2026年3月最新《新锐期刊分区表》数据已更新，欢迎查询使用。如果您对期刊系统有任何需求或者问题，欢迎反馈给我们。
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| 基本信息 | 登录收藏 | |||||||||||||||||||||
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期刊名字 | GENE GENE （此期刊被最新的JCR期刊SCIE收录） LetPub评分 7.0
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声誉 7.6 影响力 6.1 速度 8.3 | |||||||||||||||||||||
| 期刊ISSN | 0378-1119 | 安装APP，查看期刊最新消息
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| E-ISSN | 1879-0038 | |||||||||||||||||||||
| 2024-2025最新影响因子 （数据来源于搜索引擎） | 2.4 点击查看影响因子趋势图 | |||||||||||||||||||||
| 实时影响因子 | 截止2026年5月06日：2.71 | |||||||||||||||||||||
| 2024-2025自引率 | 0.0%点击查看自引率趋势图 | |||||||||||||||||||||
| 五年影响因子 | 2.8 | |||||||||||||||||||||
| JCI期刊引文指标 | 0.72 | |||||||||||||||||||||
| h-index | 164 | |||||||||||||||||||||
| CiteScore （ 2025年最新版） |
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| 期刊简介 |
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| 期刊官方网站 | https://www.journals.elsevier.com/gene | |||||||||||||||||||||
期刊投稿格式模板 VIP专享 |
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| 期刊投稿网址 | https://www.editorialmanager.com/GENEJOURNAL | |||||||||||||||||||||
| 该期刊中国学者近期发文 - New | De novo SEC61A1 mutation in congenital anemia and early-onset kidney disease: Case report and review of the literature Author: Zhong, Linqing; Ding, Juan; Ma, Mingsheng; Wang, Changyan; Xiao, Juan; Wei, Min; Jian, Shan Journal: GENE. 2026; Vol. 993, Issue , pp. -. DOI: 10.1016/j.gene.2026.150106 Deubiquitination-driven adaptive programs in hepatocellular carcinoma: The emerging role of USP22 in hypoxia, metabolic rewiring, and drug resistance Author: Mei, Haohao; Yan, Ni Journal: GENE. 2026; Vol. 993, Issue , pp. -. DOI: 10.1016/j.gene.2026.150107 Syntaphilin inhibits glioma invasion via modulating mitochondria redistribution and shapes the immune microenvironment: A potential prognostic biomarker Author: Tian, Hui; Chen, Xuan; Si, Mingbin; Xu, Wenzhe Journal: GENE. 2026; Vol. 993, Issue , pp. -. DOI: 10.1016/j.gene.2026.150105 Identification and drug metabolic activity evaluation of 12 CYP2D6 allelic variants newly detected in the Chinese population Author: Chen, Chunhong; Geng, Peiwu; Liu, Rucong; Lu, Zebei; Lin, Qinrong; Ma, Yuntong; Han, Aixia; Zhang, Qiaoling; Wu, Shangqing; Jin, Pengfei; Xu, Wenfeng; Cai, Jianping; Wang, Shuanghu; Dai, Dapeng Journal: GENE. 2026; Vol. 992, Issue , pp. -. DOI: 10.1016/j.gene.2026.150094 | |||||||||||||||||||||
| 期刊语言要求 | Language Please write your text in good English (American or British usage is accepted, but not a mixture of these). Authors who feel their English language manuscript may require editing to eliminate possible grammatical or spelling errors and to conform to correct scientific English may wish to use the English Language Editing service. 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GENE的语言要求，还能让GENE编辑和审稿人得到更好的审稿体验，让稿件最大限度地被GENE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（13篇） 。 提交文稿 | |||||||||||||||||||||
| 是否OA开放访问 | No | |||||||||||||||||||||
| 通讯方式 | ELSEVIER SCIENCE BV, PO BOX 211, AMSTERDAM, NETHERLANDS, 1000 AE | |||||||||||||||||||||
| 出版商 | Elsevier | |||||||||||||||||||||
| 涉及的研究方向 | 生物-遗传学 | |||||||||||||||||||||
| 出版国家或地区 | NETHERLANDS | |||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||
| 出版周期 | Semimonthly | |||||||||||||||||||||
| 出版年份 | 1976 | |||||||||||||||||||||
| 年文章数 | 759点击查看年文章数趋势图 | |||||||||||||||||||||
| Gold OA文章占比 | 11.26% | |||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 91.96% | |||||||||||||||||||||
| WOS期刊JCR分区 （ 2024-2025年最新版） | WOS分区等级：3区
