185 (11), 3427-3432, 2021 | 1 | 2021 |
| Transcriptome and proteome profiles of human umbilical cord vein CD146+ stem cells B Gökçinar-Yagci, B Karaosmanoglu, EZ Taskiran, B Çelebi-Saltik Molecular biology reports 47, 3833-3856, 2020 | 1 | 2020 |
Ekim TaskiranHacettepe UniversityVerified email at hacettepe.edu.tr
