| 缩写名/全名 |
AM J MED GENET C
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS |
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| ISSN号 | 1552-4868 | ||||||||||||||||||||
| 研究方向 | 医学-遗传学 | ||||||||||||||||||||
| 影响因子 | 2015:4.471, 2016:5.6, 2017:3.822, 2018:5.683, 2019:7.101, | ||||||||||||||||||||
| 出版国家 | UNITED STATES | ||||||||||||||||||||
| 出版周期 | Quarterly | ||||||||||||||||||||
| 年文章数 | 49 | ||||||||||||||||||||
| 出版年份 | 2003 | ||||||||||||||||||||
| 是否OA | No | ||||||||||||||||||||
| 审稿周期(仅供参考) | >12周，或约稿 |
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| 录用比例 | 一般 | ||||||||||||||||||||
| 投稿链接 | https://mc.manuscriptcentral.com/ajmg-c | ||||||||||||||||||||
| 投稿官网 | http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-4876 | ||||||||||||||||||||
| h-index | 93 | ||||||||||||||||||||
| CiteScore |
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| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1552-4868%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. | The rise of the genetic counseling profession in China. Author: Sun L1,2, Liang B3, Zhu L2, Shen Y4,5,6,7, He L1,3,2,8. Journal: Am J Med Genet C Semin Med Genet. 2019 Mar 12. doi: 10.1002/ajmg.c.31693. [Epub ahead of print] PubMed DOI |
| 2. | Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorder. Author: Chen F1, Yuan H2, Wu W3, Chen S1, Yang Q1, Wang J1, Zhang Q1, Gui B1, Fan X1, Chen R3, Shen Y1,4,5,6. Journal: Am J Med Genet C Semin Med Genet. 2019 Mar 20. doi: 10.1002/ajmg.c.31698. [Epub ahead of print] PubMed DOI |
| 3. | Genetic studies on systemic lupus erythematosus in East Asia point to population differences in disease susceptibility. Author: Wang YF1, Lau YL1, Yang W1. Journal: Am J Med Genet C Semin Med Genet. 2019 Mar 21. doi: 10.1002/ajmg.c.31696. [Epub ahead of print] PubMed DOI |
| 4. | The different facets of "culture" in genetic counseling: A situated analysis of genetic counseling in Hong Kong. Author: Zayts O1, Shipman H1, Fung JL2, Liu AP2, Kwok SY3, Tsai AC4, Yung TC3, Chung BH2. Journal: Am J Med Genet C Semin Med Genet. 2019 May 2. doi: 10.1002/ajmg.c.31699. [Epub ahead of print] PubMed DOI |
| 5. | Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia. Author: Wasant P1,2, Padilla C3, Lam S4, Thong MK5, Lai PS6. Journal: Am J Med Genet C Semin Med Genet. 2019 May 3. doi: 10.1002/ajmg.c.31701. [Epub ahead of print] PubMed DOI |
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