日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Effect of resveratrol on the antioxidant enzyme pathway and alveolar bone loss in experimental periodontitis

白藜芦醇对实验性牙周炎中抗氧化酶通路和牙槽骨丢失的影响

期刊:Acta Odontologica Scandinavica
影响因子:1.9
doi:10.2340/aos.v84.44956
Sezgin, Yasemin; Bilgin Çetin, Mehtap; Terzi, Yunus Kasim; Darcansoy İşeri, Özlem; Erinanç, Hilal; Şahin, Feride İffet; Bakırarar, Batuhan; Özerkliğ, İdil; Bulut, Şule; Alptekin, Nilgün Özlem
信号转导
发表日期：2025
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Homologous recombination deficiency gene panel analysis results in synchronous endometrial and ovarian cancers

同源重组缺陷基因检测结果显示子宫内膜癌和卵巢癌同步发生

期刊:Revista Da Associacao Medica Brasileira
影响因子:1.3
doi:10.1590/1806-9282.20240534
Kazanci, Ferah; Çelik, Zerrin Yılmaz; Polat, Mert; Karademir, Ferhat; Erdem, Ozlem; Şahin, Feride İffet; Onan, Mehmet Anil
卵巢癌
肿瘤
肿瘤免疫
子宫内膜癌
发表日期：2024
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Determination of the Frequency of BCL-2 Polymorphisms (c.-717C>A and c.*2364G>A) and LIF Polymorphism (c.*1414T>G) in Patients with Congenital Anomalies of the Kidney and Urinary Tract

测定先天性肾脏和泌尿系统畸形患者中BCL-2多态性（c.-717C>A和c.*2364G>A）和LIF多态性（c.*1414T>G）的频率

期刊:Molecular Syndromology
影响因子:0.9
doi:10.1159/000538653
Oztepe, Tugce; Sahin, Feride Iffet; Yilmaz, Aysun Caltik; Baskin, Esra; Haberal, Mehmet; Terzi, Yunus Kasim
LIF
发表日期：2024
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BRCA, infertility, and fertility preservation: a review for counseling

BRCA基因突变、不孕症和生育力保存：咨询指南

期刊:Journal of Assisted Reproduction and Genetics
影响因子:
doi:10.1007/s10815-023-02725-y
Baltacı, Ege; Kazancı, Ferah; Şahin, Feride İffet
发表日期：2023
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The Role of Heredity and the Prevalence of Strabismus in Families with Accommodative, Partial Accommodative, and Infantile Esotropia

遗传因素在调节性、部分调节性和婴儿型内斜视家族中的作用及斜视患病率

期刊:Turkish Journal of Ophthalmology
影响因子:
doi:10.4274/tjo.galenos.2019.49204
Çorak Eroğlu, Fatma; Oto, Sibel; Şahin, Feride İffet; Terzi, Yunus; Özer Kaya, Özge; Tekindal, Mustafa Agah
发表日期：2020
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Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles

致病突变及雄激素性葡萄胎的机制

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2018.10.007
Nguyen, Ngoc Minh Phuong; Ge, Zhao-Jia; Reddy, Ramesh; Fahiminiya, Somayyeh; Sauthier, Philippe; Bagga, Rashmi; Sahin, Feride Iffet; Mahadevan, Sangeetha; Osmond, Matthew; Breguet, Magali; Rahimi, Kurosh; Lapensee, Louise; Hovanes, Karine; Srinivasan, Radhika; Van den Veyver, Ignatia B; Sahoo, Trilochan; Ao, Asangla; Majewski, Jacek; Taketo, Teruko; Slim, Rima
免疫/内分泌
发表日期：2018
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Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients

遗传性血色素沉着症基因H63D和C282Y突变对镰状细胞病患者铁过载的影响

期刊:Turkish Journal of Hematology
影响因子:1.3
doi:10.4274/tjh.2015.0254
Terzi, Yunus Kasım; Bulakbaşı Balcı, Tuğçe; Boğa, Can; Koç, Zafer; Yılmaz Çelik, Zerrin; Özdoğu, Hakan; Karakuş, Sema; Şahin, Feride İffet
3D/类器官
细胞生物学
发表日期：2016
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West syndrome associated with a novel chromosomal anomaly; partial trisomy 8P together with partial monosomy 9P, resulting from a familial unbalanced reciprocal translocation

韦斯特综合征伴有新的染色体异常：8P部分三体和9P部分单体，由家族性不平衡相互易位引起。

期刊:Journal of Pediatric Neurosciences
影响因子:0.2
doi:10.4103/1817-1745.154324
Erol, Ilknur; Saygı, Semra; Demir, Şenay; Alehan, Fusun; Sahin, Feride Iffet
发表日期：2015
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Diagnosis of variant klinefelter syndrome in a 21-year-old male who presented with sparse facial hair

一名21岁男性患者因面部毛发稀疏就诊，被诊断为变异型克氏综合征。

期刊:
影响因子:
doi:10.5021/ad.2012.24.3.368
Purnak, Seda; Ada, Simin; Güleç, A Tülin; Balci, Tugce Bulakbasi; Sahin, Feride Iffet
发表日期：2012
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