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期刊名字![]() | Human Genomics HUM GENOMICS (此期刊被最新的JCR期刊SCIE收录) LetPub评分 6.4
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声誉 7.2 影响力 5.2 速度 9.1 | |||||||||||||||||||||||||||||
| 期刊ISSN | 1473-9542 | 蝌蝌APP,让您与同行交流更轻松
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| E-ISSN | 1479-7364 | |||||||||||||||||||||||||||||
| 2024-2025最新影响因子 (数据来源于搜索引擎) | 4.3 点击查看影响因子趋势图 | |||||||||||||||||||||||||||||
| 实时影响因子 | 截止2025年10月27日:3.065 | |||||||||||||||||||||||||||||
| 2024-2025自引率 | 2.3%点击查看自引率趋势图 | |||||||||||||||||||||||||||||
| 五年影响因子 | 4.2 | |||||||||||||||||||||||||||||
| JCI期刊引文指标 | 1.09 | |||||||||||||||||||||||||||||
| h-index | 49 | |||||||||||||||||||||||||||||
| 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.springer.com/journal/40246 | |||||||||||||||||||||||||||||
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/HUGM | |||||||||||||||||||||||||||||
| 该期刊中国学者近期发文 - New | CHEK1 variant is a risk factor for premature ovarian insufficiency by mis- regulating metabolism and inflammation-related genes Author: Guo, Jianying; Fan, Yali; Song, Zifan; Li, Lin; Fu, Meng Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00774-1 CLPP Gene Variants Causing Perrault Syndrome Type 3 in Han Chinese Families: A Genotype-Phenotype Study Author: Long, Xicui; Yang, Bingqian; Wang, Wei; Peng, Wan; Wang, Xiaolu; Xiong, Wenyu; Liu, Man; Yuan, Huijun; Lu, Yu Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00762-5 BAX-mediated ammonia-driven cell death: a novel prognostic and therapeutic target in clear cell renal cell carcinoma Author: Zhang, Xi; Yu, Zijie; Yin, Lu; Li, Qiang; He, Shaohua; Li, Heng; Li, Jian; Sheng, Lian; Wu, Hongfei; Chen, Hongqi; Zhu, Xiaoxu; Lv, Yang Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00764-3 Targeted multi-layer analysis of PANoptosis-associated genes in the etiology of chronic kidney disease Author: Li, Tong; Zhang, Yingyue; Wang, Xingzhi; Liu, Qi; Ma, Xiaofei; Sui, Manshu Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00768-z | |||||||||||||||||||||||||||||
| 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Human Genomics的语言要求,还能让Human Genomics编辑和审稿人得到更好的审稿体验,让稿件最大限度地被Human Genomics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 论文致谢 。
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( GBP2390; USD3190; EUR2690; ) 文章处理费豁免:查看说明 其他费用:没有 期刊主题关键词:genomic analysis、comparative genomics 相关链接:Aims & ScopeAuthor InstructionsEditorial BoardAnonymous peer review | |||||||||||||||||||||||||||||
| 通讯方式 | CAMPUS, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW | |||||||||||||||||||||||||||||
| 出版商 | BioMed Central | |||||||||||||||||||||||||||||
| 涉及的研究方向 | GENETICS & HEREDITY- | |||||||||||||||||||||||||||||
| 出版国家或地区 | ENGLAND | |||||||||||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||||||||||
| 出版周期 | ||||||||||||||||||||||||||||||
| 出版年份 | 2003 | |||||||||||||||||||||||||||||
| 年文章数 | 136点击查看年文章数趋势图 | |||||||||||||||||||||||||||||
| Gold OA文章占比 | 100.00% | |||||||||||||||||||||||||||||
| 研究类文章占比: 文章 ÷(文章 + 综述) | 91.18% | |||||||||||||||||||||||||||||
| WOS期刊JCR分区 ( 2024-2025年最新版) | WOS分区等级:1区
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| 中国科学院《国际期刊预警 名单(试行)》名单 | 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 | |||||||||||||||||||||||||||||
| 中国科学院期刊分区 ( 2025年3月最新升级版) | 点击查看中国科学院期刊分区趋势图
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| 中国科学院期刊分区 ( 2023年12月升级版) |
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| 中国科学院期刊分区 ( 2022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=1473-9542%5BISSN%5D | |||||||||||||||||||||||||||||
