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Human Genomics

Human Genomics杂志,由BioMed Central出版,于2003年创刊,1 issue/year,出版语言English,ISSN:1473-9542,E-ISSN:1479-7364。

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Human Genomics
Human Genomics
Human Genomics
SCI SCIE

杂志介绍

JCR分区
Q2
中科院分区
2区
影响因子
4.1
CiteScore
6.4
期刊收录
SCI、SCIE

Human Genomics(中文译名:《人类基因组学》),ISSN:1473-9542,EISSN:1479-7364,是BioMed Central出版的国际性学术期刊,创刊于2003年,以1 issue/year形式稳定发行,2026年总发文量约169篇。该刊采用OA开放访问,学科归属为GENETICS & HEREDITY。该刊是医学、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4.1,2025年期刊CiteScore为6.4,2025年期刊自引率约0%,在中科院期刊分区体系中位列医学大类2区,在所属学科领域具备高学术影响力与国际认可度。Human Genomics长期聚焦医学、遗传学及相关产业的技术应用前沿,平均审稿周期11 Weeks,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,重点收录能够对医学、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,USACHINA MAINLAND、Japan、Australia、England、Italy、Canada等为核心发文国家与地区;RIKENYALE UNIVERSITY、HARVARD UNIVERSITY、UNIVERSITY OF CALIFORNIA SYSTEM、UNIVERSITY OF QUEENSLAND、UNIVERSITY OF TOKYO、INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)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
医学
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
医学
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
医学
3区
GENETICS & HEREDITY 遗传学
3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 49 / 192

74.7

学科:GENETICS & HEREDITY SCIE Q1 40 / 192

79.43

2023-2024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 49 / 191

74.6

学科:GENETICS & HEREDITY SCIE Q2 50 / 191

74.08


中国学者近期发文

1
Cross-trait genomic and sequential analyses of multiple omics datasets identified shared genetic components for the gut-eye axi

Author:Gao, Yuelan; Xu, Jianming; Yu, Jun; Wang, Yuyao; Zhang, Yuzhou; Kam, Ka Wai; Ho, Mary; Young, Alvin L.; Pang, Chi Pui; Tham, Clement C.; Yam, Jason C.; Chen, Li Jia

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00947-6

2
Phenotypic spectrum of 11p15.5 duplications: parent-of-origin and copy number variant size shape outcomes from Silver-Russell to Beckwith-Wiedemann syndrome

Author:Wang, Chenyang; Zhang, Hengyuan; Wang, Meiying; Gao, Juan; Lv, Yibing; Huang, Jianmei; Pan, Shuxian; Wu, Dong; Kang, Bing; Hou, Qiaofang; Liao, Shixiu

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00942-x

3
A cross-scale multimodal framework identifies clinically actionable immunotherapy biomarkers in melanoma through bulk to single-cell and spatial transcriptomics integratio

Author:Huoshen, Wuda; Yuan, Kun; Xiong, Junkai; Lin, Yilong; Yu, Wenjie; Xie, Yun; Yuan, Qian; Zhang, Xinyue; Dong, Changqing; Sun, Chen; Yi, Sha

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00919-w

4
Unraveling the potential carcinogenic risk of bisphenols: a comprehensive network analysis and computational toxicology insight

Author:Li, Tiegang; Yan, Zheng; Zhao, Wenyi; Hou, Yufang; Lv, Silin; Zeng, Zifan; Yang, Liu; Zhou, Mingxuan; Zhang, Fang; Ren, Xinyi; Zhou, Yixin; Zhu, Zengni; Huang, Siying; Yang, Min

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00948-5

5
A comprehensive analysis of the interaction network of immunomodulatory-related differentially expressed genes, aiming to identify biomarkers associated with Parkinson's diseas

Author:Gao, Jianying

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00929-8

6
Leveraging proteomics and machine learning for mechanism and biomarker discovery on glioma progression and transformation: from LGG to GB

Author:Huang, Qinhong; Liang, Hui; Liu, Jie; Shi, Shenbao; Sun, Xinlin; Ke, Yiquan; Chen, Taoliang

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00945-8

7
Carrier rates for recessive monogenic diseases in the Chinese Han population: a systematic revie

Author:Xia, Yirong; Ma, Yinan

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00940-z

8
A pan-cancer analysis of the oncogenic and immunological roles of RGS5 in clear cell renal cell carcinomas based on in vitro experiment validation (vol 19, 14, 2025

Author:Zhang, Ying; Wang, Huming; Dai, Fang; He, Ke; Tuo, Zhouting; Wang, Jinyou; Bi, Liangkuan; Chen, Xin

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00938-7

9
Challenges in functional validation and mechanistic interpretation of a novel LACC1 variant in familial juvenile arthriti

Author:Yu, Lin; Yang, Dujiang; Ye, Zhijun; Wang, Guoyou

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-025-00865-z

10
Therapeutic rewiring of ceRNA networks: a computational pipeline for drug repurposing in acute kidney injury via circRNA-miRNA-mRNA axis disruptio

Author:Wang, Ming; Gao, Feng

Journal: HUMAN GENOMICS. 2026; Vol. 20, Issue 1, pp. -. DOI: 10.1186/s40246-026-00930-1


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Human Genomics

国际简称:HUM GENOMICS参考译名:人类基因组学

年发文量:169 CiteScore:6.4 是否预警:否 Gold OA文章占比:100.00% 研究类文章占比:89.35%

杂志社联系方式:CAMPUS, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW

Human Genomics