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Human Genetics

Human Genetics杂志,由Springer Berlin Heidelberg出版,于1964年创刊,Monthly,出版语言English,ISSN:0340-6717,E-ISSN:1432-1203。

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Human Genetics
Human Genetics
Human Genetics
SCI SCIE

杂志介绍

JCR分区
Q2
中科院分区
2区
影响因子
3.4
CiteScore
8.7
期刊收录
SCI、SCIE

Human Genetics(中文译名:《人类遗传学》),ISSN:0340-6717,EISSN:1432-1203,是Springer Berlin Heidelberg出版的国际性学术期刊,创刊于1964年,以Monthly形式稳定发行,2026年总发文量约72篇。该刊采用非OA开放访问,学科归属为生物 - 遗传学。该刊是生物、遗传学领域的国际权威刊物,已被SCI(科学引文索引)、SCIE(科学引文索引扩展版)等国际主流学术数据库收录。2026年期刊影响因子达3.4,2025年期刊CiteScore为8.7,2025年期刊自引率约2.9%,在中科院期刊分区体系中位列生物学大类2区,在所属学科领域具备高学术影响力与国际认可度。Human Genetics长期聚焦生物、遗传学及相关产业的技术应用前沿,平均审稿周期约1月,审稿流程高效稳定。在稿件录用评判中,该刊将创新性与前沿性作为核心遴选标准,重点收录能够对生物、遗传学领域的落地与发展产生实质性推动价值的研究成果。

从全球发文格局来看,USAEngland、France、CHINA MAINLAND、GERMANY (FED REP GER)、Canada、Italy等为核心发文国家与地区;INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)HARVARD UNIVERSITY、UNIVERSITY OF CALIFORNIA SYSTEM、UNIVERSITE DE PARIS、UNIVERSITY OF LONDON、BAYLOR COLLEGE OF MEDICINE、BRIGHAM & WOMEN'S HOSPITAL等高校与科研机构是期刊的主要发文单位。

期刊评价

名词解释:

影响因子(Impact Factor, IF):指该期刊前两年发表的文章,在第三年的平均被引用次数。它反映了期刊的近期平均影响力和热度。

中科院分区:中科院分区表是国内主流的学术期刊分级评价工具,核心意义是建立跨学科可比的统一评价标尺,为职称评审、学位授予、科研立项等科研管理工作提供标准化量化依据,同时帮助科研人员筛选优质期刊、规避学术风险,适配国内本土化的科研评价需求。

期刊分区表

《新锐期刊分区表》(2026年3月发布)

大类学科 小类学科 Top期刊 综述期刊
生物学
2区
GENETICS & HEREDITY 遗传学
2区

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
生物学
2区
GENETICS & HEREDITY 遗传学
2区

期刊分区表(2023年12月升级版)

大类学科 小类学科 Top期刊 综述期刊
生物学
2区
GENETICS & HEREDITY 遗传学
2区

JCR分区

2025-2026年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:GENETICS & HEREDITY SCIE Q2 67 / 192

65.4

学科:GENETICS & HEREDITY SCIE Q2 65 / 192

66.41

2024-2025年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:GENETICS & HEREDITY SCIE Q2 56 / 192

71.1

学科:GENETICS & HEREDITY SCIE Q2 58 / 192

70.05


中国学者近期发文

1
Epigenetic silencing of DLEC1 correlates with tumor immune microenvironment and predicts immunotherapy prognosis in multiple cancer

Author:Ming, Ruijie; Xiong, Qi; Tan, Shuh-Ying; Li, Lili; Bao, Shujie; Wang, Jianhua; Zhao, Lijuan; He, Xiaoqian; Zheng, Zeze; Wang, Yan; Liu, Xiaoyu; Tang, Jun; Wu, Zhongjun; Xiang, Tingxiu; Tao, Qian

Journal: HUMAN GENETICS. 2026; Vol. 145, Issue 1, pp. -. DOI: 10.1007/s00439-026-02828-3

2
Integrating machine learning and spatial transcriptomics uncovers shared immunomodulatory deubiquitinases in MAFLD and HC

Author:Han, Yu-xi; Li, Hongze; Xia, Wendi; Ma, Junyi; Zhang, Jiaqi; Li, Yiling

Journal: HUMAN GENETICS. 2026; Vol. 145, Issue 1, pp. -. DOI: 10.1007/s00439-026-02833-6

3
Human YTHDC2 mutations disturb RNA homeostasis of oocytes and early embryo

Author:Su, Wei; Wang, Yang; Sun, Jiaqi; Zhang, Changlong; Yin, Changjian; Cui, Ying; Chen, Xiaolei; Yang, Bohan; Zhao, Shigang; Wu, Keliang; Lin, Ge; Chen, Zi-Jiang; Zheng, Wei; Zhang, Honghui; Zhao, Han

