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| 基本信息 | 登录收藏 | |||||||||||||||||||||
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期刊名字 | JOURNAL OF MEDICAL GENETICS J MED GENET （此期刊被最新的JCR期刊SCIE收录） LetPub评分 7.8
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声誉 8.8 影响力 6.6 速度 9.7 | |||||||||||||||||||||
| 期刊ISSN | 0022-2593 | 安装APP，查看期刊最新消息
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| E-ISSN | 1468-6244 | |||||||||||||||||||||
| 2025-2026最新IF （数据来源于网友提供） | 注册或登录后，查看IF | |||||||||||||||||||||
| 实时影响因子 | 截止2026年9月20日：1.851 | |||||||||||||||||||||
| 2025-2026自引率 | 0.0%点击查看自引率趋势图 | |||||||||||||||||||||
| 五年IF （数据来源于网友提供） | 3.795数据由网友[master_hawk]收集提供 | |||||||||||||||||||||
| h-index | 159 | |||||||||||||||||||||
| CiteScore （ 2026年6月最新版） |
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| 期刊简介 |
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| 期刊官方网站 | http://jmg.bmj.com/ | |||||||||||||||||||||
期刊投稿格式模板 VIP专享 |
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| 期刊投稿网址 | https://mc.manuscriptcentral.com/jmedgenet | |||||||||||||||||||||
| 该期刊中国学者近期发文 - New | Single-cell transcriptomics identifies neural fate disruption and glial reprogramming caused by RARS2 deficiency Author: Wei, Xing; Wang, Jing; Wang, Yanyun; Zhou, Cong; Chen, Zhaoyi; Liu, Shanling; Sun, Huaqin; Zhou, Bin; Zhang, Lin Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111413 CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders Author: Li, Yan-Fang; Mo, Pei; Zhang, Lan-Zhen; Zhou, Xin-Long; Zhu, Wen-Yu; Zhu, Jun-Hui; Liao, Shu-Hong; Chen, Ya-Ting; Deng, Weiwen; Zhang, Dong-Ming; Liu, Xiao-Rong; Chen, Yong-Jun; Liao, Wei-Ping; Wang, Jie; Cheng, Chuan-Fang Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-110918 Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank Author: Chen, Congcong; Zhu, Jiawen; Xu, Ziye; Gu, Xinyu; Shi, Yanan; Chen, Yingjia; Xie, Yuan; Yuan, Xin; Zhai, Qiqi; Zhou, Jun; Qin, Na; Dai, Juncheng; Ma, Hongxia; Jin, Guangfu; Shen, Hongbing; Hu, Zhibin; Wang, Cheng Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2026-111659 Functional characterisation and pathological significance of variants of MEF2C promoter in tetralogy of Fallot Author: Wang, Shao-Jie; Zheng, Zi-Fei; Chen, Huan-Xin; Yang, Qin; He, Guo-Wei Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2026-111657 | |||||||||||||||||||||
| 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JOURNAL OF MEDICAL GENETICS的语言要求，还能让JOURNAL OF MEDICAL 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 MEDICAL 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（1篇） 。
提交文稿 | |||||||||||||||||||||
| 是否OA开放访问 | No | |||||||||||||||||||||
| 通讯方式 | B M J PUBLISHING GROUP, BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON, ENGLAND, WC1H 9JR | |||||||||||||||||||||
| 出版商 | BMJ Publishing Group | |||||||||||||||||||||
| 涉及的研究方向 | 医学-遗传学 | |||||||||||||||||||||
| 出版国家或地区 | ENGLAND | |||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||
| 出版周期 | Monthly | |||||||||||||||||||||
| 出版年份 | 1964 | |||||||||||||||||||||
| 年文章数 | 112点击查看年文章数趋势图 | |||||||||||||||||||||
| Gold OA文章占比 | 33.33% | |||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 96.43% | |||||||||||||||||||||
| WOS期刊JCR分区 （ 2025-2026年最新版） | 注册或登录后，查看WOS分区等级 | |||||||||||||||||||||
| 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 | |||||||||||||||||||||
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| 《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=0022-2593%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： 一般 | |||||||||||||||||||||
| 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 MEDICAL GENETICS顺利发表。
快看看作者怎么说吧：服务好评 论文致谢（1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. | Single-cell transcriptomics identifies neural fate disruption and glial reprogramming caused by RARS2 deficiency Author: Wei, Xing; Wang, Jing; Wang, Yanyun; Zhou, Cong; Chen, Zhaoyi; Liu, Shanling; Sun, Huaqin; Zhou, Bin; Zhang, Lin Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111413 PubMed DOI |
| 2. | CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders Author: Li, Yan-Fang; Mo, Pei; Zhang, Lan-Zhen; Zhou, Xin-Long; Zhu, Wen-Yu; Zhu, Jun-Hui; Liao, Shu-Hong; Chen, Ya-Ting; Deng, Weiwen; Zhang, Dong-Ming; Liu, Xiao-Rong; Chen, Yong-Jun; Liao, Wei-Ping; Wang, Jie; Cheng, Chuan-Fang Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-110918 PubMed DOI |
