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NEUROGENETICS 期刊收藏夹

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期刊名:   ISSN:   研究方向:   IF范围: -   SCI收录:
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NEUROGENETICS期刊基本信息Hello,您是该期刊的第24467位访客


基本信息 登录收藏
期刊名字NEUROGENETICSNEUROGENETICS

NEUROGENETICS
(此期刊被最新的JCR期刊SCIE收录)

LetPub评分
6.2
50人评分
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声誉
7.6

影响力
4.9

速度
7.0

期刊ISSN1364-6745
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E-ISSN1364-6753
2025-2026最新IF
(数据来源于网友提供)
注册登录后,查看IF
实时影响因子 截止2026年5月06日:1.61
2025-2026自引率6.2%点击查看自引率趋势图
五年IF
(数据来源于网友提供)
1.801数据由网友[轻盈爱吃]收集提供
h-index 56
CiteScore
2026年6月最新版
CiteScoreSJRSNIPCiteScore排名
2.400.7030.881
学科分区排名百分位
大类:Medicine
小类:Genetics (clinical)
Q372 / 100
大类:Medicine
小类:Genetics
Q4276 / 357
大类:Medicine
小类:Cellular and Molecular Neuroscience
Q486 / 102

期刊简介
Neurogenetics publishes findings that contribute to a better understanding of the genetic basis of normal and abnormal function of the nervous system. Neurogenetic disorders are the main focus of the journal. Neurogenetics therefore includes findings in humans and other organisms that help understand neurological disease mechanisms and publishes papers from many different fields such as biophysics, cell biology, human genetics, neuroanatomy, neurochemistry, neurology, neuropathology, neurosurgery and psychiatry.
All papers submitted to Neurogenetics should be of sufficient immediate importance to justify urgent publication. They should present new scientific results. Data merely confirming previously published findings are not acceptable.
期刊官方网站https://www.springer.com/10048
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此模板来自于期刊/出版社官网。开通VIP可免费下载,并享1w+期刊模板资源。
期刊投稿网址https://www.editorialmanager.com/nege/
作者指南网址https://www.springer.com/10048/submission-guidelines
该期刊中国学者近期发文 - NewInhibition of EIF2S1 expression regulates the PI3K/AKT pathway to mediate apoptosis in glioma cells: an in vitro study
Author: Li, Gang; Wang, Min; Wei, Na; Qiu, Zheng
Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00911-5


Clinical and genetic characteristics of CSF1R-related leukoencephalopathy: a retrospective analysis of three cases
Author: Xie, Sifen; Yang, Qiqiong; Pan, Mengqiu; Hu, Yepeng; Huang, Nayang; Chen, Zhongjie; Ye, Jinlong; Luo, Sheng; Wang, Zhanhang; Kuang, Zuying
Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00907-1


Mechanism of the N87D mutation in SOD1-atypical amyotrophic lateral sclerosis case report and literature review molecular mechanism of N87D mutation in SOD1
Author: Pi, Chenghui; Liu, Yang; Jia, Zhihua; Zhang, Mingjie; Wang, Xiaolin; Zhao, He; Dong, Zhao; Yu, Shengyuan; Liu, Ruozhuo
Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00909-z


Homozygous NOTCH3 c.3373G > A (p.(Glu1125Lys)) in a consanguineous Chinese family presenting with vestibular migraine and epilepsy: Expanding the genotype-phenotype spectrum
Author: Luo, Yong; Chen, Jian; Li, Qian; Zhang, Yun
Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00899-y


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NEUROGENETICS的语言要求,还能让NEUROGENETICS编辑和审稿人得到更好的审稿体验,让稿件最大限度地被NEUROGENETICS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
涉及的研究方向医学-临床神经学
出版国家或地区GERMANY
出版语言English
出版周期Quarterly
出版年份1997
年文章数 72点击查看年文章数趋势图
Gold OA文章占比17.42%
研究类文章占比:
文章 ÷(文章 + 综述)
81.94%
WOS期刊JCR分区
2025-2026年最新版
注册登录后,查看WOS分区等级
期刊分区表预警名单 2026年03月发布的新锐学术版:不在预警名单中

2025年03月发布的2025版:不在预警名单中

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
《新锐期刊分区表》
2026年3月发布
点击查看期刊分区表趋势图
大类学科小类学科Top期刊综述期刊
医学 1区4区3区
GENETICS & HEREDITY
遗传学
2区3区4区
CLINICAL NEUROLOGY
临床神经病学
2区4区4区
N/A
期刊分区表
2025年3月升级版
大类学科小类学科Top期刊综述期刊
医学 4区4区3区
CLINICAL NEUROLOGY
临床神经病学
1区4区4区
GENETICS & HEREDITY
遗传学
1区3区4区
期刊分区表
2023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 1区4区4区
CLINICAL NEUROLOGY
临床神经病学
4区4区4区
GENETICS & HEREDITY
遗传学
4区1区4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=1364-6745%5BISSN%5D
平均审稿速度网友分享经验:
平均6月
平均录用比例网友分享经验:
约95%
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NEUROGENETICS顺利发表。
快看看作者怎么说吧:服务好评 论文致谢
提交文稿
期刊常用信息链接
同领域相关期刊 NEUROGENETICS期刊近年CiteScore指标趋势图
该杂志的自引率趋势图 NEUROGENETICS期刊分区表趋势图
该杂志的年文章数趋势图 同领域作者分享投稿经验
NEUROGENETICS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
  • 期刊分区表趋势图
  • 年文章数趋势图
  • 该期刊中国学者近期发文
  • 期刊分区表相关期刊
  • 同类著名期刊名称 h-index CiteScore
    LANCET NEUROLOGY25975.00
    Nature Reviews Neurology12433.10
    NEURO-ONCOLOGY10521.10
    Alzheimers & Dementia9413.90
    BRAIN30821.20
    SLEEP MEDICINE REVIEWS12221.10
    STROKE29213.10
    Brain Stimulation6412.80
    NEUROLOGY3319.50
    JOURNAL OF HEADACHE AND PAIN5011.90
    期刊分区表同大类学科的热搜期刊 浏览次数
    MEDICINE916453
    JOURNAL OF ETHNOPHARMACOLOGY817640
    Frontiers in Immunology767391
    BIOMEDICINE & PHARMACOTHERAPY737942
    Frontiers in Pharmacology732757
    BIOMATERIALS726469
    PHYTOMEDICINE661657
    Frontiers in Oncology632557
    Biomedical Signal Processing and Control619658
    IEEE Journal of Biomedical and Health Informatics613061
  •  

