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期刊名字 | CLINICAL GENETICS CLIN GENET （此期刊被最新的JCR期刊SCIE收录） LetPub评分 7.6
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声誉 8.8 影响力 6.3 速度 9.7 | |||||||||||||||||||||
| 期刊ISSN | 0009-9163 | 安装APP，查看期刊最新消息
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| E-ISSN | 1399-0004 | |||||||||||||||||||||
| 2024-2025最新影响因子 （数据来源于搜索引擎） | 2.3 点击查看影响因子趋势图 | |||||||||||||||||||||
| 实时影响因子 | 截止2026年5月06日：2.12 | |||||||||||||||||||||
| 2024-2025自引率 | 0.0%点击查看自引率趋势图 | |||||||||||||||||||||
| 五年影响因子 | 3.2 | |||||||||||||||||||||
| JCI期刊引文指标 | 0.63 | |||||||||||||||||||||
| h-index | 92 | |||||||||||||||||||||
| CiteScore （ 2025年最新版） |
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| 期刊简介 |
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| 期刊官方网站 | http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1399-0004 | |||||||||||||||||||||
期刊投稿格式模板 VIP专享 |
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| 期刊投稿网址 | http://mc.manuscriptcentral.com/cge | |||||||||||||||||||||
| 该期刊中国学者近期发文 - New | Ethnic Variation in G6PD Deficiency: Epidemiology and Mutation Spectrum in Southern China's Multiethnic Hub, Nanning Author: Yang, Jiawei; Li, Shengwei; Han, Yanfeng; Lei, Zixiao; Liao, Jiejun; Qiu, Yuling; Yang, Zheng Journal: CLINICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1111/cge.70144 WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes Author: Smith, Elyssa; Faundes, Victor; Zhao, Xiaonan; Zheng, Bixia; Zhang, Gang; Mao, Xiao; Danko, Emily; Laufman, Jason; Besnard, Thomas; Isidor, Bertrand; Cogne, Benjamin; Jensson, Brynjar Orn; Sulem, Telma S.; Sulem, Patrick; Rosenfeld, Jill A.; Scott, Daryl A Journal: CLINICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1111/cge.70160 Optic Atrophy Associated With a Mitochondrial G8363A Mutation in a Family Author: Lyu, Leyu; Sun, Xiaolei Journal: CLINICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1111/cge.70152 A Novel Compound Heterozygous Mutation in TEX14 Causes Human Non-Obstructive Azoospermia by Disrupting the Assembly of Intercellular Bridges Author: Li, Guotong; Zhou, Shushu; Li, Yuqian; Atta, Sana; Xia, Xun; Sha, Xuan; Hua, Rong; Zhou, Ping; Wei, Zhaolian; Cao, Yunxia; Wu, Huan Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14783 | |||||||||||||||||||||
| 期刊语言要求 | Language Manuscripts must be written in American English and be grammatically and linguistically correct. Authors should seek assistance with style, grammar and vocabulary if necessary. Your manuscript may also be sent back to you for revision if the quality of English language is poor. 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CLINICAL GENETICS的语言要求，还能让CLINICAL 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CLINICAL 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 | WILEY-BLACKWELL PUBLISHING, INC, COMMERCE PLACE, 350 MAIN ST, MALDEN, USA, MA, 02148 | |||||||||||||||||||||
| 出版商 | Wiley-Blackwell Publishing Ltd | |||||||||||||||||||||
| 涉及的研究方向 | 医学-遗传学 | |||||||||||||||||||||
| 出版国家或地区 | DENMARK | |||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||
| 出版周期 | Monthly | |||||||||||||||||||||
| 出版年份 | 1970 | |||||||||||||||||||||
| 年文章数 | 182点击查看年文章数趋势图 | |||||||||||||||||||||
| Gold OA文章占比 | 32.77% | |||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 89.56% | |||||||||||||||||||||
| WOS期刊JCR分区 （ 2024-2025年最新版） | WOS分区等级：3区
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| 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 | |||||||||||||||||||||
