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HUMAN MUTATION

2023年12月最新中科院分区表数据已经更新,欢迎查询! 如果您对期刊系统有任何需求或者问题,欢迎点击此处反馈给我们。

按期刊名首写字母查看 HUM MUTAT最新评论:请问你们有ae invited阶段吗,我都一个多月了还是unassigned (2023-08-28)


期刊名:   ISSN:   研究方向:   影响因子: -   SCI收录:
大类学科:   小类学科:   中科院分区:   是否OA期刊:   结果排序:

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HUMAN MUTATION期刊基本信息Hello,您是该期刊的第38037位访客


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期刊名字HUMAN MUTATIONHUMAN MUTATION

HUM MUTAT
(此期刊被最新的JCR期刊SCIE收录)

LetPub评分
7.7
53人评分
我要评分

声誉
8.7

影响力
6.6

速度
9.4

期刊ISSN1059-7794
微信扫码收藏此期刊
E-ISSN1098-1004
2022-2023最新影响因子
(数据来源于搜索引擎)
3.9 点击查看影响因子趋势图
实时影响因子 截止2024年3月26日:3.324
2022-2023自引率5.10%点击查看自引率趋势图
五年影响因子4.5
h-index 146
CiteScore
CiteScoreSJRSNIPCiteScore排名
7.901.5381.507
学科分区排名百分位
大类:Medicine
小类:Genetics (clinical)
Q120 / 90
大类:Medicine
小类:Genetics
Q172 / 328

期刊简介
Human Mutation is a peer-reviewed journal that offers publication of original Research Articles, Methods, Mutation Updates, Reviews, Database Articles, Rapid Communications, and Letters on broad aspects of mutation research in humans. Reports of novel DNA variations and their phenotypic consequences, reports of SNPs demonstrated as valuable for genomic analysis, descriptions of new molecular detection methods, and novel approaches to clinical diagnosis are welcomed. Novel reports of gene organization at the genomic level, reported in the context of mutation investigation, may be considered. The journal provides a unique forum for the exchange of ideas, methods, and applications of interest to molecular, human, and medical geneticists in academic, industrial, and clinical research settings worldwide.
期刊官方网站http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004
期刊投稿网址http://mc.manuscriptcentral.com/humu
期刊语言要求Language
Manuscripts must be written in American English and be grammatically and linguistically correct. Authors should seek assistance with style, grammar and vocabulary if necessary. Your manuscript may also be sent back to you for revision if the quality of English language is poor.

经LetPub语言功底雄厚的美籍native English speaker精心编辑的稿件,不仅能满足HUMAN MUTATION的语言要求,还能让HUMAN MUTATION编辑和审稿人得到更好的审稿体验,让稿件最大限度地被HUMAN MUTATION编辑和审稿人充分理解和公正评估。LetPub的专业SCI论文编辑服务(包括SCI论文英语润色同行资深专家修改润色SCI论文专业翻译SCI论文格式排版专业学术制图等)帮助作者准备稿件,已助力全球15万+作者顺利发表论文。部分发表范例可查看:服务好评 论文致谢
提交文稿
是否OA开放访问No
通讯方式WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030
出版商Wiley-Liss Inc.
涉及的研究方向医学-遗传学
出版国家或地区UNITED STATES
出版语言English
出版周期Monthly
出版年份1992
年文章数 150点击查看年文章数趋势图
Gold OA文章占比76.92%
研究类文章占比:
文章 ÷(文章 + 综述)
90.00%
WOS期刊SCI分区
2022-2023年最新版
WOS分区等级:2区

按学科分区JIF分区JIF排名JIF百分位
学科:GENETICS & HEREDITY
类别:SCIE
Q251/171
中科院《国际期刊预警
名单(试行)》名单
2024年02月发布的2024版:不在预警名单中

