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| 基本信息 | 登录收藏 | |||||||||||||||||||||
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期刊名字 | JOURNAL OF HUMAN GENETICS J HUM GENET （此期刊被最新的JCR期刊SCIE收录） LetPub评分 6.5
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声誉 7.5 影响力 5.2 速度 9.1 | |||||||||||||||||||||
| 期刊ISSN | 1434-5161 | 微信扫码收藏此期刊 | ||||||||||||||||||||
| E-ISSN | 1435-232X | |||||||||||||||||||||
| 2023-2024最新影响因子 （数据来源于搜索引擎） | 2.6 点击查看影响因子趋势图 | |||||||||||||||||||||
| 实时影响因子 | 截止2024年10月29日：1.817 | |||||||||||||||||||||
| 2023-2024自引率 | 3.80%点击查看自引率趋势图 | |||||||||||||||||||||
| 五年影响因子 | 2.6 | |||||||||||||||||||||
| JCI期刊引文指标 | 0.77 | |||||||||||||||||||||
| h-index | 75 | |||||||||||||||||||||
| CiteScore （ 2024年最新版） |
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| 期刊简介 |
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| 期刊官方网站 | https://www.nature.com/jhg | |||||||||||||||||||||
| 期刊投稿网址 | https://www.springer.com/12508 | |||||||||||||||||||||
| 作者指南网址 | https://www.nature.com/jhg/authors-and-referees | |||||||||||||||||||||
| 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JOURNAL OF HUMAN GENETICS的语言要求，还能让JOURNAL OF 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JOURNAL OF 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 备注：Archive content is freely available after five years. | |||||||||||||||||||||
| 通讯方式 | NATURE PUBLISHING GROUP, 75 VARICK ST, 9TH FLR, NEW YORK, USA, NY, 10013-1917 | |||||||||||||||||||||
| 出版商 | Springer Nature | |||||||||||||||||||||
| 涉及的研究方向 | 生物-遗传学 | |||||||||||||||||||||
| 出版国家或地区 | JAPAN | |||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||
| 出版周期 | Monthly | |||||||||||||||||||||
| 出版年份 | 1977 | |||||||||||||||||||||
| 年文章数 | 92点击查看年文章数趋势图 | |||||||||||||||||||||
| Gold OA文章占比 | 19.93% | |||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 97.83% | |||||||||||||||||||||
| WOS期刊SCI分区 （ 2023-2024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 | 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 （ 2023年12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 （ 2022年12月升级版） |
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| 中国科学院SCI期刊分区 （ 2021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=1434-5161%5BISSN%5D | |||||||||||||||||||||
| 平均审稿速度 | 网友分享经验： 偏慢,4-8周 | |||||||||||||||||||||
| 平均录用比例 | 网友分享经验： 容易 | |||||||||||||||||||||
| 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JOURNAL OF HUMAN GENETICS顺利发表。
快看看作者怎么说吧：服务好评 论文致谢 | |||||||||||||||||||||
| 期刊常用信息链接 |
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| 中国学者近期发表的论文 | |
| 1. | Concurrence of novel mutations causing Gilbert's and Dubin-Johnson syndrome with poor clinical outcomes in a Han Chinese family Author: Zhou, Tai-Cheng; Li, Xiao; Li, Hui; Liu, Feng-Wei; Zhang, Si-Hang; Fan, Jing-Hua; Yang, Wen-Xiu; Yang, Ya-Li; Zhang, Liang; Wei, Jia Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. 68, Issue 1, pp. 17-23. DOI: 10.1038/s10038-022-01086-1 PubMed DOI |
| 2. | Mendelian randomization study on the causal effects of systemic lupus erythematosus on major depressive disorder Author: Li, Wenchang; Kan, Hoktim; Zhang, Weizhe; Zhong, Yanlin; Liao, Weiming; Huang, Guiwu; Wu, Peihui Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. 68, Issue 1, pp. 11-16. DOI: 10.1038/s10038-022-01080-7 PubMed DOI |
| 3. | Exon skipping caused by splicing mutation in TNNT1 nemaline myopathy Author: Wang, Guangyu; Zhao, Dandan; Yan, Chuanzhu; Lin, Pengfei Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. 68, Issue 2, pp. 97-101. DOI: 10.1038/s10038-022-01096-z PubMed DOI |
| 4. | Analyzing the effects of BRCA1/2 variants on mRNA splicing by minigene assay Author: Dong, Zhouhuan; Wang, Yun; Zhang, Jing; Zhu, Fengwei; Liu, Zhiyuan; Kang, Yajun; Lin, Mingyuan; Shi, Huaiyin Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. 68, Issue 2, pp. 65-71. DOI: 10.1038/s10038-022-01077-2 PubMed DOI |
| 5. | Detecting genomic mosaicism in de novo genetic epilepsy by amplicon-based deep sequencing Author: Chen, Jiaoyang; Chen, Yi; Yang, Ying; Niu, Xueyang; Zhang, Jing; Zeng, Qi; Liu, Aijie; Xu, Xiaojing; Yang, Xiaoxu; Li, Shupin; Yang, Xiaoling; Wang, Yi; Zhang, Yuehua Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. 68, Issue 2, pp. 73-80. DOI: 10.1038/s10038-022-01103-3 PubMed DOI |
| 6. | PSMC6 induces immune cell infiltration and inflammatory response to aggravate primary Sjogren's syndrome Author: Piao, Yongzhu; Qi, Yutong; Zhang, Hao; Han, Longyin; Zhong, Xiayuan; Liu, Qingnan Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1038/s10038-022-01107-z PubMed DOI |
| 7. | Illuminating the potential causality of serum level of matrix metalloproteinases and the occurrence of cardiovascular and cerebrovascular diseases: a Mendelian randomization study Author: Zou, Xuelun; Wang, Leiyun; Zeng, Yi; Zhang, Le Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1038/s10038-023-01154-0 PubMed DOI |
| 8. | A presumed missense variant in the U2AF2 gene causes exon skipping in neurodevelopmental diseases Author: Wang, Xiaole; You, Baiyang; Yin, Fei; Chen, Chen; He, Hailan; Liu, Fangyun; Pan, Zou; Ni, Xiaoyuan; Pang, Nan; Peng, Jing Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1038/s10038-023-01128-2 PubMed DOI |
| 9. | Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia Author: Zhang, Yuxiang; Li, Na; Ji, Zhiyong; Bai, Haowei; Ou, Ningjing; Tian, Ruhui; Li, Peng; Zhi, Erlei; Huang, Yuhua; Zhao, Jingpeng; Han, Yaqin; Zhang, Jing; Zhou, Yuchuan; Li, Zheng; Yao, Chencheng Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1038/s10038-023-01119-3 PubMed DOI |
| 10. | Association of MPPED2 gene variant rs10767873 with kidney function and risk of cardiovascular disease in patients with hypertension Author: Zhong, Yixuan; Wu, Yiyi; Yang, Yunyun; Chen, Yu; Hui, Rutai; Zhang, Mei; Zhang, Weili Journal: JOURNAL OF HUMAN GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1038/s10038-022-01118-w PubMed DOI |
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