Beren Karaosmanoğlu (Beren Karaosmanoglu, B Karaosmanoğlu)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 13

Top Venues

American journal of medical genetics. Part A

Molecular biology reports

Turkish journal of biology = Turk biyoloji dergisi

Journal of intellectual disability research : JIDR

Hacettepe University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Hacettepe University

Turkey

PHD :: Stem Cell Sciences

Hacettepe University

Turkey

MSC :: Faculty of Medicine Department of Medical Biology

Bilkent University

Turkey

BSC :: Molecular Biology and Genetics

Publications

Pelin Özlem Şimşek-Kiper, Beren Karaosmanoğlu, Ekim Zihni Taşkiran, Özlem Boybeyi Türer, Gülen Eda Utine, Tutku Soyer
A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia. American journal of medical genetics. Part A (2024)
Pelin Özlem Şimşek-Kiper, Beren Karaosmanoğlu, Ekim Zihni Taşkiran, Özlem Boybeyi Türer, Gülen Eda Utine, Tutku Soyer
A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia. American journal of medical genetics. Part A 194 (9) (2024)
Pelin Özlem Şimşek-Kiper, Beren Karaosmanoğlu, Ekim Zihni Taşkiran, Özlem Boybeyi Türer, Gülen Eda Utine, Tutku Soyer
A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia. American journal of medical genetics. Part A 194 (9) (2024)
Pelin Özlem Şimşek-Kiper, Beren Karaosmanoğlu, Ekim Zihni Taşkiran, Özlem Boybeyi Türer, Gülen Eda Utine, Tutku Soyer
A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia. American journal of medical genetics. Part A 194 (9) (2024)
Beren Karaosmanoğlu, Gozde Imren, M Samil Ozisin, Tuba Reçber, Pelin Ozlem Simsek Kiper, Goknur Haliloglu, Mehmet Alikaşifoğlu, Emirhan Nemutlu, Ekim Zihni Taşkiran, Gulen Eda Utine
Ex vivo disease modelling of Rett syndrome: the transcriptomic and metabolomic implications of direct neuronal conversion. Molecular biology reports 51 (1) (2024)
Akçahan Akalın, Pelin Özlem Şimsek Kiper, Ekim Zihni Taşkiran, Beren Karaosmanoğlu, Gülen Eda Utine, Koray Boduroglu
A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. American journal of medical genetics. Part A 191 (4) (2023)
Akçahan Akalın, Pelin Özlem Şimsek Kiper, Ekim Zihni Taşkiran, Beren Karaosmanoğlu, Gülen Eda Utine, Koray Boduroglu
A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. American journal of medical genetics. Part A 191 (4) (2023)
Akçahan Akalın, Pelin Özlem Şimsek Kiper, Ekim Zihni Taşkiran, Beren Karaosmanoğlu, Gülen Eda Utine, Koray Boduroglu
A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. American journal of medical genetics. Part A (2023)
Akçahan Akalın, Pelin Özlem Şimsek Kiper, Ekim Zihni Taşkiran, Beren Karaosmanoğlu, Gülen Eda Utine, Koray Boduroglu
A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. American journal of medical genetics. Part A 191 (4) (2023)
Jing-Yi Xue, Pelin O Simsek-Kiper, Gulen Eda Utine, Li Yan, Zheng Wang, Ekim Z Taskiran, Beren Karaosmanoğlu, Gozde Imren, Rahsan Gocmen, Gen Nishimura, Naomichi Matsumoto, Noriko Miyake, Shiro Ikegawa, Long Guo
Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis. Journal of human genetics 66 (6) (2021)
Tutku Soyer, Beren Karaosmanoğlu, Ekim Zihni Taşkiran, Pelin Özlem Şimşek Kiper, İbrahim Karnak, Koray Boduroğlu, Gülen Eda Utine
Biallelic ITGB4 variants in familial pyloric atresia without epidermolysis bullosa: Report of two families with five siblings. American journal of medical genetics. Part A 185 (11) (2021)
Ekim Zihni Taşkiran, Beren Karaosmanoğlu, C Koşukcu, G Ürel-Demir, Ö Akgün-Doğan, P Ö Şimşek-Kiper, M Alikaşifoğlu, K Boduroğlu, Gülen Eda Utine
Diagnostic yield of whole-exome sequencing in non-syndromic intellectual disability. Journal of intellectual disability research : JIDR 65 (6) (2021)
Ekim Zihni Taşkiran, Beren Karaosmanoğlu
Transcriptome analysis reveals differentially expressed genes between human primary bone marrow mesenchymal stem cells and human primary dermal fibroblasts. Turkish journal of biology = Turk biyoloji dergisi 43 (1) (2019)

Beren Karaosmanoğlu.css-eqlu8i{font-size:small;padding-left:4px;} (Beren Karaosmanoglu, B Karaosmanoğlu)

Publication Activity (10 Years)

Top Topics

Top Venues

Beren Karaosmanoğlu (Beren Karaosmanoglu, B Karaosmanoğlu)