| 3. | Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank Author: Chen, Congcong; Zhu, Jiawen; Xu, Ziye; Gu, Xinyu; Shi, Yanan; Chen, Yingjia; Xie, Yuan; Yuan, Xin; Zhai, Qiqi; Zhou, Jun; Qin, Na; Dai, Juncheng; Ma, Hongxia; Jin, Guangfu; Shen, Hongbing; Hu, Zhibin; Wang, Cheng Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2026-111659 PubMed DOI |
| 4. | Functional characterisation and pathological significance of variants of MEF2C promoter in tetralogy of Fallot Author: Wang, Shao-Jie; Zheng, Zi-Fei; Chen, Huan-Xin; Yang, Qin; He, Guo-Wei Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2026-111657 PubMed DOI |
| 5. | Frequent FBN2 variants in pectus excavatum highlight underlying phenotypic variability Author: Deng, Xicheng; Zheng, Yu; Wang, Jinghua; Shen, Fang; Luo, Jinwen; Liu, Cheng; Yang, Guihong; Yang, Yongjia Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2026-111615 PubMed DOI |
| 6. | Biallelic variants in DNAH10 are associated with skeletalf developmental abnormalities and ciliary dysfunction Author: Zheng, Rui; Du, Xinrong; Yan, Jierui; Huang, Gelin; Guo, Zhuoyao; Li, Wei; Que, Hanyun; Wen, Yuting; Yan, Fei; Chen, Daijuan; Dai, Li; Shi, Yu; Chen, Weicheng; Xu, Wenming Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111109 PubMed DOI |
| 7. | Updated ENIGMA recommendations for reporting germline variants in cancer susceptibility genes and their translation into twenty languages Author: De Nicolo, Arcangela; Eccles, Diana M.; Aaltonen, Kirsimari; Alhopuro, Pia; Ariansen, Sarah Louise; Biancolella, Michela; Caputo, Sandrine M.; Caron, Olivier; Cavalli, Pietro; Chiang, Jianbang; Claes, Kathleen B. M.; Cuaresma, Edgar Christian S.; de la Hoya, Miguel; De Pauw, Antoine; Diez, Orland; Dominguez-Valentin, Mev; Ehrencrona, Hans; Fjeldvaer, Magnhild K.; Fostira, Florentia; Francia, Marie Belle D.; Galego-Carro, Javier; Gomez Garcia, Encarna B.; Hassan, Nur Tiara; Hauke, Jan; Hirasawa, Akira; Huang, Xin; Ilagan-Cargullo, Elaine Marisse H.; Imoto, Issei; Jonnagadla, Sowmya; Karthikeyan, Manasadevi; Kleiblova, Petra; Konstantopoulou, Irene; Kowalik, Artur; Kvist, Anders; Lesueur, Fabienne; Li, Shao-Tzu; Lopez-Fernandez, Adria; Machackova, Eva; Martins, Alexandra; Mensenkamp, Arjen R.; Momozawa, Yukihide; Montalban, Gemma; Monteiro, Alvaro N. A.; Nevanlinna, Heli; Ngeow, Joanne; Palmero, Edenir Inez; Pedersen, Inge Sokilde; Que, Frances Victoria F.; Santamarina, Marta; Santana dos Santos, Elizabeth; Singer, Christian F.; Siolek, Monika; Solano, Angela R.; Soukupova, Jana; Suresh, Priyadharshin, I; Szczepaniak, Magdalena; Tan, Yen Y.; Teo, Soo Hwang; Tham, Emma; Thomassen, Mads; Tsaousis, Georgios; Hansen, Thomas van Overeem; Vega, Ana; Velasco-Sampedro, Eladio A.; Wangensteen, Teresia; Wappenschmidt, Barbara; Yannoukakos, Drakoulis; Yoon, Sook-Yee; Spurdle, Amanda B.; Radice, Paolo Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2026-111498 PubMed DOI |
| 8. | Expanded carrier screening in a Southwestern Chinese population indicates East Asian specific low-frequency pathogenic variants account for nearly half of the at-risk couple rate Author: Liu, Sha; Cao, Liyuan; Zhang, Victor Wei; Huang, Shuang; Liu, Haipeng; Wei, Xiang; Luo, Yuan; Li, Yue; Zhou, Lin; Jiang, Linzhi; Zhu, Qian; Liu, Hongqian Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111273 PubMed DOI |
| 9. | Clinical characteristics and prognosis of SDHD pathogenic variant carriers: a systematic review and meta-analysis Author: Lian, Xinquan; Shen, Liping; Song, Jiayin; Pang, Mengqi; Zhong, Yunmeng; Zhang, Han; Xing, Yadong; Tung, Tao-Hsin; Shen, Bo Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111235 PubMed DOI |
| 10. | Evaluating the efficiency of nanopore adaptive sampling sequencing in detecting balanced translocation Author: Gao, Meng; Ren, Jun; Peng, Cuiting; Liu, Xijing; Zheng, Jiemei; Chen, Han; Chen, Xinlian; Wang, Jiamin; Lai, Yi; Hu, Ting; Liu, Shanling Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111347 PubMed DOI |
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