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基本信息 | 登录收藏 | |||||||||||||||||||||
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期刊名字![]() | HUMAN GENETICS HUM GENET (此期刊被最新的JCR期刊SCIE收录) LetPub评分 7.7
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声誉 8.6 影响力 6.6 速度 9.0 | |||||||||||||||||||||
期刊ISSN | 0340-6717 | ![]() 蝌蝌APP,让您与同行交流更轻松
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E-ISSN | 1432-1203 | |||||||||||||||||||||
2024-2025最新影响因子 (数据来源于搜索引擎) | 3.6 点击查看影响因子趋势图 | |||||||||||||||||||||
实时影响因子 | 截止2025年5月19日:3.535 | |||||||||||||||||||||
2024-2025自引率 | 5.60%点击查看自引率趋势图 | |||||||||||||||||||||
五年影响因子 | 4.5 | |||||||||||||||||||||
JCI期刊引文指标 | 0.89 | |||||||||||||||||||||
h-index | 126 | |||||||||||||||||||||
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/439 | |||||||||||||||||||||
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/huge | |||||||||||||||||||||
作者指南网址 | https://www.springer.com/439/submission-guidelines | |||||||||||||||||||||
期刊语言要求 | Language Presenting your work in a well-structured manuscript and in well-written English gives it its best chance for editors and reviewers to understand it and evaluate it fairly. Many researchers find that getting some independent support helps them present their results in the best possible light. 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 GENETICS的语言要求,还能让HUMAN 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HUMAN 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 论文致谢 。 提交文稿 | |||||||||||||||||||||
是否OA开放访问 | No | |||||||||||||||||||||
通讯方式 | SPRINGER, 233 SPRING ST, NEW YORK, USA, NY, 10013 | |||||||||||||||||||||
出版商 | Springer Berlin Heidelberg | |||||||||||||||||||||
涉及的研究方向 | 生物-遗传学 | |||||||||||||||||||||
出版国家或地区 | UNITED STATES | |||||||||||||||||||||
出版语言 | English | |||||||||||||||||||||
出版周期 | Monthly | |||||||||||||||||||||
出版年份 | 1964 | |||||||||||||||||||||
年文章数 | 92点击查看年文章数趋势图 | |||||||||||||||||||||
Gold OA文章占比 | 42.47% | |||||||||||||||||||||
研究类文章占比: 文章 ÷(文章 + 综述) | 91.30% | |||||||||||||||||||||
WOS期刊SCI分区 ( 2024-2025年最新版) | WOS分区等级:2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SCI期刊分区 ( 2025年3月最新升级版) | 点击查看中国科学院SCI期刊分区趋势图
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中国科学院SCI期刊分区 ( 2023年12月升级版) |
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中国科学院SCI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) | |||||||||||||||||||||
PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0340-6717%5BISSN%5D | |||||||||||||||||||||
平均审稿速度 | 网友分享经验: 平均1月 | |||||||||||||||||||||
平均录用比例 | 网友分享经验: 约50% | |||||||||||||||||||||
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 GENETICS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. | Accelerating genetic diagnostics in retinitis pigmentosa: implementation of a semi-automated bespoke cohort analysis workflow for Hong Kong Genome Project Author: Ying, Dingge; Kwok, Jamie Sui Lam; Chu, Annie Tsz Wai; Ma, Wei; Tam, Helen Ying Fung; Or, Dicky; Hue, Shirley Pik Ying; Li, Qing; Leung, Christopher Kai Shun; Chung, Brian Hon Yin Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 5, pp. 515-528. DOI: 10.1007/s00439-025-02737-x PubMed DOI |
2. | Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain development Author: Chen, Bo; Zhang, Chenyang; Rui, Huanwen; Shen, Dan; Huang, Zhuxi; Feng, Weijun Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 5, pp. 529-543. DOI: 10.1007/s00439-025-02740-2 PubMed DOI |
