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

Editorial: The importance of faculty development in medical education

社论：教师发展在医学教育中的重要性

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2026.1798159
Pereza, Nina; Hauser, Goran; Jovanović, Predrag
发表日期：2026
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How to create a faculty development program that transforms medical education according to actual institutional needs: evidence-based approach and experience at the University of Rijeka, Faculty of Medicine, Croatia

如何根据实际的机构需求创建能够变革医学教育的教师发展项目：基于证据的方法和克罗地亚里耶卡大学医学院的经验

期刊:Frontiers in Medicine
影响因子:3
doi:10.3389/fmed.2025.1513119
Pereza, Nina; Hauser, Goran; Dević Pavlić, Sanja; Marić, Ivana; Sotošek, Vlatka; Grgasović, Tina; Mršić-Pelčić, Jasenka
发表日期：2025
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Protective Effect of EBF Transcription Factor 1 (EBF1) Polymorphism in Sporadic and Familial Spontaneous Preterm Birth: Insights from a Case-Control Study

EBF转录因子1 (EBF1) 多态性对散发性和家族性自发性早产的保护作用：一项病例对照研究的启示

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms252011192
Mladenić, Tea; Wagner, Jasenka; Kadivnik, Mirta; Pereza, Nina; Ostojić, Saša; Peterlin, Borut; Dević Pavlić, Sanja
发表日期：2024
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MTHFR Gene Polymorphisms and DNA Methylation in Idiopathic Spontaneous Preterm Birth

MTHFR基因多态性和DNA甲基化与特发性自发性早产的关系

期刊:Medicina-Lithuania
影响因子:2.4
doi:10.3390/medicina60122028
Dević Pavlić, Sanja; Šverko, Roberta; Barišić, Anita; Mladenić, Tea; Vraneković, Jadranka; Stanković, Aleksandra; Peterlin, Ana; Peterlin, Borut; Ostojić, Saša; Pereza, Nina
DNA甲基化
表观遗传
DNA甲基化
发表日期：2024
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Editorial: The Importance of Genetic Literacy and Education in Medicine

社论：遗传素养和教育在医学中的重要性

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2022.910530
Pereza, Nina; Peterlin, Borut; Ostojić, Saša; Poslon, Željka
发表日期：2022
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A Novel Likely Pathogenic Variant in the RUNX1 Gene as the Cause of Congenital Thrombocytopenia

RUNX1基因中一种新的可能致病变异是先天性血小板减少症的病因

期刊:Balkan Journal of Medical Genetics
影响因子:0.9
doi:10.2478/bjmg-2022-0009
Despotović, M; Pereza, N; Peterlin, B; Ostojić, S; Golob, B; Maver, A; Roganović, J
血小板
RUNX1
发表日期：2022
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The impact of needs-based education on the change of knowledge and attitudes towards medical genetics in medical students

需求导向型教育对医学生医学遗传学知识和态度转变的影响

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-020-00791-9
Čargonja, Paola; Mavrinac, Martina; Ostojić, Saša; Pereza, Nina
发表日期：2021
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Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages

巴尔干地区斯拉夫语系国家医学院校医学生遗传学基础和临床必修课程现状

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2021.793834
Pereza, Nina; Terzić, Rifet; Plaseska-Karanfilska, Dijana; Miljanović, Olivera; Novaković, Ivana; Poslon, Željka; Ostojić, Saša; Peterlin, Borut
发表日期：2021
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DNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking status

DNMT3B rs1569686 和 rs2424913 基因多态性与早产家族史和吸烟状况相关。

期刊:Croatian Medical Journal
影响因子:2.3
doi:10.3325/cmj.2020.61.8
Barišić, Anita; Kolak, Maja; Peterlin, Ana; Tul, Nataša; Gašparović Krpina, Milena; Ostojić, Saša; Peterlin, Borut; Pereza, Nina
发表日期：2020
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Vitamin D receptor polymorphisms in spontaneous preterm birth: a case-control study

自发性早产与维生素D受体多态性：一项病例对照研究

期刊:Croatian Medical Journal
影响因子:2.3
doi:10.3325/cmj.2020.61.338
Gašparović Krpina, Milena; Barišić, Anita; Peterlin, Ana; Tul, Nataša; Ostojić, Saša; Peterlin, Borut; Pereza, Nina
信号转导
发表日期：2020
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