| 平均审稿速度 | 网友分享经验: 11 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( GBP2390; USD3190; EUR2690; ) 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Human Genomics顺利发表。
快看看作者怎么说吧:服务好评 论文致谢 。 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. | CHEK1 variant is a risk factor for premature ovarian insufficiency by mis- regulating metabolism and inflammation-related genes Author: Guo, Jianying; Fan, Yali; Song, Zifan; Li, Lin; Fu, Meng Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00774-1 PubMed DOI |
| 2. | CLPP Gene Variants Causing Perrault Syndrome Type 3 in Han Chinese Families: A Genotype-Phenotype Study Author: Long, Xicui; Yang, Bingqian; Wang, Wei; Peng, Wan; Wang, Xiaolu; Xiong, Wenyu; Liu, Man; Yuan, Huijun; Lu, Yu Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00762-5 PubMed DOI |
| 3. | BAX-mediated ammonia-driven cell death: a novel prognostic and therapeutic target in clear cell renal cell carcinoma Author: Zhang, Xi; Yu, Zijie; Yin, Lu; Li, Qiang; He, Shaohua; Li, Heng; Li, Jian; Sheng, Lian; Wu, Hongfei; Chen, Hongqi; Zhu, Xiaoxu; Lv, Yang Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00764-3 PubMed DOI |
| 4. | Targeted multi-layer analysis of PANoptosis-associated genes in the etiology of chronic kidney disease Author: Li, Tong; Zhang, Yingyue; Wang, Xingzhi; Liu, Qi; Ma, Xiaofei; Sui, Manshu Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00768-z PubMed DOI |
| 5. | Bioinformatics analysis of circular RNAs associated with atrial fibrillation and their evaluation as predictive biomarkers Author: Wang, Manman; Chen, Yuanyuan; Yang, Weiwei; Li, Xiangting; Liu, Genli; Wang, Xin; Liu, Shuai; Gao, Ge; Meng, Fanhua; Kong, Feifei; Sun, Dandan; Qin, Wei; Dong, Bo; Zhang, Jinguo Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00760-7 PubMed DOI |
| 6. | Genetic variants of m1A modification genes and the risk of neuroblastoma: novel insights from a Chinese case-control study Author: Chang, Jiaming; Lin, Lei; Zhang, Wenli; Yang, Jiliang; Zhang, Mengzhen; Yin, Huimin; Zhang, Xinxin; Zhou, Chunlei; Zou, Yan; He, Jing Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00767-0 PubMed DOI |
| 7. | Molecular genetic testing and cohort analysis of 32 twin pairs with neurodevelopmental disorders-Reporting a novel de novo variant of TET3 Author: Mei, Lianni; Hu, Chunchun; Jin, Guangbo; Ge, Chuanhui; Zhu, Yiting; Li, Dongyun; Peng, Wenzhu; Li, Huiping; Xu, Xiu; Jiang, Yan; Xu, Guoliang; Xu, Qiong Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00748-3 PubMed DOI |
| 8. | Functional analysis of a novel FOXL2 mutation in blepharophimosis, ptosis, and epicanthus inversus syndrome type II and elucidation of the genotype-phenotype correlation Author: Shen, Bingyan; Chen, Xi; Zhu, Xiuying; Chen, Ziwen; Fang, Yenan; Dai, Qin; Li, Xinyu; Xie, Qiqi; Wu, Wencan; Wang, Min Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00752-7 PubMed DOI |
| 9. | Reliability of clinical impressions and optimal genetic diagnostic strategies of heritable connective tissue disorders with ocular involvement in a large Chinese cohort Author: Shu, Qin-Meng; Ju, Yu-Qiao; Zong, Yuan; Zhang, Ting; Huang, Xin; Gao, Feng-juan; Chang, Qing Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00749-2 PubMed DOI |
| 10. | Clinical utility of trio whole exome sequencing in fetuses with ultrasound anomalies Author: Zeng, Ziye; Zhang, Lan; Zhou, Yuqin; Zhang, Xue; Yi, Hong; Li, He; Liu, Yuqi; Li, Jian; Chen, Qian; Chen, Yulin; Yu, Guiming; Yi, Jing; Zhang, Yana; Zhang, Hua; Dong, Yanling Journal: HUMAN GENOMICS. 2025; Vol. 19, Issue 1, pp. -. DOI: 10.1186/s40246-025-00745-6 PubMed DOI |
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