3. | Comprehensive profiling of tsRNAs in acute coronary syndrome: expression patterns, clinical correlations, and functional insights Author: He, Yi; Wang, Jing; Chen, Chen; Wang, Rongli; Ma, Xiaozhu; Ma, Ruiying; Sun, Yang; Wang, Luyun; Ding, Hu Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 5, pp. 575-590. DOI: 10.1007/s00439-025-02742-0 PubMed DOI |
4. | Predicting the impact of rare variants on RNA splicing in CAGI6 Author: Lord, Jenny; Oquendo, Carolina Jaramillo; Wai, Htoo A.; Douglas, Andrew G. L.; Bunyan, David J.; Wang, Yaqiong; Hu, Zhiqiang; Zeng, Zishuo; Danis, Daniel; Katsonis, Panagiotis; Williams, Amanda; Lichtarge, Olivier; Chang, Yuchen; Bagnall, Richard D.; Mount, Stephen M.; Matthiasardottir, Brynja; Lin, Chiaofeng; Hansen, Thomas van Overeem; Leman, Raphael; Martins, Alexandra; Houdayer, Claude; Krieger, Sophie; Bakolitsa, Constantina; Peng, Yisu; Kamandula, Akash; Radivojac, Predrag; Baralle, Diana Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 2-3, pp. 243-251. DOI: 10.1007/s00439-023-02624-3 PubMed DOI |
5. | Decade-long application of preimplantation genetic testing for DMD/BMD: analysis of five clinical strategies and embryo recombination patterns Author: Wang, Weili; Dai, Jing; Hu, Xiao; He, Wenbin; Gu, Yifan; Wan, Zhenxing; Zhang, Yi; Luo, Keli; Li, Wen; Zhang, Qianjun; Gong, Fei; Lu, Guangxiu; Hu, Liang; Tan, Yue-Qiu; Lin, Ge; Du, Juan Journal: HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1007/s00439-025-02728-y PubMed DOI |
6. | Assessing the predicted impact of single amino acid substitutions in MAPK proteins for CAGI6 challenges Author: Turina, Paola; Petrosino, Maria; Enriquez Sandoval, Carlos A.; Novak, Leonore; Pasquo, Alessandra; Alexov, Emil; Alladin, Muttaqi Ahmad; Ascher, David B.; Babbi, Giulia; Bakolitsa, Constantina; Casadio, Rita; Cheng, Jianlin; Fariselli, Piero; Folkman, Lukas; Kamandula, Akash; Katsonis, Panagiotis; Li, Minghui; Li, Dong; Lichtarge, Olivier; Mahmud, Sajid; Martelli, Pier Luigi; Pal, Debnath; Panday, Shailesh Kumar; Pires, Douglas E. V.; Portelli, Stephanie; Pucci, Fabrizio; Rodrigues, Carlos H. M.; Rooman, Marianne; Savojardo, Castrense; Schwersensky, Martin; Shen, Yang; Strokach, Alexey V.; Sun, Yuanfei; Woo, Junwoo; Radivojac, Predrag; Brenner, Steven E.; Chiaraluce, Roberta; Consalvi, Valerio; Capriotti, Emidio Journal: HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1007/s00439-024-02724-8 PubMed DOI |
7. | CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs) Author: Aspromonte, Maria Cristina; Del Conte, Alessio; Zhu, Shaowen; Tan, Wuwei; Shen, Yang; Zhang, Yexian; Li, Qi; Wang, Maggie Haitian; Babbi, Giulia; Bovo, Samuele; Martelli, Pier Luigi; Casadio, Rita; Althagafi, Azza; Toonsi, Sumyyah; Kulmanov, Maxat; Hoehndorf, Robert; Katsonis, Panagiotis; Williams, Amanda; Lichtarge, Olivier; Xian, Su; Surento, Wesley; Pejaver, Vikas; Mooney, Sean D.; Sunderam, Uma; Srinivasan, Rajgopal; Murgia, Alessandra; Piovesan, Damiano; Tosatto, Silvio C. E.; Leonardi, Emanuela Journal: HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1007/s00439-024-02722-w PubMed DOI |
8. | Conventional and genetic association between migraine and stroke with druggable genome-wide Mendelian randomization Author: Wang, Xiaoyu; Pang, Wendu; Hu, Xin; Shu, Tao; Luo, Yaxin; Li, Junhong; Feng, Lan; Qiu, Ke; Rao, Yufang; Song, Yao; Mao, Minzi; Zhang, Yuyang; Ren, Jianjun; Zhao, Yu Journal: HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1007/s00439-024-02725-7 PubMed DOI |
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