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以下是对 CLIN GENET 杂志介绍 收藏
缩写名/全名
CLIN GENET
CLINICAL GENETICS
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
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
CiteScoreSJRSNIPCiteScore排名
3.141.6791.220
学科分区排名
大类:Medicine
小类:Genetics(clinical)
Q232 / 91
大类:Biochemistry, Genetics and Molecular Biology
小类:Genetics
Q2103 / 318

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)
大类学科小类学科Top期刊综述期刊
医学 2区2区1区
GENETICS & HEREDITY
遗传学
1区2区3区
中科院SCI期刊分区
( 2020年新版本)
大类学科小类学科Top期刊综述期刊
医学 1区2区1区
GENETICS & HEREDITY
遗传学
2区4区2区
  • 该杂志上中国学者近期发表的论文
  • 同领域相关期刊
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
同类著名期刊名称 h-index CiteScore
NATURE REVIEWS GENETICS32016.63
NATURE GENETICS52719.88
TRENDS IN GENETICS2088.34
Annual Review of Genetics17110.11
AMERICAN JOURNAL OF HUMAN GENETICS2808.64
GENETICS IN MEDICINE1118.26
Annual Review of Genomics and Human Genetics1049.15
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS934.71
HUMAN GENETICS1264.34
PLoS Genetics1945.00
中科院JCR同大类学科的热搜期刊 浏览次数
MEDICINE287604
CANCER RESEARCH163772
International Journal of Nanomedicine162227
Molecular Medicine Reports162125
CANCER LETTERS157297
JOURNAL OF ETHNOPHARMACOLOGY139136
BIOMEDICINE & PHARMACOTHERAPY137165
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY133789
Theranostics133108
International Journal of Environmental Research and Public Health131430