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HUMAN GENETICS

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 GENET最新评论:审稿速度:1.0 | 投稿命中率:75.0偏重的研究方向:基因功能;临床经验分享:杂志反应很快,同级别的杂志中,可以优先投这个。投过... (2022-12-15)


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 GENETICS期刊基本信息Hello,您是该期刊的第56914位访客

基本信息 登录收藏
期刊名字HUMAN GENETICSHUMAN GENETICS

HUM GENET
(此期刊被最新的JCR期刊SCIE收录)

LetPub评分
7.7
50人评分
我要评分

声誉
8.8

影响力
6.6

速度
9.2

期刊ISSN0340-6717
微信扫码收藏此期刊
E-ISSN1432-1203
2022-2023最新影响因子
(数据来源于搜索引擎)
5.3 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:4.134
2022-2023自引率3.80%点击查看自引率趋势图
五年影响因子5.2
h-index 126
CiteScore
CiteScoreSJRSNIPCiteScore排名
9.701.9801.653
学科分区排名百分位
大类:Medicine
小类:Genetics (clinical)
Q18 / 90
大类:Medicine
小类:Genetics
Q143 / 328

期刊简介
Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology.
Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted.

The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
期刊官方网站https://www.springer.com/439
期刊投稿网址https://www.editorialmanager.com/huge
作者指南网址https://www.springer.com/439/submission-guidelines
期刊语言要求Language
Presenting your work in a well-structured manuscript and in well-written English gives it its best chance for editors and reviewers to understand it and evaluate it fairly. Many researchers find that getting some independent support helps them present their results in the best possible light.

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 GENETICS的语言要求,还能让HUMAN GENETICS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 GENETICS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SPRINGER, 233 SPRING ST, NEW YORK, USA, NY, 10013
出版商Springer Berlin Heidelberg
涉及的研究方向生物-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1964
年文章数 94点击查看年文章数趋势图
Gold OA文章占比30.30%
研究类文章占比:
文章 ÷(文章 + 综述)
85.11%
WOS期刊SCI分区
2022-2023年最新版
WOS分区等级:1区

按学科分区JIF分区JIF排名JIF百分位
学科:GENETICS & HEREDITY
类别:SCIE
Q127/171
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
生物学 4区2区4区
GENETICS & HEREDITY
遗传学
4区4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
生物学 3区2区2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
生物学 1区2区2区
GENETICS & HEREDITY
遗传学
1区1区3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=0340-6717%5BISSN%5D
平均审稿速度网友分享经验:
平均1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 GENETICS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 GENETICS期刊近年CiteScore指标趋势图
该杂志的自引率趋势图 HUMAN GENETICS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 GENETICS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
    PLoS Genetics1949.00
    DNA RESEARCH897.10
    JOURNAL OF MEDICAL GENETICS1599.60
    中科院SCI期刊分区同大类学科的热搜期刊 浏览次数
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES1184637
    Frontiers in Plant Science719378
    Frontiers in Microbiology704435
    BIOSENSORS & BIOELECTRONICS589618
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS543433
    PeerJ414645
    BMC GENOMICS409845
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY397268
    JOURNAL OF BIOLOGICAL CHEMISTRY383885
    Cell Death & Disease371458
  •  

    HUMAN GENETICS HUMAN GENETICS
    我来预测明年:
    稳步上升 表现平稳 逐渐下降  刷新
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  • 中国学者近期发表的论文
    1.Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss

    Author: Xiang, Jiale; Sun, Xiangzhong; Song, Nana; Ramaswamy, Sathishkumar; Abou Tayoun, Ahmad N.; Peng, Zhiyu
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 33-43. DOI: 10.1007/s00439-022-02479-0
        PubMed      DOI
    2.Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformation

    Author: Liu, Zhenlei; Du, Huakang; Zhao, Hengqiang; Cai, Siyi; Zhao, Sen; Niu, Yuchen; Li, Xiaoxin; Liu, Bowen; Huang, Yingzhao; Shao, Jiashen; Liu, Lian; Tian, Ye; Wu, Zhihong; Wu, Hao; Hu, Yue; Zhang, Terry Jianguo; Jian, Fengzeng; Wu, Nan
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 89-101. DOI: 10.1007/s00439-022-02474-5
        PubMed      DOI
    3.Truncation mutations in MYRF underlie primary angle closure glaucoma

