缩写名/全名 |
EUR J HUM GENET
EUROPEAN JOURNAL OF HUMAN GENETICS |
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ISSN号 | 1018-4813 | ||||||||||||||||||||
研究方向 | 生物-生化与分子生物学 | ||||||||||||||||||||
影响因子 | 2015:4.58, 2016:4.287, 2017:3.636, 2018:3.65, 2019:3.657, | ||||||||||||||||||||
出版国家 | ENGLAND | ||||||||||||||||||||
出版周期 | Monthly | ||||||||||||||||||||
年文章数 | 193 | ||||||||||||||||||||
出版年份 | 1992 | ||||||||||||||||||||
是否OA | No | ||||||||||||||||||||
审稿周期(仅供参考) | 平均2月 |
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录用比例 | 约50% | ||||||||||||||||||||
投稿链接 | http://mts-ejhg.nature.com/cgi-bin/main.plex | ||||||||||||||||||||
投稿官网 | http://www.nature.com/ejhg/index.html | ||||||||||||||||||||
h-index | 116 | ||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1018-4813%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. | Linear isoforms of the long noncoding RNA CDKN2B-AS1 regulate the c-myc-enhancer binding factor RBMS1. Author: Hubberten M1, Bochenek G2, Chen H1,3, Häsler R4, Wiehe R1, Rosenstiel P4, Jepsen S2, Dommisch H1, Schaefer AS5. Journal: Eur J Hum Genet. 2019 Jan;27(1):80-89. doi: 10.1038/s41431-018-0210-7. Epub 2018 Aug 14. PubMed DOI |
2. | MultiWaver 2.0: modeling discrete and continuous gene flow to reconstruct complex population admixtures. Author: Ni X1, Yuan K2,3, Liu C2,3, Feng Q2,3, Tian L2,3, Ma Z4,5,6, Xu S7,8,9,10,11. Journal: Eur J Hum Genet. 2019 Jan;27(1):133-139. doi: 10.1038/s41431-018-0259-3. Epub 2018 Sep 11. PubMed DOI |
3. | Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples. Author: Zhao S1,2, Xiang J3, Fan C1,2, Asan1,2, Shang X4, Zhang X5, Chen Y6, Zhu B7, Cai W8, Chen S9, Cai R10, Guo X11, Zhang C12, Zhou Y13, Huang S14, Liu Y15, Chen B16, Yan S17, Chen Y18, Ding H19, Guo F1,2, Wang Y1,2, Zhong W1,2, Zhu Y1,2, Wang Y1,2, Chen C1,2, Li Y20, Huang H3, Mao M3, Yin Y3, Wang J21,22, Yang H21,22, Xu X4, Sun J23,24, Peng Z25,26. Journal: Eur J Hum Genet. 2019 Feb;27(2):254-262. doi: 10.1038/s41431-018-0253-9. Epub 2018 Oct 1. PubMed DOI |
4. | The Global State of the Genetic Counseling Profession. Author: Abacan M1, Alsubaie L2, Barlow-Stewart K3, Caanen B4, Cordier C5, Courtney E6, Davoine E7, Edwards J8, Elackatt NJ9, Gardiner K10, Guan Y11, Huang LH12,13, Malmgren CI14,15,16,17, Kejriwal S18, Kim HJ19, Lambert D20, Lantigua-Cruz PA21, Lee JMH22, Lodahl M23, Lunde Å24, Macaulay S25, Macciocca I26, Margarit S27, Middleton A28,29, Moldovan R30, Ngeow J6, Obregon-Tito AJ31, Ormond KE32,33, Paneque M34, Powell K35, Sanghavi K36, Scotcher D37, Scott J38, Juhé CS39, Shkedi-Rafid S40, Wessels TM41, Yoon SY42,43,22, Wicklund C44. Journal: Eur J Hum Genet. 2019 Feb;27(2):183-197. doi: 10.1038/s41431-018-0252-x. Epub 2018 Oct 5. PubMed DOI |
5. | The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility. Author: Chen B1, Wang W1, Peng X2, Jiang H2,3, Zhang S4, Li D5, Li B4, Fu J2, Kuang Y4, Sun X2, Wang X1, Zhang Z1, Wu L4, Zhou Z1, Lyu Q4, Yan Z4, Mao X4, Xu Y1, Mu J1, Li Q1, Jin L1, He L6, Sang Q7, Wang L8,9. Journal: Eur J Hum Genet. 2019 Feb;27(2):300-307. doi: 10.1038/s41431-018-0283-3. Epub 2018 Oct 8. PubMed DOI |
6. | Autonomous decision-making for antenatal screening in Pakistan: views held by women, men and health professionals in a low-middle income country. Author: Ahmed S1, Jafri H2, Rashid Y3, Yi H4, Dong D5, Zhu J6, Ahmed M7. Journal: Eur J Hum Genet. 2019 Jun;27(6):848-856. doi: 10.1038/s41431-019-0353-1. Epub 2019 Feb 4. PubMed DOI |
7. | SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections. Author: Duan XY1, Guo DC1, Regalado ES1, Shen H1,2; University of Washington Center for Mendelian Genomics, Coselli JS3,4, Estrera AL4, Safi HJ5, Bamshad MJ6, Nickerson DA6, LeMaire SA3,4, De Backer J7, Milewicz DM8. Journal: Eur J Hum Genet. 2019 Feb 26. doi: 10.1038/s41431-019-0357-x. [Epub ahead of print] PubMed DOI |
8. | Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array. Author: Rodriguez S, Gaunt TR, Guo Y, Zheng J, Barnes MR, Tang W, Danish F, Johnson A, Castillo BA, Li YR, Hakonarson H, Buxbaum SG, Palmer T, Tsai MY, Lange LA, Ebrahim S, Davey Smith G, Lawlor DA, Folsom AR, Hoogeveen R, Reiner A, Keating B, Day IN. Journal: Eur J Hum Genet. 2016 Jan;24(1):106-12. doi: 10.1038/ejhg.2015.63. Epub 2015 Apr 29. PubMed |
9. | Refined phylogenetic structure of an abundant East Asian Y-chromosomal haplogroup O*-M134. Author: Ning C, Yan S, Hu K, Cui YQ, Jin L. Journal: Eur J Hum Genet. 2016 Feb;24(2):307-9. doi: 10.1038/ejhg.2015.183. Epub 2015 Aug 26. PubMed |
10. | A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy. Author: Qu YJ, Bai JL, Cao YY, Zhang WH, Wang H, Jin YW, Song F. Journal: Eur J Hum Genet. 2016 Jun;24(6):864-70. doi: 10.1038/ejhg.2015.213. Epub 2015 Sep 30. PubMed |
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