| A highly efficient and faithful MDS patient-derived xenotransplantation model for pre-clinical studies Y Song, A Rongvaux, A Taylor, T Jiang, T Tebaldi, K Balasubramanian, ... Nature communications 10 (1), 366, 2019 | 78 | 2019 |
| beta-Adrenoreceptor antagonists reduce cancer cell proliferation, invasion, and migration ÖD İşeri, FI Sahin, YK Terzi, E Yurtcu, SR Erdem, F Sarialioglu Pharmaceutical biology 52 (11), 1374-1381, 2014 | 64 | 2014 |
| HOXA11 and MMP2 gene expression in uterosacral ligaments of women with pelvic organ prolapse N Yılmaz, G Ozaksit, YK Terzi, S Yılmaz, B Budak, O Aksakal, Fİ Şahin Journal of the Turkish German Gynecological Association 15 (2), 104, 2014 | 33 | 2014 |
| Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene S Oguzkan, YK Terzi, E Güler, M Derbent, PI Agras, U Saatci, S Ayter Cancer genetics and cytogenetics 164 (2), 159-163, 2006 | 24 | 2006 |
| Biochemical, radiologic, ultrastructural, and genetic evaluation of iron overload in acute leukemia and iron-chelation therapy L Olcay, T Hazirolan, Y Yildirmak, E Erdemli, YK Terzi, K Arda, ... Journal of Pediatric Hematology/Oncology 36 (4), 281-292, 2014 | 22 | 2014 |
| Reproductive decisions after prenatal dianosis in neurofibromatosis type 1: Importance of genetic counseling YK Terzi, S Oguzkan-Balci, B Anlar, S Aysun, S Guran, S Ayter Genetic Counseling 20 (2), 195, 2009 | 22 | 2009 |
| Molecular genetic analyses in neurofibromatosis type 1 patients with tumors S Oguzkan, YK Terzi, M Cinbis, B Anlar, S Aysun, S Ayter Cancer genetics and cytogenetics 165 (2), 167-171, 2006 | 20 | 2006 |
| BRCA1 and BRCA2 sequence variations detected with next-generation sequencing in patients with premature ovarian insufficiency NK Yılmaz, PH Karagin, YK Terzi, İ Kahyaoğlu, S Yılmaz, S Erkaya, ... Journal of the Turkish German Gynecological Association 17 (2), 77, 2016 | 17 | 2016 |
| Neurofibromatosis: novel and recurrent mutations in Turkish patients YK Terzi, S Oguzkan, B Anlar, S Aysun, S Ayter Pediatric neurology 37 (6), 421-425, 2007 | 16 | 2007 |
| Inhibition of the notch pathway promotes flap survival by inducing functional neoangiogenesis OL Abbas, H Borman, YK Terzi, A Terzi, N Bayraktar, B Özkan, AC Yazici Annals of plastic surgery 75 (4), 455-462, 2015 | 15 | 2015 |
| Coronin 1A inhibits neurite outgrowth in PC12 cells YK Terzi, YC Kocaefe, S Ayter Neuroscience Letters 582, 38-42, 2014 | 14 | 2014 |
| Chronic tonsillitis is not associated with beta defensin 1 gene polymorphisms in Turkish population F Arslan, ST Babakurban, SS Erbek, FI Sahin, YK Terzi International Journal of Pediatric Otorhinolaryngology 79 (4), 557-560, 2015 | 13 | 2015 |
| Retrieving relevant experiments: The case of microRNA microarrays K Açıcı, YK Terzi, H Oğul Biosystems 134, 71-78, 2015 | 11 | 2015 |
| Fractalkine receptor polymorphism and chronic tonsillitis ST Babakurban, SS Erbek, YK Terzi, F Arslan, FI Sahin European Archives of Oto-Rhino-Laryngology 271, 2045-2048, 2014 | 11 | 2014 |
| Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ... Functional & integrative genomics 22 (3), 291-315, 2022 | 10 | 2022 |
| FCN2 c. 772G> T polymorphism is associated with chronic adenoiditis and/or tonsillitis, but not− 4 A> G and− 602 G> A AN Erkan, I Oz, YK Terzi, E Aydin, M Ozkale, ST Babakurban, A Koycu, ... International journal of pediatric otorhinolaryngology 87, 1-4, 2016 | 9 | 2016 |
| Effect of hereditary hemochromatosis gene H63D and C282Y mutations on iron overload in sickle cell disease patients YK Terzi, T Bulakbaşı Balcı, C Boğa, Z Koç, Z Yılmaz Çelik, H Özdoğu, ... | 9 | 2016 |
| Lack of association of matrix metalloproteinase-9 promoter gene polymorphism in obstructive sleep apnea syndrome M Yalcınkaya, SS Erbek, ST Babakurban, E Kupeli, S Bozbas, YK Terzi, ... Journal of Cranio-Maxillofacial Surgery 43 (7), 1099-1103, 2015 | 9 | 2015 |
| Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype YK Terzi, B Sirin, G Hosgor, E Serdaroglu, B Anlar, S Aysun, S Ayter Child's Nervous System 28, 943-946, 2012 | 9 | 2012 |
| Learning disability and oligodendrocyte myelin glycoprotein (OMGP) gene in neurofibromatosis type 1 YK Terzi, S Oğuzkan-Balci, B Anlar, E Erdoğan-Bakar, S Ayter The Turkish Journal of Pediatrics 53 (1), 75-78, 2011 | 9 | 2011 |
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