Beren Karaosmanoglu
Beren Karaosmanoglu
Hacettepe University Faculty of Medicine Department of Medical Genetics
Verified email at - Homepage
Cited by
Cited by
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
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
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
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
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
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
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
Transcriptome analysis reveals differentially expressed genes between human primary bone marrow mesenchymal stem cells and human primary dermal fibroblasts
Turkish Journal of Biology 43 (1), 21-27, 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
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
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
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
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
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
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
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
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
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
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
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
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