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期刊名字![]() | Frontiers in Genetics FRONT GENET (此期刊被最新的JCR期刊SCIE收录) LetPub评分 6.4
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声誉 6.7 影响力 5.6 速度 8.0 | |||||||||||||||||||||||||
| 期刊ISSN | 1664-8021 | 安装APP,查看期刊最新消息
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| 2025-2026最新IF (数据来源于网友提供) | 注册或登录后,查看IF | |||||||||||||||||||||||||
| 实时影响因子 | 截止2026年9月20日:1.815 | |||||||||||||||||||||||||
| 2025-2026自引率 | 3.3%点击查看自引率趋势图 | |||||||||||||||||||||||||
| 五年IF (数据来源于网友提供) | 3.301数据由网友[crazygamer254]收集提供 | |||||||||||||||||||||||||
| h-index | 61 | |||||||||||||||||||||||||
| CiteScore ( 2026年6月最新版) |
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| 期刊简介 |
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| 期刊官方网站 | https://www.frontiersin.org/journals/genetics | |||||||||||||||||||||||||
期刊投稿格式模板 VIP专享 |
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| 期刊投稿网址 | https://www.frontiersin.org/submission/SubmissionHome.aspx?domainId=1&fieldId=30&specialtyId=0&entityType=1&entityId=240 | |||||||||||||||||||||||||
| 该期刊中国学者近期发文 - New | Identification of ion homeostasis-related genes as diagnostic biomarkers for pulmonary arterial hypertension via WGCNA and machine learning Author: Chen, Yang; Chen, Qiu; Zheng, Senzhong Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1823486 Loss of lactate dehydrogenase A disrupts R-loop homeostasis and induces DNA damage in breast cancer cells Author: Li, Shangzhen; Xu, Cheng; Chen, Shuling; Yin, Guoping; Yang, Dawei Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1942597 The expressions and m6A methylation modification patterns of mRNAs and lncRNAs in major depressive disorder Author: Liu, Liang; Yang, Zhaonan; Tan, Kunru; Xu, Shuhao; Xu, Jia; Niu, Jinbao; Yang, Xiuxian Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1850052 Integrating single-cell multi-omics for precision radiotherapy stratification in hypopharyngeal squamous cell carcinoma Author: Zhang, Weishi; Yao, Mei Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1932515 | |||||||||||||||||||||||||
| 期刊语言要求 | 经LetPub语言功底雄厚的美籍native English speaker精心编辑的稿件,不仅能满足Frontiers in Genetics的语言要求,还能让Frontiers in Genetics编辑和审稿人得到更好的审稿体验,让稿件最大限度地被Frontiers in Genetics编辑和审稿人充分理解和公正评估。LetPub的专业SCI论文编辑服务(包括SCI论文英语润色,同行资深专家修改润色,SCI论文专业翻译,SCI论文格式排版,专业学术制图等)帮助作者准备稿件,已助力全球15万+作者顺利发表论文。部分发表范例可查看:服务好评(2篇) 论文致谢(17篇) 。
提交文稿 | |||||||||||||||||||||||||
| 是否OA开放访问 | Yes | |||||||||||||||||||||||||
OA期刊相关信息![]() | 文章处理费:需要( USD3295; ) 文章处理费豁免:查看说明 其他费用:没有 期刊主题关键词:gene、rna、genetic diseases、livestock and population genetics、epigenomics 相关链接:Aims & ScopeAuthor InstructionsEditorial BoardAnonymous peer review | |||||||||||||||||||||||||
| 通讯方式 | AVENUE DU TRIBUNAL FEDERAL 34, LAUSANNE, SWITZERLAND, CH-1015 | |||||||||||||||||||||||||
| 出版商 | Frontiers Media S.A. | |||||||||||||||||||||||||
| 涉及的研究方向 | Biochemistry, Genetics and Molecular Biology-Molecular Medicine | |||||||||||||||||||||||||
| 出版国家或地区 | UNITED STATES | |||||||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||||||
| 出版周期 | ||||||||||||||||||||||||||
| 出版年份 | 0 | |||||||||||||||||||||||||
| 年文章数 | 879点击查看年文章数趋势图 | |||||||||||||||||||||||||
| Gold OA文章占比 | 99.97% | |||||||||||||||||||||||||
| 研究类文章占比: 文章 ÷(文章 + 综述) | 90.44% | |||||||||||||||||||||||||
| WOS期刊JCR分区 ( 2025-2026年最新版) | 注册或登录后,查看WOS分区等级 | |||||||||||||||||||||||||
| 期刊分区表预警名单 | 2026年03月发布的新锐学术版:不在预警名单中 2025年03月发布的2025版:不在预警名单中 2024年02月发布的2024版:不在预警名单中 2023年01月发布的2023版:不在预警名单中 2021年12月发布的2021版:不在预警名单中 2020年12月发布的2020版:不在预警名单中 | |||||||||||||||||||||||||
| 《新锐期刊分区表》 ( 2026年3月发布) | 点击查看期刊分区表趋势图
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| 期刊分区表 ( 2025年3月升级版) |
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| 期刊分区表 ( 2023年12月旧的升级版) |