2023年01月发布的2023版:不在预警名单中

2021年12月发布的2021版:不在预警名单中

2020年12月发布的2020版:不在预警名单中
中科院SCI期刊分区
2023年12月最新升级版
点击查看中科院SCI期刊分区趋势图
大类学科小类学科Top期刊综述期刊
医学 1区2区4区
GENETICS & HEREDITY
遗传学
4区3区2区
中科院SCI期刊分区
2022年12月升级版
大类学科小类学科Top期刊综述期刊
医学 3区2区1区
GENETICS & HEREDITY
遗传学
1区4区2区
中科院SCI期刊分区
2021年12月旧的升级版
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
3区3区2区
SCI期刊收录coverage Science Citation Index Expanded (SCIE) (2020年1月,原SCI撤销合并入SCIE,统称SCIE)
Scopus (CiteScore)
PubMed Central (PMC)链接http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1059-7794%5BISSN%5D
平均审稿速度网友分享经验:
平均3.0个月
平均录用比例网友分享经验:
约50%
LetPub助力发表经LetPub编辑的稿件平均录用比例是未经润色的稿件的1.5倍,平均审稿时间缩短40%。众多作者在使用LetPub的专业SCI论文编辑服务(包括SCI论文英语润色同行资深专家修改润色SCI论文专业翻译SCI论文格式排版专业学术制图等)后论文在HUMAN MUTATION顺利发表。
快看看作者怎么说吧:服务好评 论文致谢
期刊常用信息链接
同领域相关期刊 HUMAN MUTATION期刊近年CiteScore指标趋势图
该杂志的自引率趋势图 HUMAN MUTATION中科院SCI期刊分区趋势图
该杂志的年文章数趋势图 同领域作者分享投稿经验
HUMAN MUTATION上中国学者近期发表的论文  
  • 同领域相关期刊
  • 期刊CiteScore趋势图
  • 期刊自引率趋势图
  • 中科院SCI期刊分区趋势图
  • 年文章数趋势图
  • 该期刊中国学者近期发表论文
  • 中科院SCI期刊分区相关期刊
  • 同类著名期刊名称 h-index CiteScore
    NATURE REVIEWS GENETICS32073.20
    NATURE GENETICS52753.80
    TRENDS IN GENETICS20818.10
    Annual Review of Genetics17119.80
    AMERICAN JOURNAL OF HUMAN GENETICS28017.20
    GENETICS IN MEDICINE11115.40
    Annual Review of Genomics and Human Genetics10415.10
    HUMAN GENETICS1269.70
    PLoS Genetics1949.00
    DNA RESEARCH897.10
    中科院SCI期刊分区同大类学科的热搜期刊 浏览次数
    MEDICINE616648
    BIOMATERIALS524481
    BIOMEDICINE & PHARMACOTHERAPY481235
    Journal of Materials Chemistry B468347
    Frontiers in Pharmacology463648
    Frontiers in Immunology436668
    JOURNAL OF ETHNOPHARMACOLOGY417596
    COLLOIDS AND SURFACES B-BIOINTERFACES411155
    Frontiers in Oncology395163
    COMPUTERS IN BIOLOGY AND MEDICINE387553
  •  

    HUMAN MUTATION HUMAN MUTATION
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  • 中国学者近期发表的论文
    1.Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation.

    Author: Han M1, Zhao M1, Cheng C1, Huang Y2, Han S3, Li W1, Tu X1, Luo X1, Yu X1, Liu Y1, Chen Q4,5, Ren X1, Wang QK1,4,5, Ke T1.
    Journal: Hum Mutat. 2019 Mar;40(3):310-325. doi: 10.1002/humu.23691. Epub 2018 Dec 8.
        PubMed      DOI
    2.A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathy.

    Author: Chen X1,2, Jin J1,3, Wang Q1,4, Xue H1,3, Zhang N1, Du Y1,5, Zhang T1, Zhang B1, Wu J1, Liu Z1.
    Journal: Hum Mutat. 2019 Mar;40(3):281-287. doi: 10.1002/humu.23690. Epub 2018 Dec 8.
        PubMed      DOI
    3.A novel mutation of PANK4 causes autosomal dominant congenital posterior cataract.

    Author: Sun M1, Chen C1, Hou S2, Li X1, Wang H3, Zhou J1, Chen X1, Liu P1, Kijlstra A4, Lin S1, Ye J1.
    Journal: Hum Mutat. 2019 Apr;40(4):380-391. doi: 10.1002/humu.23696. Epub 2019 Jan 23.
        PubMed      DOI
    4.Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification.

    Author: Guo XX1, Zou XH1, Wang C1, Yao XP1, Su HZ1, Lai LL1, Chen HT2, Lai JH3, Liu YB4, Chen DP5, Deng YC6, Lin P7, Lin HS8, Hong BC9, Yao QY9, Chen XJ10, Huang DQ11, Fu HX12, Peng JD13, Niu YF14, Zhao YY15, Zhu XQ16, Lu XP17, Lin HL18, Li YK19, Liu CY20, Huang GB21, Wang N1,22, Chen WJ1,22.
    Journal: Hum Mutat. 2019 Apr;40(4):392-403. doi: 10.1002/humu.23703. Epub 2019 Jan 15.
        PubMed      DOI
    5.UVEOGENE: An SNP database for investigations on genetic factors associated with uveitis and their relationship with other systemic autoimmune diseases.

    Author: Wang Q1, Su G1, Tan X1, Deng J1, Du L1, Huang X1, Lv M1, Yi S1, Hou S1, Kijlstra A2, Yang P1.
    Journal: Hum Mutat. 2019 Mar;40(3):258-266. doi: 10.1002/humu.23702. Epub 2019 Jan 16.
        PubMed      DOI
    6.Complex ATP7B mutation patterns in Wilson disease and evaluation of a yeast model for functional analysis of variants.