    Author: Ouyang, Jiamin; Sun, Wenmin; Shen, Huangxuan; Liu, Xing; Wu, Yingchen; Jiang, Hongmei; Li, Xueqing; Wang, Yingwei; Jiang, Yi; Li, Shiqiang; Xiao, Xueshan; Hejtmancik, J. Fielding; Tan, Zhiqun; Zhang, Qingjiong
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 1, pp. 103-123. DOI: 10.1007/s00439-022-02487-0
        PubMed      DOI
    4.Common genetic risk factors in ASD and ADHD co-occurring families

    Author: Zhou, Anbo; Cao, Xiaolong; Mahaganapathy, Vaidhyanathan; Azaro, Marco; Gwin, Christine; Wilson, Sherri; Buyske, Steven; Bartlett, Christopher W.; Flax, Judy F.; Brzustowicz, Linda M.; Xing, Jinchuan
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 217-230. DOI: 10.1007/s00439-022-02496-z
        PubMed      DOI
    5.Profiling human pathogenic repeat expansion regions by synergistic and multi-level impacts on molecular connections

    Author: Fan, Cong; Chen, Ken; Wang, Yukai; Ball, Edward, V; Stenson, Peter D.; Mort, Matthew; Bacolla, Albino; Kehrer-Sawatzki, Hildegard; Tainer, John A.; Cooper, David N.; Zhao, Huiying
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 245-274. DOI: 10.1007/s00439-022-02500-6
        PubMed      DOI
    6.Identifying shared genetic factors underlying epilepsy and congenital heart disease in Europeans

    Author: Wu, Yiming; Bayrak, Cigdem Sevim; Dong, Bosi; He, Shixu; Stenson, Peter D.; Cooper, David N.; Itan, Yuval; Chen, Lei
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 275-288. DOI: 10.1007/s00439-022-02502-4
        PubMed      DOI
    7.Variations in mitochondrial DNA coding and d-loop region are associated with early embryonic development defects in infertile women

    Author: Liu, Yuqing; Zhao, Shuai; Chen, Xiaolei; Bian, Yuehong; Cao, Yongzhi; Xu, Peiwen; Zhang, Changming; Zhang, Jiangtao; Zhao, Shigang; Zhao, Han
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 193-200. DOI: 10.1007/s00439-022-02505-1
        PubMed      DOI
    8.Hearing of Otof-deficient mice restored by trans-splicing of N- and C-terminal otoferlin

    Author: Tang, Honghai; Wang, Hui; Wang, Shengyi; Hu, Shao Wei; Lv, Jun; Xun, Mengzhao; Gao, Kaiyu; Wang, Fang; Chen, Yuxin; Wang, Daqi; Wang, Wuqing; Li, Huawei; Shu, Yilai
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 2, pp. 289-304. DOI: 10.1007/s00439-022-02504-2
        PubMed      DOI
    9.Investigating the shared genetic architecture and causal relationship between pain and neuropsychiatric disorders

    Author: Chen, Mengya; Li, Si; Zhu, Ziwei; Dai, Chengguqiu; Hao, Xingjie
    Journal: HUMAN GENETICS. 2023; Vol. 142, Issue 3, pp. 431-443. DOI: 10.1007/s00439-022-02507-z
        PubMed      DOI
    10.Proteome-wide Mendelian randomization reveals the causal effects of immune-related plasma proteins on psychiatric disorders

    Author: Dang, Xinglun; Song, Meng; Lv, Luxian; Yang, Yongfeng; Luo, Xiong-Jian
    Journal: HUMAN GENETICS. 2023; Vol. , Issue , pp. -. DOI: 10.1007/s00439-023-02562-0
        PubMed      DOI
  • 同大类学科的其他著名期刊名称 h-index CiteScore
    NATURE REVIEWS MOLECULAR CELL BIOLOGY386164.40
    NATURE REVIEWS MICROBIOLOGY25060.20
    CELL705102.00
    NATURE METHODS25748.90
    NATURE BIOTECHNOLOGY39971.90
    CELL RESEARCH14341.80
    NATURE REVIEWS GENETICS32073.20
    Lancet Microbe022.90
    Cell Discovery1520.00
    NATURE GENETICS52753.80
    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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