| 缩写名/全名 |
HUM MOL GENET
HUMAN MOLECULAR GENETICS |
||||||||||||||||||||||||
| ISSN号 | 0964-6906 | ||||||||||||||||||||||||
| 研究方向 | 生物-生化与分子生物学 | ||||||||||||||||||||||||
| 影响因子 | 2015:5.985, 2016:5.34, 2017:4.902, 2018:4.544, 2019:5.1, | ||||||||||||||||||||||||
| 出版国家 | ENGLAND | ||||||||||||||||||||||||
| 出版周期 | Semimonthly | ||||||||||||||||||||||||
| 年文章数 | 345 | ||||||||||||||||||||||||
| 出版年份 | 1992 | ||||||||||||||||||||||||
| 是否OA | No | ||||||||||||||||||||||||
| 审稿周期(仅供参考) | 较快,2-4周 |
||||||||||||||||||||||||
| 录用比例 | 较难 | ||||||||||||||||||||||||
| 投稿链接 | http://www.oxfordjournals.org/our_journals/hmg/for_authors/submission_online.html | ||||||||||||||||||||||||
| 投稿官网 | http://hmg.oxfordjournals.org/ | ||||||||||||||||||||||||
| h-index | 255 | ||||||||||||||||||||||||
| CiteScore |
|
||||||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0964-6906%5BISSN%5D | ||||||||||||||||||||||||
| 中科院SCI期刊分区 （ 2018年新版本） |
|
||||||||||||||||||||||||
| 中科院SCI期刊分区 （ 2020年新版本） |
|
| 中国学者近期发表的论文 | |
| 1. | Loss of MeCP2 in immature neurons leads to impaired network integration. Author: Sun Y1,2,3, Gao Y3,4, Tidei JJ3,4, Shen M3,4, Hoang JT3,4, Wagner DF3,4, Zhao X3,4,5. Journal: Hum Mol Genet. 2019 Jan 15;28(2):245-257. doi: 10.1093/hmg/ddy338. PubMed DOI |
| 2. | Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy. Author: Sommerville EW1, Zhou XL2, Oláhová M1, Jenkins J3, Euro L4, Konovalova S4, Hilander T4, Pyle A1, He L1, Habeebu S3, Saunders C3,5,6, Kelsey A7, Morris AAM7, McFarland R1, Suomalainen A4,8,9, Gorman GS1, Wang ED2, Thiffault I3,5,6, Tyynismaa H4, Taylor RW1. Journal: Hum Mol Genet. 2019 Jan 15;28(2):258-268. doi: 10.1093/hmg/ddy294. PubMed DOI |
| 3. | TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice. Author: Yang N1,2,3, Wu N4,5,6,7, Zhang L1, Zhao Y4,5, Liu J4,5, Liang X8, Ren X1, Li W1, Chen W4,5, Dong S1, Zhao S4,5, Lin J4,5, Xiang H1, Xue H9, Chen L1, Sun H9, Zhang J4,5,6, Shi J10, Zhang S5,11, Lu D1, Wu X12, Jin L1, Ding J8, Qiu G4,5,6, Wu Z4,5,13, Lupski JR7,14,15, Zhang F1,2,3. Journal: Hum Mol Genet. 2019 Feb 15;28(4):539-547. doi: 10.1093/hmg/ddy358. PubMed DOI |
| 4. | CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms. Author: Tu Z1, Zhao H2,3, Li B1, Yan S1, Wang L4, Tang Y4, Li Z1, Bai D1, Li C1, Lin Y1, Li Y5, Liu J6, Xu H4, Guo X1, Jiang YH7, Zhang YQ2, Li XJ1,8. Journal: Hum Mol Genet. 2019 Feb 15;28(4):561-571. doi: 10.1093/hmg/ddy367. PubMed DOI |
| 5. | Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection. Author: Takeuchi F1, Kukimoto I2, Li Z3,4,5,6, Li S7, Li N8, Hu Z9,10, Takahashi A11,12, Inoue S13, Yokoi S14,15, Chen J4,5,16, Hang D9, Kuroda M17, Matsuda F18, Mizuno M19, Mori S2, Wu P7, Tanaka N20, Matsuo K13,21, Kamatani Y11,18, Kubo M22, Ma D7, Shi Y3,4,5,6,16. Journal: Hum Mol Genet. 2019 Jan 15;28(2):341-348. doi: 10.1093/hmg/ddy390. PubMed DOI |
| 6. | A fusion peptide directs enhanced systemic dystrophin exon skipping and functional restoration in dystrophin-deficient mdx mice. Author: Yin H1,2, Moulton HM3, Betts C1, Seow Y1, Boutilier J3, Iverson PL3, Wood MJA1. Journal: Hum Mol Genet. 2019 Feb 15;28(4):699. doi: 10.1093/hmg/ddy377. PubMed DOI |
| 7. | Causal effects of blood lipids on amyotrophic lateral sclerosis: a Mendelian randomization study. Author: Zeng P1, Zhou X2. Journal: Hum Mol Genet. 2019 Feb 15;28(4):688-697. doi: 10.1093/hmg/ddy384. PubMed DOI |
| 8. | Impact of Fgf10 deficiency on pulmonary vasculature formation in a mouse model of bronchopulmonary dysplasia. Author: Chao CM1,2,3, Moiseenko A2, Kosanovic D2, Rivetti S2, El Agha E1,2, Wilhelm J2, Kampschulte M4, Yahya F2, Ehrhardt H3, Zimmer KP3, Barreto G5,6, Rizvanov AA6, Schermuly RT2, Reiss I7, Morty RE5, Rottier RJ8,9, Bellusci S1,2,6, Zhang JS1. Journal: Hum Mol Genet. 2019 May 1;28(9):1429-1444. doi: 10.1093/hmg/ddy439. PubMed DOI |
| 9. | Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy. Author: Ji Y1,2, Zhang J2,3,4, Yu J1,2, Wang Y5, Lu Y3,4, Liang M4, Li Q1,2, Jin X1, Wei Y2, Meng F1,2, Gao Y2, Cang X1,2, Tong Y3,4, Liu X3,4, Zhang M6, Jiang P1, Zhu T7, Mo JQ8, Huang T9, Jiang P1,2, Guan MX1,2,10,11. Journal: Hum Mol Genet. 2019 May 1;28(9):1515-1529. doi: 10.1093/hmg/ddy450. PubMed DOI |
| 10. | CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection. Author: Ouyang J1, Sun W1, Xiao X1, Li S1, Jia X1, Zhou L1, Wang P1, Zhang Q1. Journal: Hum Mol Genet. 2019 Jan 26. doi: 10.1093/hmg/ddz029. [Epub ahead of print] PubMed DOI |
|
|