Journal: HUMAN GENETICS. 2026; Vol. 145, Issue 1, pp. -. DOI: 10.1007/s00439-026-02818-5

4
Higher mitochondrial DNA methylation is associated with increased risk of stroke: a nested case-control stud

Author:Fu, Xueru; Fang, Yuewan; Zhao, Yujie; Yang, Bin; Su, Yaqin; Yang, Li; Huo, Weifeng; Wen, Liuding; Wu, Yuying; Zhao, Yang; Hu, Fulan; Zhang, Ming; Wen, Hongwei; Yin, Lei; Hu, Dongsheng; Chen, Chuande

Journal: HUMAN GENETICS. 2026; Vol. 145, Issue 1, pp. -. DOI: 10.1007/s00439-026-02823-8

5
Clinical characteristics and genetic variant spectrum of 27 patients with coagulation factor XI deficienc

Author:Ren, Juan; Yu, Yalin; Wang, Duanyang; Fang, Shuai; Chen, Xiuhua; Hao, Lixia; Zhao, Jiaoyu; Wang, Lei; Yang, Linhua; Wang, Gang

Journal: HUMAN GENETICS. 2026; Vol. 145, Issue 1, pp. -. DOI: 10.1007/s00439-026-02819-4

6
Profiling structural variations of the α-globin gene cluster by the single molecule real-time sequencing: remarkable diversity of the spectrum with rare and novel variants identified in a large Chinese cohor

Author:Wei, Dan; Cheng, Zifeng; Wei, Wei; Gui, Chunrong; Liu, Juliang; Chen, Hongfei; Ma, Yunting; Peng, XianWei; Yu, Dan; Huang, Yan; Lai, Yinghui; Gui, Baoheng

Journal: HUMAN GENETICS. 2026; Vol. 145, Issue 1, pp. -. DOI: 10.1007/s00439-025-02801-6

7
Accelerating genetic diagnostics in retinitis pigmentosa: implementation of a semi-automated bespoke cohort analysis workflow for Hong Kong Genome Projec

Author:Ying, Dingge; Kwok, Jamie Sui Lam; Chu, Annie Tsz Wai; Ma, Wei; Tam, Helen Ying Fung; Or, Dicky; Hue, Shirley Pik Ying; Li, Qing; Leung, Christopher Kai Shun; Chung, Brian Hon Yin

Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 5, pp. 515-528. DOI: 10.1007/s00439-025-02737-x

8
Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain developmen

Author:Chen, Bo; Zhang, Chenyang; Rui, Huanwen; Shen, Dan; Huang, Zhuxi; Feng, Weijun

Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 5, pp. 529-543. DOI: 10.1007/s00439-025-02740-2

9
Comprehensive profiling of tsRNAs in acute coronary syndrome: expression patterns, clinical correlations, and functional insight

Author:He, Yi; Wang, Jing; Chen, Chen; Wang, Rongli; Ma, Xiaozhu; Ma, Ruiying; Sun, Yang; Wang, Luyun; Ding, Hu

Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 5, pp. 575-590. DOI: 10.1007/s00439-025-02742-0

10
Predicting the impact of rare variants on RNA splicing in CAGI

Author:Lord, Jenny; Oquendo, Carolina Jaramillo; Wai, Htoo A.; Douglas, Andrew G. L.; Bunyan, David J.; Wang, Yaqiong; Hu, Zhiqiang; Zeng, Zishuo; Danis, Daniel; Katsonis, Panagiotis; Williams, Amanda; Lichtarge, Olivier; Chang, Yuchen; Bagnall, Richard D.; Mount, Stephen M.; Matthiasardottir, Brynja; Lin, Chiaofeng; Hansen, Thomas van Overeem; Leman, Raphael; Martins, Alexandra; Houdayer, Claude; Krieger, Sophie; Bakolitsa, Constantina; Peng, Yisu; Kamandula, Akash; Radivojac, Predrag; Baralle, Diana

Journal: HUMAN GENETICS. 2025; Vol. 144, Issue 2-3, pp. 243-251. DOI: 10.1007/s00439-023-02624-3


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Human Genetics

国际简称:HUM GENET参考译名:人类遗传学

年发文量:72 CiteScore:8.7 是否预警:否 Gold OA文章占比:48.89% 研究类文章占比:86.11%

杂志社联系方式:SPRINGER, 233 SPRING ST, NEW YORK, USA, NY, 10013

Human Genetics