| 《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=0009-9163%5BISSN%5D | |||||||||||||||||||||
| 平均审稿速度 | 网友分享经验： 一般,3-8周 | |||||||||||||||||||||
| 平均录用比例 | 网友分享经验： 较易 | |||||||||||||||||||||
| 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CLINICAL 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. | Ethnic Variation in G6PD Deficiency: Epidemiology and Mutation Spectrum in Southern China's Multiethnic Hub, Nanning Author: Yang, Jiawei; Li, Shengwei; Han, Yanfeng; Lei, Zixiao; Liao, Jiejun; Qiu, Yuling; Yang, Zheng Journal: CLINICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1111/cge.70144 PubMed DOI |
| 2. | WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes Author: Smith, Elyssa; Faundes, Victor; Zhao, Xiaonan; Zheng, Bixia; Zhang, Gang; Mao, Xiao; Danko, Emily; Laufman, Jason; Besnard, Thomas; Isidor, Bertrand; Cogne, Benjamin; Jensson, Brynjar Orn; Sulem, Telma S.; Sulem, Patrick; Rosenfeld, Jill A.; Scott, Daryl A Journal: CLINICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1111/cge.70160 PubMed DOI |
| 3. | Optic Atrophy Associated With a Mitochondrial G8363A Mutation in a Family Author: Lyu, Leyu; Sun, Xiaolei Journal: CLINICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1111/cge.70152 PubMed DOI |
| 4. | A Novel Compound Heterozygous Mutation in TEX14 Causes Human Non-Obstructive Azoospermia by Disrupting the Assembly of Intercellular Bridges Author: Li, Guotong; Zhou, Shushu; Li, Yuqian; Atta, Sana; Xia, Xun; Sha, Xuan; Hua, Rong; Zhou, Ping; Wei, Zhaolian; Cao, Yunxia; Wu, Huan Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14783 PubMed DOI |
| 5. | Genetic Etiology of Epilepsy: A Retrospective Study From a Single-Center Cohort Author: Li, Yinchao; Xu, Xiaowei; She, Yingfang; Su, Zhengwei; Liu, Xianyue; Chen, Ying; Ye, Chenghui; Zhang, Yuanchao; Yu, Hang; Chen, Chun; Chen, Shuda; Zhou, Liemin Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14757 PubMed DOI |
| 6. | Identification of Shared Genetic Loci Associated With Inflammatory Bowel Disease, Ischemic Heart Disease, and Atrial Fibrillation and Flutter Author: Chen, Guojian; Luo, Qinghua; Wu, Chengcheng; Xie, Mingjun Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14749 PubMed DOI |
| 7. | Elucidating the Genetic Underpinnings of Human Musculoskeletal System Aging Through Genomic Structural Equation Modeling Author: Xiong, Hao; Shen, Pan; Luo, Qinghua; Zhang, Leichang; Li, Bo; Ding, Zhaohui; Wang, Lihua Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14766 PubMed DOI |
| 8. | Novel ABCD1 Variants in X-Linked Adrenoleukodystrophy Author: Dong, Sen-Wei; Xiao, Li-Mei; Sun, Yu-Hao; Li, Gui-He; Xie, Ying-Xuan; Wang, Meng-Wen; Wang, Ning; Chen, Wan-Jin; Chen, Hai-Zhu Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14752 PubMed DOI |
| 9. | Screening and Functional Analysis of TPO Gene Mutations in Patients With Congenital Hypothyroidism Author: Xu, Shiyi; Gao, Jiaying; Lin, Qiuting; Liu, Hui Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14754 PubMed DOI |
| 10. | Genetic Study and Prenatal Diagnosis of Inherited Glycosylphosphatidylinositol Disorders due to Novel Variants in Phosphatidylinositol Glycan Genes Author: Zhao, Zi-Xi; Zhou, Jing-Lin; Wang, Qi; Peng, Songmin; Peng, Yao; Wang, Yu-Rong; Hu, Liang; Aiyitahong, Rejima; Peng, Lin; Gu, Feng; Lu, Guang-Xiu; Lin, Ge; Chen, Song; Tan, Yue-Qiu; Du, Juan; He, Wen-Bin Journal: CLINICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1111/cge.14716 PubMed DOI |
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