    NEUROGENETICS NEUROGENETICS
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    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.Inhibition of EIF2S1 expression regulates the PI3K/AKT pathway to mediate apoptosis in glioma cells: an in vitro study

    Author: Li, Gang; Wang, Min; Wei, Na; Qiu, Zheng
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00911-5
        PubMed      DOI
    2.Clinical and genetic characteristics of CSF1R-related leukoencephalopathy: a retrospective analysis of three cases

    Author: Xie, Sifen; Yang, Qiqiong; Pan, Mengqiu; Hu, Yepeng; Huang, Nayang; Chen, Zhongjie; Ye, Jinlong; Luo, Sheng; Wang, Zhanhang; Kuang, Zuying
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00907-1
        PubMed      DOI
    3.Mechanism of the N87D mutation in SOD1-atypical amyotrophic lateral sclerosis case report and literature review molecular mechanism of N87D mutation in SOD1

    Author: Pi, Chenghui; Liu, Yang; Jia, Zhihua; Zhang, Mingjie; Wang, Xiaolin; Zhao, He; Dong, Zhao; Yu, Shengyuan; Liu, Ruozhuo
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00909-z
        PubMed      DOI
    4.Homozygous NOTCH3 c.3373G > A (p.(Glu1125Lys)) in a consanguineous Chinese family presenting with vestibular migraine and epilepsy: Expanding the genotype-phenotype spectrum

    Author: Luo, Yong; Chen, Jian; Li, Qian; Zhang, Yun
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00899-y
        PubMed      DOI
    5.Neuroepigenetic regulation by long non-coding RNAs in sepsis-associated encephalopathy: cell-type programs and translational biomarkers

    Author: Wang, Yun; Li, Xuexin; Sun, Bowen; He, Fei; Liu, Li
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00889-0
        PubMed      DOI
    6.Expanding mutational and phenotypic spectrum of CST3-related leukoencephalopathy: a novel family and literature review

    Author: Zhong, Shaoping; Lian, Yangye; Liang, Jingzhen; Wang, Shuyang; Zhang, Qianqian; Liu, Jianying; Ding, Jing
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00898-z
        PubMed      DOI
    7.Thorough evaluation of a novel splice variant in a female patient with MED12-related intellectual disability

    Author: Tang, Hongmei; Han, Mingshan; Luo, Jie; Zhao, Xiuying; Gao, Ting; Li, Jinling; Zhang, Jing; He, Lu; Li, Zhibin; Huang, Mingwei; Xu, Kaishou
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00894-3
        PubMed      DOI
    8.Aberrant RNA splicing caused by variant in DEPDC5 identified in a patient with pharmacoresistant epilepsy

    Author: Zhou, Cong; Wei, Xing; Xiang, Qinqin; Mai, Jingqun; Wang, Jing
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00890-7
        PubMed      DOI
    9.Association of TRPM7 gene mutation with familial vestibular migraine

    Author: Luo, Yong; Chen, Jian; Li, Qian; Zhang, Yun
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00886-3
        PubMed      DOI
    10.A novel heterozygous mutation of BCL11B gene causes neurodevelopmental disorder and middle type hypospadias in a Chinese boy with 5 years follow-up

    Author: Liu, Yawen; Pan, Zhen; Shi, Jiarui; Jiang, Mingyan; Li, Jinrong
    Journal: NEUROGENETICS. 2026; Vol. 27, Issue 1, pp. -. DOI: 10.1007/s10048-026-00880-9
        PubMed      DOI
  • 同大类学科的其他著名期刊名称 h-index CiteScore
    CA-A CANCER JOURNAL FOR CLINICIANS144649.80
    LANCET70092.40
    MMWR Surveillance Summaries093.20
    Nature Reviews Clinical Oncology127126.60
    NATURE REVIEWS DRUG DISCOVERY289159.20
    NEW ENGLAND JOURNAL OF MEDICINE93374.80
    Signal Transduction and Targeted Therapy081.60
    ANNALS OF ONCOLOGY21069.60
    Nature Reviews Disease Primers4871.30
    World Psychiatry6184.80
    同分区等级的其他期刊名称 h-index CiteScore
    BRITISH JOURNAL OF BIOMEDICAL SCIENCE4012.70
    Cancer Genetics355.50
    GetMobile-Mobile Computing & Communications Review00.00
    MedComm - Oncology05.30
    Bulletin of the Peabody Museum of Natural History136.80
    Life Medicine06.10
    JBI Evidence Synthesis08.00
    SEMINARS IN ONCOLOGY1254.90
    Turkish Journal of Emergency Medicine05.90
    Cancer Pathogenesis and Therapy06.20
以上SCI期刊相关数据和信息来源于网络,仅供参考。
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