缩写名/全名 |
HUM GENET
HUMAN GENETICS |
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ISSN号 | 0340-6717 | ||||||||||||||||||||
研究方向 | 生物-遗传学 | ||||||||||||||||||||
影响因子 | 2015:5.138, 2016:4.637, 2017:3.93, 2018:5.207, 2019:5.743, | ||||||||||||||||||||
出版国家 | UNITED STATES | ||||||||||||||||||||
出版周期 | Monthly | ||||||||||||||||||||
年文章数 | 108 | ||||||||||||||||||||
出版年份 | 1976 | ||||||||||||||||||||
是否OA | No | ||||||||||||||||||||
审稿周期(仅供参考) | 平均1月 |
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录用比例 | 约50% | ||||||||||||||||||||
投稿链接 | https://www.editorialmanager.com/huge/default.aspx | ||||||||||||||||||||
投稿官网 | http://link.springer.com/journal/439 | ||||||||||||||||||||
h-index | 126 | ||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0340-6717%5BISSN%5D | ||||||||||||||||||||
中科院SCI期刊分区 ( 2018年新版本) |
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中科院SCI期刊分区 ( 2020年新版本) |
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中国学者近期发表的论文 | |
1. | Novel mutations in <Emphasis Type="Italic">ZP1, ZP2</Emphasis>, and <Emphasis Type="Italic">ZP3</Emphasis> cause female infertility due to abnormal zona pellucida formation Author: Zhou Zhou, Caixia Ni, Ling Wu, Biaobang Chen, Yao Xu, Zhihua Zhang, Jian Mu, Bin Li, Zheng Yan, Jing Fu, Wenjing Wang, Lin Zhao, Jie Dong, Xiaoxi Sun, Yanping Kuang, Qing Sang, Lei Wang Journal: HUMAN GENETICS, 2019, Vol., , DOI:10.1007/s00439-019-01990-1 DOI |
2. | LncRNA ZBTB40-IT1 modulated by osteoporosis GWAS risk SNPs suppresses osteogenesis Author: Bing Mei, Ya Wang, Weiyuan Ye, Han Huang, Qian Zhou, Yuanyuan Chen, Yajing Niu, Manling Zhang, Qingyang Huang Journal: HUMAN GENETICS, 2019, Vol., , DOI:10.1007/s00439-019-01969-y DOI |
3. | Whole-exome sequencing reveals <Emphasis Type="Italic">SALL4</Emphasis> variants in premature ovarian insufficiency: an update on genotype–phenotype correlations Author: Qiqi Wang, Da Li, Baozhu Cai, Qing Chen, Caihua Li, Yanhua Wu, Li Jin, Xiuxia Wang, Xiaojin Zhang, Feng Zhang Journal: HUMAN GENETICS, 2019, Vol., , DOI:10.1007/s00439-018-1962-4 DOI |
4. | A novel method for identifying nonlinear gene–environment interactions in case–control association studies Author: Cen Wu, Yuehua Cui Journal: HUMAN GENETICS, 2013, Vol.132, 1413-1425, DOI:10.1007/s00439-013-1350-z DOI |
5. | Comprehensively identifying and characterizing the missing gene sequences in human reference genome with integrated analytic approaches Author: Geng Chen, Charles Wang, Leming Shi, Weida Tong, Xiongfei Qu, Jiwei Chen, Jianmin Yang, Caiping Shi, Long Chen, Peiying Zhou, Bingxin Lu, Tieliu Shi Journal: HUMAN GENETICS, 2013, Vol.132, 899-911, DOI:10.1007/s00439-013-1300-9 DOI |
6. | Synergistical effect of 20-HETE and high salt on NKCC2 protein and blood pressure via ubiquitin–proteasome pathway Author: Jingjing Wu, Xiaoliang Liu, Guangrui Lai, Xianghong Yang, Luzeng Wang, Yanyan Zhao Journal: HUMAN GENETICS, 2012, Vol.132, 179-187, DOI:10.1007/s00439-012-1238-3 DOI |
7. | Functional polymorphisms in <Emphasis Type="Italic">NFκB1</Emphasis>/<Emphasis Type="Italic">IκBα</Emphasis> predict risks of chronic obstructive pulmonary disease and lung cancer in Chinese Author: Dongsheng Huang, Lei Yang, Yehua Liu, Yumin Zhou, Yuan Guo, Mingan Pan, Yunnan Wang, Yigang Tan, Haibo Zhong, Min Hu, Wenju Lu, Weidong Ji, Jian Wang, Pixin Ran, Nanshan Zhong, Yifeng Zhou, Jiachun Lu Journal: HUMAN GENETICS, 2013, Vol.132, 451-460, DOI:10.1007/s00439-013-1264-9 DOI |
8. | Association between variants of <Emphasis Type="Italic">EXT2</Emphasis> and type 2 diabetes: a replication and meta-analysis Author: Lei Liu, Xu Yang, Haoran Wang, Guanglin Cui, Yujun Xu, Peihua Wang, Gang Yuan, Xiaojing Wang, Hu Ding, Dao Wen Wang Journal: HUMAN GENETICS, 2012, Vol.132, 139-145, DOI:10.1007/s00439-012-1231-x DOI |
9. | Genetic variants at 4q21, 4q23 and 12q24 are associated with esophageal squamous cell carcinoma risk in a Chinese population Author: Yong Gao, Yisha He, Jing Xu, Lin Xu, Jiangbo Du, Chen Zhu, Haiyong Gu, Hongxia Ma, Zhibin Hu, Guangfu Jin, Xiaofei Chen, Hongbing Shen Journal: HUMAN GENETICS, 2013, Vol.132, 649-656, DOI:10.1007/s00439-013-1276-5 DOI |
10. | A miR-570 binding site polymorphism in the <Emphasis Type="Italic">B7</Emphasis>-<Emphasis Type="Italic">H1</Emphasis> gene is associated with the risk of gastric adenocarcinoma Author: Weipeng Wang, Fang Li, Yong Mao, Huan Zhou, Jing Sun, Rui Li, Cuiping Liu, Weichang Chen, Dong Hua, Xueguang Zhang Journal: HUMAN GENETICS, 2013, Vol.132, 641-648, DOI:10.1007/s00439-013-1275-6 DOI |
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