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

Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies

研究线粒体和核基因组变异在儿童心肌病中的双重作用

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-025-01007-0
Temena, M Arda; Gokalp, Ebru Erzurumluoglu; Susam, Ezgi; Cinar, Duygu; Kiztanir, Hikmet; Kosger, Pelin; Aras, Beyhan Durak; Artan, Sevilhan; Cilingir, Oguz
心血管
线粒体
心肌病
发表日期：2025
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The Role of miRNA Expression Profiles in Different Biofluids in Aneurysm Rupture

miRNA表达谱在不同生物体液中对动脉瘤破裂的作用

期刊:Journal of Korean Neurosurgical Society
影响因子:1.7
doi:10.3340/jkns.2024.0171
Ansari, Sara Khadem; Gokalp, Ebru Erzurumluoglu; Ozkara, Emre; Aykac, Ozlem; Cilingir, Oguz; Colak, Ertugrul; Ozdemir, Atilla Ozcan; Artan, Sevilhan
miRNA
心血管
动脉瘤
发表日期：2025
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Comparison of conventional karyotype analysis and CMA results with ultrasound findings in pregnancies with normal QF-PCR results

将常规核型分析和染色体微阵列分析（CMA）结果与正常QF-PCR结果妊娠的超声检查结果进行比较

期刊:Turkish Journal of Obstetrics and Gynecology
影响因子:1.3
doi:10.4274/tjod.galenos.2025.10673
Bütün, Zafer; Kayapınar, Masum; Şenol, Gökalp; Akca, Ece; Erzurumluoğlu Gökalp, Ebru; Artan, Sevilhan
发表日期：2025
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A Novel de novo Exceptional Complex Chromosomal Rearrangement Involving 5 Chromosomes Resulting in Neurodevelopmental Delay and Dysmorphism

一种涉及5条染色体的全新从头发生的复杂染色体重排，导致神经发育迟缓和畸形

期刊:Molecular Syndromology
影响因子:0.9
doi:10.1159/000545465
Aynacı, Sabri; Kocagil, Sinem; Yarar, Coşkun; Tosumoğlu, Efsun; Gökalp, Ebru Erzurumluoğlu; Mutlu, Mehmet Burak; Artan, Sevilhan
发育与干细胞
神经科学
发表日期：2025
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Chromosomal abnormalities in couples with recurrent pregnancy loss: a 16-year cross-sectional study of 4030 cases from Turkey

土耳其一项为期16年、纳入4030例复发性流产夫妇的横断面研究：染色体异常

期刊:
影响因子:
doi:10.5144/0256-4947.2025.154
Aynaci, Sabri; Kocagil, Sinem; Tosumoglu, Esfun; Susam, Ezgi; Kilic, Betul; Gokalp, Ebru Erzurumluoglu; Cilingir, Oguz; Aras, Beyhan Durak; Tekin, Basar; Artan, Sevilhan
流产
发表日期：2025
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A novel mutation in RNF216 gene in a Turkish case with Gordon Holmes syndrome

土耳其一名患有戈登-霍姆斯综合征的患者体内发现RNF216基因的新突变

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-023-01529-4
Durmaz Çelik, Nazlı; Erzurumluoğlu, Ebru; Özben, Serkan; Toprak, Uğur; Yorulmaz, Göknur; Artan, Sevilhan; Özkan, Serhat
发表日期：2023
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Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature

RFWD3基因导致范可尼贫血W组疾病的进一步证据：文献中第二例病例的详细临床报告

期刊:Molecular Syndromology
影响因子:0.9
doi:10.1159/000531429
Kocagil, Sinem; Şafak, İkbal Nur; Saraç, Elif; Aydın, Can; Artan, Sevilhan; Kırel, Birgül
贫血
代谢
发表日期：2023
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Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients

土耳其患者房颤导管消融术后长期复发与房颤相关的遗传变异

期刊:Anatolian Journal of Cardiology
影响因子:1.5
doi:10.14744/AnatolJCardiol.2020.44082
Ulus, Taner; Dural, Muhammet; Meşe, Pelin; Yetmiş, Furkan; Mert, Kadir Uğur; Görenek, Bülent; Çilingir, Oğuz; Erzurumluoglu Gökalp, Ebru; Arslan, Serap; Artan, Sevilhan; Aykaç, Özlem; Çolak, Ertuğrul; Yorgun, Hikmet; Canpolat, Uğur; Aytemir, Kudret
发表日期：2021
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Comparison of the Apoptotic Effects of Topically Applied Papaverine, Diltiazem, and Nitroprusside to Internal Thoracic Artery

比较局部应用罂粟碱、地尔硫卓和硝普钠对内乳动脉细胞凋亡的影响

期刊:Revista Brasileira De Cirurgia Cardiovascular
影响因子:1.2
doi:10.21470/1678-9741-2019-0251
Unal, Orcun; Ulukan, Mustafa Ozer; Bakuy, Vedat; Kaytaz, Behiye; Artan, Sevilhan; Aral, Erinc; Oztas, Didem Melis; Beyaz, Metin Onur; Ugurlucan, Murat; Sevin, Behcet
细胞生物学
凋亡
表观遗传
发表日期：2020
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Screening of Cucurbita maxima and Cucurbita moschata Genotypes for Resistance Against Meloidogyne arenaria, M. incognita, M. javanica, and M. luci

筛选南瓜（Cucurbita maxima）和麝香南瓜（Cucurbita moschata）基因型对南方根结线虫（Meloidogyne arenaria）、南方根结线虫（M. incognita）、爪哇根结线虫（M. javanica）和光斑根结线虫（M. luci）的抗性

期刊:Journal of Nematology
影响因子:1.3
doi:10.21307/jofnem-2019-057
Aydınlı, Gökhan; Kurtar, Ertan Sait; Mennan, Sevilhan
发表日期：2019
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