Beren Karaosmanoglu
Hacettepe Üniversitesi
H-index: 8
Asia-Turkey
Top articles of Beren Karaosmanoglu
AP-1-Dependent Fibrosis: Exploring its Potential Role in the Pathogenesis of Placental Transmogrification of the Lung (PTL) via Tissue-Level Transcriptome Analysis
Pathology-Research and Practice
2024/4/26
A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia
American Journal of Medical Genetics Part A
2024/4/22
Acquired immune resistance is associated with interferon signature and modulation of KLF6/c‐MYB transcription factors in myeloid leukemia
European Journal of Immunology
2024/3/11
Beren Karaosmanoglu
H-Index: 5
Allele-specific antisense oligonucleotides for the treatment of BEST1-Related dominantly inherited retinal diseases: An in vitro model
Experimental Eye Research
2024/2/16
Beren Karaosmanoglu
H-Index: 5
Biomedical Efficacy of Garlic‐Extract‐Loaded Core‐Sheath Plasters for Natural Antimicrobial Wound Care
Macromolecular Materials and Engineering
2024
Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families
Molecular Syndromology
2024
CHRND variant in a paternally inherited esophageal atresia and tracheoesophgageal fistula: Report of a case
Birth Defects Research
2024/1
Mutated Transcripts of ZEB2 Do Not Undergo Nonsense-Mediated Decay in Mowat-Wilson Syndrome
Molecular Syndromology
2023/5/31
Beren Karaosmanoglu
H-Index: 5
Pelin Ozlem Simsek-Kiper
H-Index: 17
Neonatal ichthyosis–sclerosing cholangitis syndrome: report of a novel mutation and a review of the literature
2023/4/1
A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features
American Journal of Medical Genetics Part A
2023/4
Biallelic loss‐of‐function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo‐epi‐metaphyseal dysplasia with joint laxity …
2022/12
Small cell lung cancer stem cells display mesenchymal properties and exploit immune checkpoint pathways in activated cytotoxic T lymphocytes
Cancer Immunology, Immunotherapy
2022/2
The rare reason of pain in hip girdle: Mucolipidosis type 3 gamma
The Turkish Journal of Pediatrics
2021/12/25
Biallelic ITGB4 variants in familial pyloric atresia without epidermolysis bullosa: Report of two families with five siblings
American Journal of Medical Genetics Part A
2021/11
Tutku Soyer
H-Index: 11
Beren Karaosmanoglu
H-Index: 5
Diagnostic yield of whole‐exome sequencing in non‐syndromic intellectual disability
Journal of Intellectual Disability Research
2021/6
Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis
Journal of Human Genetics
2021/6
Li Yan
H-Index: 4
Zheng Wang
H-Index: 55
Beren Karaosmanoglu
H-Index: 5
Rahsan Gocmen
H-Index: 12
Naomichi Matsumoto
H-Index: 56
Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature
Frontiers in physiology
2021
Beren Karaosmanoglu
H-Index: 5
Fatma Gumruk
H-Index: 12
Two Siblings with Kaufman Oculocerebrofacial Syndrome Resembling Oculoauriculovertebral Spectrum
Molecular Syndromology
2021/4/22
Molecular etiology of isolated congenital cataract using next-generation sequencing: single center exome sequencing data from Turkey
Molecular Syndromology
2020/12/18
Novel insights into diabetes mellitus due to DNAJC3‐defect: Evolution of neurological and endocrine phenotype in the pediatric age group
Pediatric Diabetes
2020/11
