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期刊名字 | HUMAN GENETICS HUM GENET (此期刊被最新的JCR期刊SCIE收录) LetPub评分 7.7
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声誉 8.8 影响力 6.6 速度 9.2 | |||||||||||||||||||||
期刊ISSN | 0340-6717 | 微信扫码收藏此期刊 | ||||||||||||||||||||
E-ISSN | 1432-1203 | |||||||||||||||||||||
2022-2023最新影响因子 (数据来源于搜索引擎) | 5.3 点击查看影响因子趋势图 | |||||||||||||||||||||
实时影响因子 | 截止2023年12月27日:3.566 | |||||||||||||||||||||
2022-2023自引率 | 3.80%点击查看自引率趋势图 | |||||||||||||||||||||
五年影响因子 | 5.2 | |||||||||||||||||||||
h-index | 126 | |||||||||||||||||||||
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期刊简介 | Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted. The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder. | |||||||||||||||||||||
期刊官方网站 | https://www.springer.com/439 | |||||||||||||||||||||
期刊投稿网址 | https://www.editorialmanager.com/huge | |||||||||||||||||||||
作者指南网址 | https://www.springer.com/439/submission-guidelines | |||||||||||||||||||||
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HUMAN GENETICS的语言要求,还能让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 | |||||||||||||||||||||
通讯方式 | SPRINGER, 233 SPRING ST, NEW YORK, USA, NY, 10013 | |||||||||||||||||||||
出版商 | Springer Berlin Heidelberg | |||||||||||||||||||||
涉及的研究方向 | 生物-遗传学 | |||||||||||||||||||||
出版国家或地区 | UNITED STATES | |||||||||||||||||||||
出版语言 | English | |||||||||||||||||||||
出版周期 | Monthly | |||||||||||||||||||||
出版年份 | 1964 | |||||||||||||||||||||
年文章数 | 94点击查看年文章数趋势图 | |||||||||||||||||||||
Gold OA文章占比 | 30.30% | |||||||||||||||||||||
研究类文章占比: 文章 ÷(文章 + 综述) | 85.11% | |||||||||||||||||||||
WOS期刊SCI分区 ( 2022-2023年最新版) | WOS分区等级:1区
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中科院《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 | |||||||||||||||||||||
中科院SCI期刊分区 ( 2023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 ( 2022年12月升级版) |
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中科院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=0340-6717%5BISSN%5D | |||||||||||||||||||||
平均审稿速度 | 网友分享经验: 平均1月 | |||||||||||||||||||||
平均录用比例 | 网友分享经验: 约50% | |||||||||||||||||||||
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 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. | Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss Author: Xiang, Jiale; Sun, Xiangzhong; Song, Nana; Ramaswamy, Sathishkumar; Abou Tayoun, Ahmad N.; Peng, Zhiyu Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 33-43. DOI: 10.1007/s00439-022-02479-0 PubMed DOI |
2. | Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformation Author: Liu, Zhenlei; Du, Huakang; Zhao, Hengqiang; Cai, Siyi; Zhao, Sen; Niu, Yuchen; Li, Xiaoxin; Liu, Bowen; Huang, Yingzhao; Shao, Jiashen; Liu, Lian; Tian, Ye; Wu, Zhihong; Wu, Hao; Hu, Yue; Zhang, Terry Jianguo; Jian, Fengzeng; Wu, Nan Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 89-101. DOI: 10.1007/s00439-022-02474-5 PubMed DOI |
3. | Truncation mutations in MYRF underlie primary angle closure glaucoma Author: Ouyang, Jiamin; Sun, Wenmin; Shen, Huangxuan; Liu, Xing; Wu, Yingchen; Jiang, Hongmei; Li, Xueqing; Wang, Yingwei; Jiang, Yi; Li, Shiqiang; Xiao, Xueshan; Hejtmancik, J. Fielding; Tan, Zhiqun; Zhang, Qingjiong Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 103-123. DOI: 10.1007/s00439-022-02487-0 PubMed DOI |
4. | Common genetic risk factors in ASD and ADHD co-occurring families Author: Zhou, Anbo; Cao, Xiaolong; Mahaganapathy, Vaidhyanathan; Azaro, Marco; Gwin, Christine; Wilson, Sherri; Buyske, Steven; Bartlett, Christopher W.; Flax, Judy F.; Brzustowicz, Linda M.; Xing, Jinchuan Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 217-230. DOI: 10.1007/s00439-022-02496-z PubMed DOI |
5. | Profiling human pathogenic repeat expansion regions by synergistic and multi-level impacts on molecular connections Author: Fan, Cong; Chen, Ken; Wang, Yukai; Ball, Edward, V; Stenson, Peter D.; Mort, Matthew; Bacolla, Albino; Kehrer-Sawatzki, Hildegard; Tainer, John A.; Cooper, David N.; Zhao, Huiying Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 245-274. DOI: 10.1007/s00439-022-02500-6 PubMed DOI |
6. | Identifying shared genetic factors underlying epilepsy and congenital heart disease in Europeans Author: Wu, Yiming; Bayrak, Cigdem Sevim; Dong, Bosi; He, Shixu; Stenson, Peter D.; Cooper, David N.; Itan, Yuval; Chen, Lei Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 275-288. DOI: 10.1007/s00439-022-02502-4 PubMed DOI |
7. | Variations in mitochondrial DNA coding and d-loop region are associated with early embryonic development defects in infertile women Author: Liu, Yuqing; Zhao, Shuai; Chen, Xiaolei; Bian, Yuehong; Cao, Yongzhi; Xu, Peiwen; Zhang, Changming; Zhang, Jiangtao; Zhao, Shigang; Zhao, Han Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 193-200. DOI: 10.1007/s00439-022-02505-1 PubMed DOI |
8. | Hearing of Otof-deficient mice restored by trans-splicing of N- and C-terminal otoferlin Author: Tang, Honghai; Wang, Hui; Wang, Shengyi; Hu, Shao Wei; Lv, Jun; Xun, Mengzhao; Gao, Kaiyu; Wang, Fang; Chen, Yuxin; Wang, Daqi; Wang, Wuqing; Li, Huawei; Shu, Yilai Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 289-304. DOI: 10.1007/s00439-022-02504-2 PubMed DOI |
9. | Investigating the shared genetic architecture and causal relationship between pain and neuropsychiatric disorders Author: Chen, Mengya; Li, Si; Zhu, Ziwei; Dai, Chengguqiu; Hao, Xingjie Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 3, pp. 431-443. DOI: 10.1007/s00439-022-02507-z PubMed DOI |
10. | Proteome-wide Mendelian randomization reveals the causal effects of immune-related plasma proteins on psychiatric disorders Author: Dang, Xinglun; Song, Meng; Lv, Luxian; Yang, Yongfeng; Luo, Xiong-Jian Journal: HUMAN GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1007/s00439-023-02562-0 PubMed DOI |
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