    Author: Li X1,2,3, Zhang W4,2,3, Zhou D1,2,3, Lv T1,2,3, Xu A1,2,3, Wang H1,2,3, Zhao X4,2,3, Zhang B1,2,3, Li Y1,2,3, Jia S1,2,3, Wang Y4,2,3, Wang X4,2,3, Wu Z4,2,3, Duan W4,2,3, Wang Q4,2,3, Nan Y5, Shang J6, Jiang W7, Chen Y8, Zheng S9, Liu M9, Sun L10, You H1,4,2,3, Jia J4,2,3, Ou X4,2,3, Huang J1,4,2,3.
    Journal: Hum Mutat. 2019 May;40(5):552-565. doi: 10.1002/humu.23714. Epub 2019 Feb 14.
        PubMed      DOI
    7.Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta.

    Author: Li L1, Mao B1, Li S1, Xiao J1, Wang H1, Zhang J1, Ren X2, Wang Y3, Wu Y1, Cao Y1, Lu C1, Gao J4, You Y1, Zhao F1, Geng X1, Xiao Y1, Jiang C1, Ye Y1, Yang T1, Zhao X1, Zhang X1.
    Journal: Hum Mutat. 2019 May;40(5):588-600. doi: 10.1002/humu.23718. Epub 2019 Feb 25.
        PubMed      DOI
    8.Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.

    Author: Zhou WZ1,2, Zhang J1, Li Z1, Lin X3, Li J1, Wang S3,4, Yang C3,5, Wu Q6, Ye AY1,7,8, Wang M1, Wang D3, Pu TZ9, Wu YY10, Wei L1.
    Journal: Hum Mutat. 2019 Jun;40(6):801-815. doi: 10.1002/humu.23724. Epub 2019 Apr 29.
        PubMed      DOI
    9.SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals.

    Author: Ng BG1, Sosicka P1, Agadi S2, Almannai M2, Bacino CA2,3, Barone R4,5, Botto LD6, Burton JE7, Carlston C8, Chung BH9, Cohen JS10, Coman D11,12, Dipple KM13,14,15, Dorrani N16, Dobyns WB17,18, Elias AF19, Epstein L20, Gahl WA21,22, Garozzo D5, Hammer TB23, Haven J19, Héron D24, Herzog M15, Hoganson GE7, Hunter JM25, Jain M10, Juusola J26, Lakhani S27, Lee H15,28, Lee J29,30, Lewis K11, Longo N6, Lourenço CM31, Mak CCY9, McKnight D26, Mendelsohn BA32, Mignot C24, Mirzaa G17,18, Mitchell W33,34, Muhle H35, Nelson SF15,28,36, Olczak M37, Palmer CGS15,36,38, Partikian A39, Patterson MC40, Pierson TM41,42,43, Quinonez SC44, Regan BM45, Ross ME27, Guillen Sacoto MJ26, Scaglia F2,3,46, Scheffer IE45,47, Segal D27,48, Singhal NS49, Striano P50, Sturiale L5, Symonds JD51, Tang S25, Vilain E52, Willis M53, Wolfe LA21,22, Yang H26, Yano S54, Powis Z25, Suchy SF25, Rosenfeld JA26, Edmondson AC2, Grunewald S55, Freeze HH56.
    Journal: Hum Mutat. 2019 Feb 28. doi: 10.1002/humu.23731. [Epub ahead of print]
        PubMed      DOI
    10.Identification of a p.Trp403* nonsense variant in PHEX causing X-linked hypophosphatemia by inhibiting p38 MAPK signaling.

    Author: Li W1, Tan L2, Li X2, Zhang X1, Wu X2, Chen H2, Hu L3, Wang X3, Luo X4, Wang F5,6,7, Xu C1, Chen Q5,6,7, Jin R2, Wang QK1,5,6,7.
    Journal: Hum Mutat. 2019 Mar 28. doi: 10.1002/humu.23743. [Epub ahead of print]
        PubMed      DOI
  • 同大类学科的其他著名期刊名称 h-index CiteScore
    CA-A CANCER JOURNAL FOR CLINICIANS144642.90
    LANCET700133.20
    NEW ENGLAND JOURNAL OF MEDICINE933134.40
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION62245.40
    NATURE REVIEWS DRUG DISCOVERY289123.80
    BMJ-British Medical Journal015.30
    BMJ-British Medical Journal015.30
    NATURE REVIEWS IMMUNOLOGY35183.00
    NATURE MEDICINE497107.50
    Nature Reviews Disease Primers4860.90
    同分区等级的其他期刊名称 h-index CiteScore
    Living Reviews in Relativity065.50
    Living Reviews in Relativity7565.50
    JOURNAL OF TRAVEL MEDICINE5119.60
    Military Medical Research030.10
    Advanced Composites and Hybrid Materials016.90
    INTERNATIONAL JOURNAL OF COMPUTER VISION17222.50
    Eurosurveillance9027.70
    JOURNAL OF THE ROYAL SOCIETY OF MEDICINE715.70
    Small Structures00.00
    Trends in Chemistry032.10


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