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| SCI期刊收录coverage | Science Citation Index Expanded (SCIE) (2020年1月,原SCI撤销合并入SCIE,统称SCIE) Scopus (CiteScore) Directory of Open Access Journals (DOAJ) | |||||||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1664-8021%5BISSN%5D | |||||||||||||||||||||||||
| 平均审稿速度 | 网友分享经验: 14 Weeks | |||||||||||||||||||||||||
| 平均录用比例 | 网友分享经验: | |||||||||||||||||||||||||
| 版面费/APC文章处理费信息 | 文章处理费:需要( USD3295; ) 文章处理费豁免:查看说明 其他费用:没有 LetPub提供文章处理费(APC)支持服务,可以用人民币支付版面费啦! | |||||||||||||||||||||||||
| LetPub助力发表 | 经LetPub编辑的稿件平均录用比例是未经润色的稿件的1.5倍,平均审稿时间缩短40%。众多作者在使用LetPub的专业SCI论文编辑服务(包括SCI论文英语润色,同行资深专家修改润色,SCI论文专业翻译,SCI论文格式排版,专业学术制图等)后论文在Frontiers in Genetics顺利发表。
快看看作者怎么说吧:服务好评(2篇) 论文致谢(17篇) 。 提交文稿 | |||||||||||||||||||||||||
| 期刊常用信息链接 |
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| 中国学者近期发表的论文 | |
| 1. | Identification of ion homeostasis-related genes as diagnostic biomarkers for pulmonary arterial hypertension via WGCNA and machine learning Author: Chen, Yang; Chen, Qiu; Zheng, Senzhong Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1823486 DOI |
| 2. | Loss of lactate dehydrogenase A disrupts R-loop homeostasis and induces DNA damage in breast cancer cells Author: Li, Shangzhen; Xu, Cheng; Chen, Shuling; Yin, Guoping; Yang, Dawei Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1942597 DOI |
| 3. | The expressions and m6A methylation modification patterns of mRNAs and lncRNAs in major depressive disorder Author: Liu, Liang; Yang, Zhaonan; Tan, Kunru; Xu, Shuhao; Xu, Jia; Niu, Jinbao; Yang, Xiuxian Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1850052 DOI |
| 4. | Integrating single-cell multi-omics for precision radiotherapy stratification in hypopharyngeal squamous cell carcinoma Author: Zhang, Weishi; Yao, Mei Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1932515 DOI |
| 5. | A rare de novo contiguous 15q11.1-q13.3 duplication with tetrasomy (CN=4) and adjacent trisomy (CN=3) associated with severe global developmental delay, autism spectrum disorder, and subclinical epileptiform discharges: a case report and literature review Author: Zhou, Xinyu; Xie, HongYan; Yu, Haoyan; Zhang, Zhiyuan; Qi, Yangfan; Jiang, Kai; Lin, Shuangzhu Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1953023 DOI |
| 6. | Computational prioritization of candidate TCDD-associated targets in retinoblastoma using network toxicology and transcriptomic analysis Author: Wang, Yingluan; Hu, Qiang; Cao, Zhan; Ye, Dian; Sun, Dawei; Qu, Lijun Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1911449 DOI |
| 7. | Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study Author: Tong, Jiao; Chen, Xu; Wang, Tao; Ma, Shan; Zhao, Yali; Shi, Dongdong; Wang, Xin; Yan, Dongmei Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1866451 DOI |
| 8. | Integrative bioinformatics and in vivo validation suggest a potential role of Cbr4 in alcohol use disorder through modulation of lipid metabolism and treg cell function in the central amygdala (vol 17, 1829878, 2026) Author: Ge, Yao; Yuan, Yihan; Li, Min; Huang, Zhenxia; Zhang, Chenli; Yu, Caiyu; Xu, Jinyu; Zhang, Siao; Guo, Hongwei; Zhang, Xu; Fu, Rao; Ren, Zhiheng Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1975571 DOI |
| 9. | Case Report: Presymptomatic risdiplam in preterm monozygotic twins with co-occurring spinal muscular atrophy and tuberous sclerosis complex Author: Zhang, Xiao-fang; Wang, Yan-juan; Li, Si-xiu; Liu, Ping; Hu, Wen-Guang Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1851666 DOI |
| 10. | Ultrasound radiomics integrated with an immune-related gene signature for predicting response and resistance to immune checkpoint inhibitors in cutaneous melanoma: a retrospective radiogenomic study with biological validation Author: Peng, Jinyu; Dai, Bowen; Ze, Kan; Yang, Jie Journal: FRONTIERS IN GENETICS. 2026; Vol. 17, Issue , pp. -. DOI: 10.3389/fgene.2026.1920615 DOI |
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