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| 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) | |||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0378-1119%5BISSN%5D | |||||||||||||||||||||
| 平均审稿速度 | 网友分享经验： 平均2.0月 | |||||||||||||||||||||
| 平均录用比例 | 网友分享经验： 约55.76% | |||||||||||||||||||||
| 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GENE顺利发表。
快看看作者怎么说吧：服务好评（2篇） 论文致谢（13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. | De novo SEC61A1 mutation in congenital anemia and early-onset kidney disease: Case report and review of the literature Author: Zhong, Linqing; Ding, Juan; Ma, Mingsheng; Wang, Changyan; Xiao, Juan; Wei, Min; Jian, Shan Journal: GENE. 2026; Vol. 993, Issue , pp. -. DOI: 10.1016/j.gene.2026.150106 PubMed DOI |
| 2. | Deubiquitination-driven adaptive programs in hepatocellular carcinoma: The emerging role of USP22 in hypoxia, metabolic rewiring, and drug resistance Author: Mei, Haohao; Yan, Ni Journal: GENE. 2026; Vol. 993, Issue , pp. -. DOI: 10.1016/j.gene.2026.150107 PubMed DOI |
| 3. | Syntaphilin inhibits glioma invasion via modulating mitochondria redistribution and shapes the immune microenvironment: A potential prognostic biomarker Author: Tian, Hui; Chen, Xuan; Si, Mingbin; Xu, Wenzhe Journal: GENE. 2026; Vol. 993, Issue , pp. -. DOI: 10.1016/j.gene.2026.150105 PubMed DOI |
| 4. | Identification and drug metabolic activity evaluation of 12 CYP2D6 allelic variants newly detected in the Chinese population Author: Chen, Chunhong; Geng, Peiwu; Liu, Rucong; Lu, Zebei; Lin, Qinrong; Ma, Yuntong; Han, Aixia; Zhang, Qiaoling; Wu, Shangqing; Jin, Pengfei; Xu, Wenfeng; Cai, Jianping; Wang, Shuanghu; Dai, Dapeng Journal: GENE. 2026; Vol. 992, Issue , pp. -. DOI: 10.1016/j.gene.2026.150094 PubMed DOI |
| 5. | miR-146a-3p drives major depressive disorder pathogenesis via BDNF suppression: a novel diagnostic and therapeutic target Author: Sun, Kangjun; Qin, Tong; Kang, Zhenhui Journal: GENE. 2026; Vol. 992, Issue , pp. -. DOI: 10.1016/j.gene.2026.150095 PubMed DOI |
| 6. | Distinct BNC1 variants contribute to premature ovarian insufficiency through different molecular mechanisms Author: Zheng, Zhi; Chu, Chunfang; Zhao, Minying; Sun, Yujun; Chen, Shuya; Li, Yuxiao; He, Lin; Xin, Mingwei; Li, Lin Journal: GENE. 2026; Vol. 992, Issue , pp. -. DOI: 10.1016/j.gene.2026.150104 PubMed DOI |
| 7. | LncRNA GAS5 regulates apoptosis in ovarian cancer cells by regulating O-GlcNAcylation of GOLGA8B Author: Chen, Renlin; Wang, Jiao; Wang, Zeyu; Zhao, Guoxia; Zhang, Jingjing; Liu, Weihe; Wang, Yan Journal: GENE. 2026; Vol. 991, Issue , pp. -. DOI: 10.1016/j.gene.2026.150084 PubMed DOI |
| 8. | Transcriptome analysis of patients with loss-of-function POGZ variants in four unrelated Chinese families Author: Wu, Yong; Liang, Na; He, Fengyuan; Tan, Bo Journal: GENE. 2026; Vol. 991, Issue , pp. -. DOI: 10.1016/j.gene.2026.150070 PubMed DOI |
| 9. | Association of C5AR1 polymorphisms with increased gastric cancer risk: mechanistic insights and therapeutic implications targeting JAK/ STAT pathway Author: Wang, Zhongqi; Jian, Ying; Jiang, Xiaomei; Zhang, Hongmei; Zhang, Zhi; Zhang, Xuemei Journal: GENE. 2026; Vol. 991, Issue , pp. -. DOI: 10.1016/j.gene.2026.150086 PubMed DOI |
| 10. | A closed-loop microfluidic platform for enhanced gut organoid maturation via physicochemical control and morphodynamic feedback Author: Owusu, Eric Kwame; Sinzinkayo, Donatien; Wang, Yue; Liu, Na; Yue, Tao Journal: GENE. 2026; Vol. 991, Issue , pp. -. DOI: 10.1016/j.gene.2026.150074 PubMed DOI |
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