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Journal Of Human Genetics

Journal Of Human Genetics杂志,由Springer Nature出版,于1977年创刊,Monthly,出版语言English,ISSN:1434-5161,E-ISSN:1435-232X。

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Journal Of Human Genetics
Journal Of Human Genetics
Journal Of Human Genetics
SCI SCIE

杂志介绍

JCR分区
Q3
中科院分区
3区
影响因子
2.3
CiteScore
5.1
期刊收录
SCI、SCIE

Journal Of Human Genetics(中文译名:《人类遗传学杂志》),ISSN:1434-5161,EISSN:1435-232X,是Springer Nature出版的国际性学术期刊,创刊于1977年,以Monthly形式稳定发行,2026年总发文量约120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2.3,2025年期刊CiteScore为5.1,2025年期刊自引率约4.3%,在中科院期刊分区体系中位列生物学大类3区,在所属学科领域具备高学术影响力与国际认可度。Journal Of Human Genetics长期聚焦生物、遗传学及相关产业的技术应用前沿,平均审稿周期偏慢,4-8周,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,JapanCHINA MAINLAND、USA、England、South Korea、GERMANY (FED REP GER)、India等为核心发文国家与地区;YOKOHAMA CITY UNIVERSITYUNIVERSITY OF TOKYO、RIKEN、NATIONAL CENTER FOR CHILD HEALTH & DEVELOPMENT - JAPAN、KYOTO UNIVERSITY、TOKYO MEDICAL & DENTAL UNIVERSITY (TMDU)、CHIBA UNIVERSITY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
3区
GENETICS & HEREDITY 遗传学
3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
3区
GENETICS & HEREDITY 遗传学
3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
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 Q3 114 / 192

40.9

学科:GENETICS & HEREDITY SCIE Q3 109 / 192

43.49

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 95 / 192

50.8

学科:GENETICS & HEREDITY SCIE Q3 99 / 192

48.7


中国学者近期发文

1
SMN1 mutation spectrum and functional analysis of novel SMN1 variants in a Chinese spinal muscular atrophy cohor

Author:Li, Gui-He; Wu, Li-Wen; Li, Jing; Dong, Sen-Wei; Hong, Jing-Mei; Xie, Ying-Xuan; Sun, Yu-Hao; He, Jin; Wang, Ning; Chen, Wan-Jin; Chen, Hai-Zhu

Journal: JOURNAL OF HUMAN GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1038/s10038-026-01473-y

2
Interaction between human oxoguanine glycosylase 1 gene polymorphisms and smoking status on nasopharyngeal carcinoma ris

Author:Peng, Fanyu; Zhang, Ruru; Yu, Rong; Wu, Jing; Wang, Lijun; Liu, Yatian; Liu, Delin; Yan, Pengwei; Yang, Baixia

Journal: JOURNAL OF HUMAN GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1038/s10038-026-01468-9

3
Vacuolar myopathy caused by CASQ1 p.Asp244His: pathogenic evidence from two unrelated Chinese familie

Author:Xia, Xingyu; Laarne, Milla; Pan, Tonglin; Jiao, Kexin; Cheng, Nachuan; Zhu, Bochen; Diao, Meining; Gao, Mingshi; Liu, Ying; Zhao, Chongbo; Zhao, Zhe; Zhu, Wenhua

Journal: JOURNAL OF HUMAN GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1038/s10038-026-01461-2

4
A case report of spinocerebellar ataxia with TRPC3 gene mutation and review of literatur

Author:Liu, Yueying; Xie, Miaoxian; Liu, Fang; Chen, Haibo; Su, Wen; Ma, Xinxin

Journal: JOURNAL OF HUMAN GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1038/s10038-025-01449-4

5
Novel susceptibility gene SLC23A2 functions via PI3K-AKT-mTOR pathway in etiology of non-syndromic cleft palat

Author:Yin, Bin; Li, Mu-Jia; Sun, Jia-Lin; You, Yue; Zhang, Si-Di; Wan, Qian-Xue; Yao, Mei-Lin; Yang, Cheng-Wei; Sun, Hua-Qin; Lin, Zi-Yuan; Shi, Bing; Jia, Zhong-Lin

Journal: JOURNAL OF HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1038/s10038-025-01352-y

6
The prevalence of laterality defects in patients with congenital heart diseas

Author:Xie, Xiao-hui; Gu, Heng; Yuan, Zhuang-zhuang; Yang, Jun-lin; Qin, Ke-le; Chen, Jin-lan; Zhang, Wei-zhi; Xie, Li; Yang, Yi-feng; Tan, Zhi-ping

Journal: JOURNAL OF HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1038/s10038-025-01351-z

7
Microcephaly-related global developmental delay caused by a pathogenic METTL5 splicing mutation in a Chinese famil

Author:Zhou, Xiaoyan; Teng, Congcong; Zhao, Wenjing; Yang, Wen; Yang, Yuecheng; Chen, Qing; He, Ming; Zhang, Jie

Journal: JOURNAL OF HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1038/s10038-025-01354-w

8
Reclassification of variants of uncertain significance in neonatal genetic diseases: implications from a clinician's perspectiv

Author:Wu, Xiaojiao; Jiao, Jiancheng; Pu, Weicong; Yan, Xiaotong; Xia, Yaofang; Guo, Weiwei; Ma, Li; Cao, Yanyan

Journal: JOURNAL OF HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1038/s10038-025-01348-8

9
Bi-allelic KCTD19 variants associated with meiotic arrest and non-obstructive azoospermia in human

Author:Xu, Shuai; Zhang, Chenwang; Yao, Chencheng; Ni, Wanze; Qian, Dewei; Meng, Zizhou; Sun, Yifan; Deng, Cunzhong; Bai, Furong; Zhang, Jianxiong; Li, Peng; Huang, Yuhua; Zhou, Zhi; Li, Zheng; Li, Na; Zhang, Yuxiang

Journal: JOURNAL OF HUMAN GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1038/s10038-025-01350-0


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Journal Of Human Genetics

国际简称:J HUM GENET参考译名:人类遗传学杂志

年发文量:120 CiteScore:5.1 是否预警:否 Gold OA文章占比:23.20% 研究类文章占比:79.17%

杂志社联系方式:NATURE PUBLISHING GROUP, 75 VARICK ST, 9TH FLR, NEW YORK, USA, NY, 10013-1917

Journal Of Human Genetics