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期刊名字 | HUMAN MOLECULAR GENETICS HUM MOL GENET （此期刊被最新的JCR期刊SCIE收录） LetPub评分 8.1
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声誉 8.8 影响力 7.1 速度 9.5 | |||||||||||||||||||||||||||||||
| 期刊ISSN | 0964-6906 | 
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| E-ISSN | 1460-2083 | |||||||||||||||||||||||||||||||
| 2024-2025最新影响因子 （数据来源于搜索引擎） | 3.2 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：2.32 | |||||||||||||||||||||||||||||||
| 2024-2025自引率 | 0.0%点击查看自引率趋势图 | |||||||||||||||||||||||||||||||
| 五年影响因子 | 3.8 | |||||||||||||||||||||||||||||||
| JCI期刊引文指标 | 0.8 | |||||||||||||||||||||||||||||||
| h-index | 255 | |||||||||||||||||||||||||||||||
| 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://academic.oup.com/hmg | |||||||||||||||||||||||||||||||
期刊投稿格式模板 VIP专享 |
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| 期刊投稿网址 | http://www.oxfordjournals.org/our_journals/hmg/for_authors/submission_online.html | |||||||||||||||||||||||||||||||
| 该期刊中国学者近期发文 - New | COQ8B gene deficiency as a potential cause of retinal abnormalities in Pediatric kidney transplant recipients Author: Feng, Yonghua; Feng, Yi; Wang, Zhigang; Li, Wenjing; Zhu, Haowei; Li, Zhou; Feng, Chenghao; Xu, Hongen; Feng, Guiwen; Zhang, Di; Shang, Wenjun Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf084 De novo missense variants of KCNA3, KCNA4, and KCNA6 cause early onset developmental epileptic encephalopathy Author: Tsai, Meng-Han; Lo, Chia-Hua; Liu, You-Xuan; Wu, Sheng-Nan; Kuo, Cheng-Yen; Liu, Yi-Hsuan; Chang, Ying-Chao; Lin, Kuan-Lin; Hung, Po-Cheng; Chen, Hwei-Hsien; Chen, Jian-Liang; Yao, Chi-Kuang; Hwang, Eric; Wang, Ya-Jean Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf090 Calcium homeostasis modulator 2 aggravates α-synuclein-induced neurotoxicity in Parkinson's disease by activating PARP-1 depended Parthanatos Author: Pan, Qi; Xu, Huanjun; Xiao, Zongyu; Liu, Guanghao; Zhang, Huaming; Li, Yiying Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf091 Linking DNA methylation in brain regions to Alzheimer's disease risk: a Mendelian randomization study Author: Zhong, Hua; Zhu, Jingjing; Liu, Shuai; Zhou, Dan; Long, Quan; Wu, Chong; Zhao, Bingxin; Cheng, Chao; Yang, Yaohua; Wu, Qing; Wu, Yong; Li, Changwei; Wang, Zhaoming; Wu, Jianyong; Guo, Xingyi; Zhi, Degui; Deng, Youping; Wu, Lang Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf053 | |||||||||||||||||||||||||||||||
| 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 MOLECULAR GENETICS的语言要求，还能让HUMAN MOLECULAR 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 MOLECULAR 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 | OXFORD UNIV PRESS, GREAT CLARENDON ST, OXFORD, ENGLAND, OX2 6DP | |||||||||||||||||||||||||||||||
| 出版商 | Oxford University Press | |||||||||||||||||||||||||||||||
| 涉及的研究方向 | 生物-生化与分子生物学 | |||||||||||||||||||||||||||||||
| 出版国家或地区 | ENGLAND | |||||||||||||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||||||||||||
| 出版周期 | Semimonthly | |||||||||||||||||||||||||||||||
| 出版年份 | 1992 | |||||||||||||||||||||||||||||||
| 年文章数 | 171点击查看年文章数趋势图 | |||||||||||||||||||||||||||||||
| Gold OA文章占比 | 35.83% | |||||||||||||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 91.81% | |||||||||||||||||||||||||||||||
| WOS期刊JCR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) | |||||||||||||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0964-6906%5BISSN%5D | |||||||||||||||||||||||||||||||
| 平均审稿速度 | 网友分享经验： 较快,2-4周 | |||||||||||||||||||||||||||||||
| 平均录用比例 | 网友分享经验： 较难 | |||||||||||||||||||||||||||||||
| 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 MOLECULAR 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. | COQ8B gene deficiency as a potential cause of retinal abnormalities in Pediatric kidney transplant recipients Author: Feng, Yonghua; Feng, Yi; Wang, Zhigang; Li, Wenjing; Zhu, Haowei; Li, Zhou; Feng, Chenghao; Xu, Hongen; Feng, Guiwen; Zhang, Di; Shang, Wenjun Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf084 PubMed DOI |
