缩写名/全名 |
BMC MED GENET
BMC Medical Genetics |
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ISSN号 | 1471-2350 | ||||||||||||||||||||
研究方向 | 医学-遗传学 | ||||||||||||||||||||
影响因子 | 2015:2.094, 2016:2.198, 2017:1.913, 2018:1.74, 2019:1.585, | ||||||||||||||||||||
出版国家 | ENGLAND | ||||||||||||||||||||
出版周期 | Irregular | ||||||||||||||||||||
年文章数 | 201 | ||||||||||||||||||||
出版年份 | 2000 | ||||||||||||||||||||
是否OA | Yes | ||||||||||||||||||||
审稿周期(仅供参考) | 平均12月 |
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录用比例 | 约75% | ||||||||||||||||||||
投稿链接 | http://www.editorialmanager.com/mgtc/default.aspx | ||||||||||||||||||||
投稿官网 | http://bmcmedgenet.biomedcentral.com/ | ||||||||||||||||||||
h-index | 57 | ||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1471-2350%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. | A novel mutation in the OAR domain of <Emphasis Type="Italic">PITX3</Emphasis> associated with congenital posterior subcapsular cataract Author: Qi Fan, Dan Li, Lei Cai, Xiaodi Qiu, Zhennan Zhao, Jihong Wu, Jin Yang, Yi Lu Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0782-2 DOI |
2. | A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family Author: Ningjin Wu, Husile Husile, Liqing Yang, Yaning Cao, Xing Li, Wenyan Huo, Haihua Bai, Yangjian Liu, Qizhu Wu Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0781-3 DOI |
3. | The association between interleukin-6 gene -174G/C single nucleotide polymorphism and sepsis: an updated meta-analysis with trial sequential analysis Author: Yao Chen, Yanyan Hu, Zhenju Song Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0766-2 DOI |
4. | Novel mutations of <Emphasis Type="Italic">STXBP2</Emphasis> and <Emphasis Type="Italic">LYST</Emphasis> associated with adult haemophagocytic lymphohistiocytosis with Epstein-Barr virus infection: a case report Author: Lingshuang Sheng, Wei Zhang, Jia Gu, Kefeng Shen, Hui Luo, Yang Yang Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0765-3 DOI |
5. | Association of vitamin D receptor gene variants with polycystic ovary syndrome: a meta-analysis Author: Xiao-Yuan Shi, Ai-Ping Huang, Duo-Wen Xie, Xiao-Long Yu Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0763-5 DOI |
6. | <Emphasis Type="Italic">TNFSF15</Emphasis> promoter polymorphisms increase the susceptibility to small cell lung cancer: a case-control study Author: Hui Gao, Zeren Niu, Zhi Zhang, Hongjiao Wu, Yuning Xie, Zhenbang Yang, Ang Li, Zhenxian Jia, Xuemei Zhang Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0762-6 DOI |
7. | A functional variant alters binding of activating protein 1 regulating expression of <Emphasis Type="Italic">FGF7</Emphasis> gene associated with chronic obstructive pulmonary disease Author: Xiaomei Zhang, Yongxin Guo, Jing Yang, Jianlou Niu, Lina Du, Haiyan Li, Xiaokun Li Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0761-7 DOI |
8. | <Emphasis Type="Italic">ATM</Emphasis> rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis Author: Zhi-liang Zhao, Lu Xia, Cong Zhao, Jun Yao Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0760-8 DOI |
9. | Whole-exome sequencing identifies a novel missense variant within <Emphasis Type="Italic">LOXHD1</Emphasis> causing rare hearing loss in a Chinese family Author: Na Shen, Ting Wang, Delei Li, Aiguo Liu, Yanjun Lu Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0758-2 DOI |
10. | Association between polymorphisms in the <Emphasis Type="Italic">GRIN1</Emphasis> gene 5′ regulatory region and schizophrenia in a northern Han Chinese population and haplotype effects on protein expression in vitro Author: Yong-ping Liu, Mei Ding, Xi-cen Zhang, Yi Liu, Jin-feng Xuan, Jia-xin Xing, Xi Xia, Jun Yao, Bao-jie Wang Journal: BMC Medical Genetics, 2019, Vol.20, , DOI:10.1186/s12881-019-0757-3 DOI |
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