缩写名/全名 |
CLIN GENET
CLINICAL GENETICS |
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ISSN号 | 0009-9163 | ||||||||||||||||||||
研究方向 | 医学-遗传学 | ||||||||||||||||||||
影响因子 | 2015:3.892, 2016:3.326, 2017:3.512, 2018:4.104, 2019:3.578, | ||||||||||||||||||||
出版国家 | DENMARK | ||||||||||||||||||||
出版周期 | Monthly | ||||||||||||||||||||
年文章数 | 141 | ||||||||||||||||||||
出版年份 | 1970 | ||||||||||||||||||||
是否OA | No | ||||||||||||||||||||
审稿周期(仅供参考) | 一般,3-8周 |
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录用比例 | 较易 | ||||||||||||||||||||
投稿链接 | http://mc.manuscriptcentral.com/cge | ||||||||||||||||||||
投稿官网 | http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1399-0004 | ||||||||||||||||||||
h-index | 92 | ||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0009-9163%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. | Genetic risk score modifies the effect of APOE on risk and age onset of Alzheimer's disease. Author: Shi Z1,2,3, Yu H3, Wu Y3,4, Ford M3, Perschon C3, Wang C5, Zheng SL3, Xu J1,2,3,4. Journal: Clin Genet. 2019 Feb;95(2):302-309. doi: 10.1111/cge.13479. Epub 2018 Dec 12. PubMed DOI |
2. | A novel mutation in MYORG causes primary familial brain calcification with central neuropathic pain. Author: Peng Y1, Wang P1, Chen Z1, Jiang H1. Journal: Clin Genet. 2019 Mar;95(3):433-435. doi: 10.1111/cge.13467. Epub 2018 Nov 20. PubMed DOI |
3. | Bi-allelic recessive loss-of-function mutations in FIGLA cause premature ovarian insufficiency with short stature. Author: Yuan P1, He Z2, Sun S3, Li Y1, Wang W1, Liang X2, Xie X3, Jiang Y3, Yang D1. Journal: Clin Genet. 2019 Mar;95(3):409-414. doi: 10.1111/cge.13486. Epub 2018 Dec 18. PubMed DOI |
4. | XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans. Author: Zhang YX1, Li HY1, He WB1,2, Tu C1, Du J1,2, Li W1,2, Lu GX1,2, Lin G1,2, Yang Y3, Tan YQ1,2. Journal: Clin Genet. 2019 Mar;95(3):442-443. doi: 10.1111/cge.13475. Epub 2018 Nov 29. PubMed DOI |
5. | A genome-wide association study identifies new genes associated with developmental dysplasia of the hip. Author: Yan W1, Hao Z2, Tang S3, Dai J1, Zheng L1, Yu P1, Yan W1, Han X1, Xu X1, Shi D1, Ikegawa S4, Teng H5, Jiang Q1,5. Journal: Clin Genet. 2019 Mar;95(3):345-355. doi: 10.1111/cge.13483. Epub 2019 Jan 11. PubMed DOI |
6. | MicroRNA single-nucleotide polymorphisms and diabetes mellitus: A comprehensive review. Author: Zhang Y1, Bai R1, Liu C2, Ma C1, Chen X1, Yang J1, Sun D1. Journal: Clin Genet. 2019 Apr;95(4):451-461. doi: 10.1111/cge.13491. Epub 2019 Jan 15. PubMed DOI |
7. | Novel mutations in WEE2: Expanding the spectrum of mutations responsible for human fertilization failure. Author: Zhang Z1, Mu J1, Zhao J2, Zhou Z1, Chen B1, Wu L3, Yan Z3, Wang W1, Zhao L1, Dong J1, Sun X4, Kuang Y3, Li B3, Wang L5, Sang Q1. Journal: Clin Genet. 2019 Apr;95(4):520-524. doi: 10.1111/cge.13505. Epub 2019 Feb 20. PubMed DOI |
8. | Difficulties and challenges in the development of precision medicine. Author: Liu X1, Luo X2, Jiang C3, Zhao H3. Journal: Clin Genet. 2019 May;95(5):569-574. doi: 10.1111/cge.13511. Epub 2019 Feb 14. PubMed DOI |
9. | Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia. Author: Yan YT1,2, Wei Q1, Zheng Y3, Luo WJ1, Dong HL1, Lu C1, Zhang J1, Chen MJ1, Bao YX1, Li HF1. Journal: Clin Genet. 2019 May;95(5):637-639. doi: 10.1111/cge.13517. Epub 2019 Feb 19. PubMed DOI |
10. | DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella. Author: Li Y1, Sha Y2, Wang X3, Ding L2, Liu W1, Ji Z2, Mei L2, Huang X2, Lin S2, Kong S4, Lu J4, Qin W5, Zhang X5, Zhuang J6, Tang Y5, Lu Z1,4. Journal: Clin Genet. 2019 May;95(5):590-600. doi: 10.1111/cge.13525. Epub 2019 Mar 25. PubMed DOI |
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