| 2. | De novo missense variants of KCNA3, KCNA4, and KCNA6 cause early onset developmental epileptic encephalopathy Author: Tsai, Meng-Han; Lo, Chia-Hua; Liu, You-Xuan; Wu, Sheng-Nan; Kuo, Cheng-Yen; Liu, Yi-Hsuan; Chang, Ying-Chao; Lin, Kuan-Lin; Hung, Po-Cheng; Chen, Hwei-Hsien; Chen, Jian-Liang; Yao, Chi-Kuang; Hwang, Eric; Wang, Ya-Jean Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf090 PubMed DOI |
| 3. | Calcium homeostasis modulator 2 aggravates α-synuclein-induced neurotoxicity in Parkinson's disease by activating PARP-1 depended Parthanatos Author: Pan, Qi; Xu, Huanjun; Xiao, Zongyu; Liu, Guanghao; Zhang, Huaming; Li, Yiying Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf091 PubMed DOI |
| 4. | Linking DNA methylation in brain regions to Alzheimer's disease risk: a Mendelian randomization study Author: Zhong, Hua; Zhu, Jingjing; Liu, Shuai; Zhou, Dan; Long, Quan; Wu, Chong; Zhao, Bingxin; Cheng, Chao; Yang, Yaohua; Wu, Qing; Wu, Yong; Li, Changwei; Wang, Zhaoming; Wu, Jianyong; Guo, Xingyi; Zhi, Degui; Deng, Youping; Wu, Lang Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf053 PubMed DOI |
| 5. | Genetic characteristics associated with isolated Microtia revealed through whole exome sequencing of 201 pedigrees Author: Wu, Siyi; Chen, Xin; Chen, Ying; Li, Chenlong; Yang, Run; Zhang, Tianyu; Ma, Jing Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf063 PubMed DOI |
| 6. | Loss of Nup160 dysregulates Cdc42 in the podocytes of podocyte-specific Nup160 knockout mice Author: Liu, Deying; Li, Jiaxin; Xu, Chan; Li, Yuanyuan; Chen, Xiaohan; Zhao, Feng; Tong, Huajuan; Yang, Yonghui; Qiu, Xiaojian; Yu, Zihua Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf064 PubMed DOI |
| 7. | Single-cell transcriptome unveils mesenchymal cell diversity in endometriosis Author: Chen, Xia; Zhang, Shengkun; Qi, Yujuan; Wu, Tiantian; Huang, Qiuru; Bao, Xueyun; Gu, Juan; Sun, Qingqing; Shao, Yueyue; Jiang, Nan; Chen, Ning; Li, Zhenbei; Zheng, Sen; Cao, Xiangnan; Li, Jiaxin; Zheng, Bo; Shi, Zhonghua; Cao, Yijuan; Sun, Xiaoli; Yu, Jun Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf065 PubMed DOI |
| 8. | Genome-wide association study for lung cancer in 6531 African Americans reveals new susceptibility loci Author: Byun, Jinyoung; Han, Younghun; Choi, Jiyeon; Sun, Ryan; Shaw, Vikram R.; Zhu, Catherine; Xiao, Xiangjun; Lusk, Christine; Badr, Hoda; Lee, Hyun-Sung; Jang, Hee-Jin; Li, Yafang; Lim, Hyeyeun; Long, Erping; Liu, Yanhong; Kachuri, Linda; Walsh, Kyle M.; Wiencke, John K.; Albanes, Demetrius; Lam, Stephen; Tardon, Adonina; Neuhouser, Marian L.; Barnett, Matt J.; Chen, Chu; Bojesen, Stig; Brenner, Hermann; Landi, Maria Teresa; Johansson, Mattias; Risch, Angela; Wichmann, H-Erich; Bickeboeller, Heike; Christiani, David C.; Rennert, Gad; Arnold, Susanne; Field, John K.; Shete, Sanjay; Le Marchand, Loic; Liu, Geoffrey; Andrew, Angeline S.; Zienolddiny, Shanbeh; Grankvist, Kjell; Johansson, Mikael; Caporaso, Neil; Taylor, Fiona; Lazarus, Philip; Schabath, Matthew B.; Aldrich, Melinda C.; Patel, Alpa; Lin, Xihong; Zanetti, Krista A.; Harris, Curtis C.; Chanock, Stephen; Mckay, James; Schwartz, Ann G.; Hung, Rayjean J.; Amos, Christopher, I Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf059 PubMed DOI |
| 9. | Whole-exome sequencing identifies 5 novel genes associated with carpal tunnel syndrome Author: Wang, Zi-Yi; He, Xiao-Yu; Wu, Bang-Sheng; Yang, Liu; You, Jia; Liu, Wei-Shi; Feng, Jian-Feng; Cheng, Wei; Yu, Jin-Tai Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf076 PubMed DOI |
| 10. | The p.W651fsX666 mutation on COL10A1 results in impaired trimerization of normal collagen X to induce Schmid type Metaphyseal chondrodysplasia Author: Yang, Jingye; Zhang, Jing; Lu, Qingxiang; Tian, Haiying; Wang, Ke; Liu, Zhi; Xiong, Yu; Li, Yadong; Ma, Ning; Tian, Hongxia; Zhou, Zhongxue; Zhou, Ding'an Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf071 PubMed DOI |
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