2023年6月最新SCI影响因子数据已经更新,欢迎查询! 如果您对期刊系统有任何需求或者问题,欢迎
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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 | 微信扫码收藏此期刊 | ||||||||||||||||||||
E-ISSN | 1468-6244 | |||||||||||||||||||||
2022-2023最新影响因子 (数据来源于搜索引擎) | 4 点击查看影响因子趋势图 | |||||||||||||||||||||
实时影响因子 | 截止2023年9月27日:2.23 | |||||||||||||||||||||
2022-2023自引率 | 2.50%点击查看自引率趋势图 | |||||||||||||||||||||
五年影响因子 | 4.9 | |||||||||||||||||||||
h-index | 159 | |||||||||||||||||||||
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期刊简介 | Journal of Medical Genetics is a leading international peer-reviewed journal covering original research in human genetics, including reviews of and opinion on the latest developments. Articles cover the molecular basis of human disease including germline cancer genetics, clinical manifestations of genetic disorders, applications of molecular genetics to medical practice and the systematic evaluation of such applications worldwide. | |||||||||||||||||||||
期刊官方网站 | http://jmg.bmj.com/ | |||||||||||||||||||||
期刊投稿网址 | https://mc.manuscriptcentral.com/jmedgenet | |||||||||||||||||||||
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 。
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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 | 134点击查看年文章数趋势图 | |||||||||||||||||||||
Gold OA文章占比 | 34.77% | |||||||||||||||||||||
研究类文章占比: 文章 ÷(文章 + 综述) | 94.78% | |||||||||||||||||||||
WOS期刊SCI分区 ( 2022-2023年最新版) | WOS分区等级:2区
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中科院《国际期刊预警 名单(试行)》名单 | 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 2021年01月发布的2020版:不在预警名单中 | |||||||||||||||||||||
中科院SCI期刊分区 ( 2022年12月最新升级版) | 点击查看中科院SCI期刊分区趋势图
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中科院SCI期刊分区 ( 2021年12月基础版) |
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中科院SCI期刊分区 ( 2021年12月升级版) |
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中科院SCI期刊分区 ( 2020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 | |||||||||||||||||||||
期刊常用信息链接 |
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中国学者近期发表的论文 | |
1. | Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility Author: Liu, Chunyu; Shen, Ying; Tang, Shuyan; Wang, Jiaxiong; Zhou, Yiling; Tian, Shixiong; Wu, Huan; Cong, Jiangshan; He, Xiaojin; Jin, Li; Cao, Yunxia; Yang, Yihong; Zhang, Feng Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. 60, Issue 2, pp. 137-143. DOI: 10.1136/jmedgenet-2021-108271 PubMed DOI |
2. | Novel truncating variants in CTNNB1 cause familial exudative vitreoretinopathy Author: He, Yunqi; Yang, Mu; Zhao, Rulian; Peng, Li; Dai, Erkuan; Huang, Lulin; Zhao, Peiquan; Li, Shujin; Yang, Zhenglin Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. 60, Issue 2, pp. 174-182. DOI: 10.1136/jmedgenet-2021-108259 PubMed DOI |
3. | Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia Author: Hu, Tongyao; Meng, Lanlan; Tan, Chen; Luo, Chen; He, Wen-Bin; Tu, Chaofeng; Zhang, Huan; Du, Juan; Nie, Hongchuan; Lu, Guang-Xiu; Lin, Ge; Tan, Yue-Qiu Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. 60, Issue 2, pp. 144-153. DOI: 10.1136/jmedgenet-2021-108249 PubMed DOI |
4. | GLRA2 gene mutations cause high myopia in humans and mice Author: Tian, Qi; Tong, Ping; Chen, Gong; Deng, Meichun; Cai, Tian'e; Tian, Runyi; Zhang, Zimin; Xia, Kun; Hu, Zhengmao Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. 60, Issue 2, pp. 193-203. DOI: 10.1136/jmedgenet-2022-108425 PubMed DOI |
5. | Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice Author: Liu, Wensheng; Wei, Xiaoli; Liu, Xiaoyan; Chen, Gaowen; Zhang, Xiaoya; Liang, Xiaomei; Isachenko, Vladimir; Sha, Yanwei; Wang, Yifeng Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. 60, Issue 2, pp. 154-162. DOI: 10.1136/jmedgenet-2021-108137 PubMed DOI |
6. | Genotype-phenotype correlations and clinical outcomes of patients with von Hippel-Lindau disease with large deletions Author: Zhang, Kenan; Yang, Wuping; Ma, Kaifang; Qiu, Jianhui; Li, Lei; Xu, Yawei; Zhang, Zedan; Yu, Chaojian; Zhou, Jingcheng; Gong, Yanqing; Cai, Lin; Gong, Kan Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. 60, Issue 5, pp. 477-483. DOI: 10.1136/jmg-2022-108633 PubMed DOI |
7. | Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA Author: Tian, Shixiong; Tu, Chaofeng; He, Xiaojin; Meng, Lanlan; Wang, Jiaxiong; Tang, Shuyan; Gao, Yang; Liu, Chunyu; Wu, Huan; Zhou, Yiling; Lv, Mingrong; Lin, Ge; Jin, Li; Cao, Yunxia; Tang, Dongdong; Zhang, Feng; Tan, Yue-Qiu Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2022-108887 PubMed DOI |
8. | Clinical and genetic features of GATOR1 complex-associated epilepsy Author: Yin, Kaili; Lei, Xingxing; Yan, Zhaofen; Yang, Yujiao; Deng, Qinqin; Lu, Qiang; Zhang, Xue; Wang, Mengyang; Liu, Qing Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2021-108364 PubMed DOI |
9. | Profiling of the genetic features of Chinese patients with gastric cancer with HRD germline mutations in a large-scale retrospective study Author: Zhang, Chenghai; Zhu, Dandan; Qu, Yurong; Shi, Min; Ma, Jingjiao; Peng, Yebo; Zhu, Bowen; Tao, Houquan; Ma, Tonghui; Hou, TieYing Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2022-108816 PubMed DOI |
10. | Parental mosaicism detection and preimplantation genetic testing in families with multiple transmissions of de novo mutations Author: Xu, Naixin; Shi, Weihui; Cao, Xianling; Zhou, Xuanyou; Jin, Li; Huang, He-Feng; Chen, Songchang; Xu, Chenming Journal: JOURNAL OF MEDICAL GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2022-108920 PubMed DOI |
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