Author

Yunus Kasım Terzi

Observed names: TERZİ, YUNUS KASIM, Terzi, Yunus, Terzi, Yunus Kasim, Y K Terzi, Y. K. Terzi, Y.K. Terzi, YUNUS TERZİ, Yunus K Terzi, Yunus K. Terzi, Yunus KASIM TERZİ, Yunus Kasim Terzi, Yunus Kasým Terzi, Yunus Kasım TERZİ, Yunus Kazim Terzi, Yunus Terzi

Institution: Başkent University

Observed institutions: Başkent University, Dokuz Eylül University, Yale Cancer Center, Yale University, Gülhane Askerî Tıp Akademisi, Ulucanlar Göz Eğitim ve Araştırma Hastanesi, Eskişehir Osmangazi University, Hacettepe University, Gazi University

ORCID: 0000-0001-5612-9696

Observed ORCID: 0000-0001-5612-9696

OpenAlex ID: A5073886732

A highly efficient and faithful MDS patient-derived xenotransplantation model for pre-clinical studies

2019 · Yuanbin Song, Anthony Rongvaux, et al. · Nature Communications · 94

beta-Adrenoreceptor antagonists reduce cancer cell proliferation, invasion, and migration

2014 · Özlem Darcansoy İşeri, Feride Iffet Sahin, et al. · Pharmaceutical Biology · 67

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Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene

2006 · Sibel Oguzkan, Yunus Kasım Terzi, et al. · Cancer Genetics and Cytogenetics · 24

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

2022 · Munis Dundar, Umut Fahrioglu, et al. · Functional & Integrative Genomics · 20

HOXA11 and MMP2 gene expression in uterosacral ligaments of women with pelvic organ prolapse

2014 · Nafiye Yilmaz, Gulnur Ozaksit, et al. · Journal of the Turkish-German Gynecological Association · 19

Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling.

2009 · Y K Terzi, S Oguzkan-Balci, et al. · PubMed · 18

Biochemical, Radiologic, Ultrastructural, and Genetic Evaluation of Iron Overload in Acute Leukemia and Iron-chelation Therapy

2013 · Lale Olcay, Tuncay Hazirolan, et al. · Journal of Pediatric Hematology/Oncology · 17

BRCA1 and BRCA2 sequence variations detected with next-generation sequencing in patients with premature ovarian insufficiency

2016 · Nafiye Karakas Yilmaz, Peren Hatice Karagin, et al. · Journal of the Turkish-German Gynecological Association · 14

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Coronin 1A inhibits neurite outgrowth in PC12 cells

2014 · Yunus Kasim Terzi, Yusuf Cetin Kocaefe, et al. · Neuroscience Letters · 14

Molecular genetic analyses in neurofibromatosis type 1 patients with tumors

2006 · Sibel Oguzkan, Yunus Kasim Terzi, et al. · Cancer Genetics and Cytogenetics · 12

Odontogenic effects of two calcium silicate-based biomaterials in human dental pulp cells

2018 · Emel Olga Onay, Erkan Yurtcu, et al. · Advances in Clinical and Experimental Medicine · 11

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Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients

2016 · Yunus Kasım Terzi, Tuğçe Bulakbaşı Balcı, et al. · Turkish Journal of Hematology · 11

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Lack of association of matrix metalloproteinase-9 promoter gene polymorphism in obstructive sleep apnea syndrome

2015 · Mustafa Yalcınkaya, Selim S. Erbek, et al. · Journal of Cranio-Maxillofacial Surgery · 11

Inhibition of the Notch Pathway Promotes Flap Survival by Inducing Functional Neoangiogenesis

2014 · Ozan Luay Abbas, Hüseyin Borman, et al. · Annals of Plastic Surgery · 11

Neurofibromatosis: Novel and Recurrent Mutations in Turkish Patients

2007 · Yunus Kasim Terzi, Sibel Oguzkan, et al. · Pediatric Neurology · 11

The impact of developmental genes in non-syndromic cleft lip and/or palate

2023 · Nihal Şahin Uysal, Feride İffet Şahin, et al. · Journal of the Turkish-German Gynecological Association · 10

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The Notch Signaling System Is Involved in the Regulation of Reparative Angiogenesis in the Zone of Stasis

2017 · Ozan Luay Abbas, Orhan Özatik, et al. · Journal of Burn Care & Research · 9

Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype

2011 · Yunus Kasim Terzi, Burcu Sirin, et al. · Child s Nervous System · 9

The Interaction between Childhood Maltreatment and Serotonin Transporter Gene in Recurrent Major Depressive Disorder: A Clinical Sample

2018 · Gamze Ozcurumez, Hasan Talha Yurdakul, et al. · Nöro Psikiyatri Arşivi · 8

The Notch pathway is a critical regulator of angiogenesis in a skin model of ischemia

2015 · Ozan L Abbas, Hüseyin Borman, et al. · Vascular Medicine · 8

FCN2 c.772G>T polymorphism is associated with chronic adenoiditis and/or tonsillitis, but not −4 A>G and −602 G>A

2016 · Alper N. Erkan, Isilay Oz, et al. · International Journal of Pediatric Otorhinolaryngology · 7

Retrieving relevant experiments: The case of microRNA microarrays

2015 · Koray Açıcı, Yunus Kasım Terzi, et al. · Biosystems · 7

Chronic tonsillitis is not associated with beta defensin 1 gene polymorphisms in Turkish population

2015 · Fatih Arslan, Seda Turkoglu Babakurban, et al. · International Journal of Pediatric Otorhinolaryngology · 7

Short and Long‐Term Outcomes of Liver Transplantation in Pediatric Patients With Inborn Errors of Metabolism: A Single‐Center Study

2025 · Hazel Delal Dara Kar, Halil İbrahim Aydın, et al. · Pediatric Transplantation · 6

Fractalkine receptor polymorphism and chronic tonsillitis

2014 · Seda Turkoglu Babakurban, Selim S. Erbek, et al. · European Archives of Oto-Rhino-Laryngology · 6

Works count: 72

Citation count: 480

H-index: 11

I10-index: 16