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Human Molecular Genetics

Human Molecular Genetics杂志,由Oxford University Press出版,于1992年创刊,Semimonthly,出版语言English,ISSN:0964-6906,E-ISSN:1460-2083。

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Human Molecular Genetics
Human Molecular Genetics
Human Molecular Genetics
SCI SCIE

杂志介绍

JCR分区
Q2
中科院分区
2区
影响因子
3.1
CiteScore
7.2
期刊收录
SCI、SCIE

Human Molecular Genetics(中文译名:《人类分子遗传学》),ISSN:0964-6906,EISSN:1460-2083,是Oxford University Press出版的国际性学术期刊,创刊于1992年,以Semimonthly形式稳定发行,2026年总发文量约182篇。该刊采用非OA开放访问,学科归属为生物 - 生化与分子生物学。该刊是生物、生化与分子生物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3.1,2025年期刊CiteScore为7.2,2025年期刊自引率约0%,在中科院期刊分区体系中位列生物学大类2区TOP 期刊,在所属学科领域具备高学术影响力与国际认可度。Human Molecular Genetics长期聚焦生物、生化与分子生物学及相关产业的技术应用前沿,平均审稿周期较快,2-4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、生化与分子生物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、GERMANY (FED REP GER)、France、Italy、Canada、CHINA MAINLAND等为核心发文国家与地区;UNIVERSITY OF LONDONUNIVERSITY OF CALIFORNIA SYSTEM、HARVARD UNIVERSITY、INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)、CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS)、UNIVERSITY OF OXFORD、UNIVERSITE DE PARIS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
BIOCHEMISTRY & MOLECULAR BIOLOGY 生化与分子生物学 GENETICS & HEREDITY 遗传学
2区 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
BIOCHEMISTRY & MOLECULAR BIOLOGY 生化与分子生物学 GENETICS & HEREDITY 遗传学
3区 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
2区
BIOCHEMISTRY & MOLECULAR BIOLOGY 生化与分子生物学 GENETICS & HEREDITY 遗传学
3区 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:BIOCHEMISTRY & MOLECULAR BIOLOGY SCIE Q3 192 / 328

41.6

学科:GENETICS & HEREDITY SCIE Q2 74 / 192

61.7

学科:BIOCHEMISTRY & MOLECULAR BIOLOGY SCIE Q2 123 / 328

62.65

学科:GENETICS & HEREDITY SCIE Q2 80 / 192

58.59

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:BIOCHEMISTRY & MOLECULAR BIOLOGY SCIE Q2 151 / 320

53

学科:GENETICS & HEREDITY SCIE Q2 66 / 192

65.9

学科:BIOCHEMISTRY & MOLECULAR BIOLOGY SCIE Q2 111 / 321

65.58

学科:GENETICS & HEREDITY SCIE Q2 72 / 192

62.76


中国学者近期发文

1
An Alu mediated intergenic inversion in RBCK1 causing Polyglucosan body myopathy type

Author:Zhu, Bochen; Jiao, Kexin; Luo, Xiaona; Gao, Mingshi; Yue, Dongyue; Zhang, Jialong; Xia, Xingyu; Zhang, Yuanfeng; Zhao, Chongbo; Hedberg-Oldfors, Carola; Oldfors, Anders; Chen, Xuqin; Zhu, Wenhua

Journal: HUMAN MOLECULAR GENETICS. 2026; Vol. 35, Issue 4, pp. -. DOI: 10.1093/hmg/ddag009

2
Correlations between phenotype and gene region-specific episignatures in Rubinstein-Taybi syndrome and Menke-Hennekam syndrom

Author:Tang, Yanan; Ye, Xiantao; Zhan, Yongkun; Zhang, Kaichuang; Qiu, Wenjuan; Yang, WenQing; Gu, Xuefan; Yu, Yongguo; Xiao, Bing; Sun, Yu

Journal: HUMAN MOLECULAR GENETICS. 2026; Vol. 35, Issue 5, pp. -. DOI: 10.1093/hmg/ddag006

3
Heterozygous loss-of-function variant in METTL5 is associated with intellectual disabilit

Author:Tao, Wenjun; Ying, Yanqin; Sun, Jiaju; Wu, Yuxin; Jiang, Xinhui; Zhang, Jun; Zhou, Jun

Journal: HUMAN MOLECULAR GENETICS. 2026; Vol. 35, Issue 6, pp. -. DOI: 10.1093/hmg/ddag018

4
A reanalysis of a genome-wide association study on breast cancer in Asian populations using the SG10K_Health reference panel for imputation: a multi-Centre case-control analysi

Author:Chang, Xuling; Mariapun, Shivaani; Li, Mengyu; Wang, Ling; Ho, Peh Joo; Khng, Alexis Jiaying; Muir, Kenneth R.; Lophatananon, Artitaya; Aronson, Kristan J.; Murphy, Rachel A.; Kwong, Ava; Au, Chun Hang; Kim, Sung-Won; Park, Sue K.; Stram, Daniel O.; Wu, Anna H.; Teo, Soo-Hwang; Yip, Cheng-Har; Tai, Nur Aishah Mohd; John, Esther M.; Kurian, Allison W.; Iwasaki, Motoki; Yamaji, Taiki; Choi, Ji-Yeob; Kang, Daehee; Shu, Xiao-Ou; Zheng, Wei; Hartman, Mikael; Tan, Ern Yu; Tan, Veronique Kiak-Mien; Lim, Geok Hoon; Bolla, Manjeet K.; Dunning, Alison M.; Dennis, Joe; Wang, Qin; Naven, Marc; Easton, Douglas F.; Dorajoo, Rajkumar; Ho, Weang-Kee; Li, Jingmei

Journal: HUMAN MOLECULAR GENETICS. 2026; Vol. 35, Issue 6, pp. -. DOI: 10.1093/hmg/ddag015

5
Simultaneous detection of small and large variants enhances the diagnosis of rare diseases using full genome sequencin

Author:Tsai, Meng-Ju Melody; Kao, Hsiao-Jung; Wei, Chun-Yu; Chen, Hsiao-Huei; Chou, Yen-Yin; Hung, Miao-Zi; Hsueh, Hsueh-Wen; Hsieh, Sung-Tsang; Fan, Pi-Chuan; Tu, Yi-Fang; Lin, Ju-Li; Chen, Hui-An; Hsu, Rai-Hseng; Chien, Yin-Hsiu; Hwu, Wuh-Liang; Kwok, Pui-Yan; Lee, Ni-Chung

Journal: HUMAN MOLECULAR GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf204

6
COQ8B gene deficiency as a potential cause of retinal abnormalities in Pediatric kidney transplant recipient

Author:Feng, Yonghua; Feng, Yi; Wang, Zhigang; Li, Wenjing; Zhu, Haowei; Li, Zhou; Feng, Chenghao; Xu, Hongen; Feng, Guiwen; Zhang, Di; Shang, Wenjun

Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf084

7
De novo missense variants of KCNA3, KCNA4, and KCNA6 cause early onset developmental epileptic encephalopath

Author:Tsai, Meng-Han; Lo, Chia-Hua; Liu, You-Xuan; Wu, Sheng-Nan; Kuo, Cheng-Yen; Liu, Yi-Hsuan; Chang, Ying-Chao; Lin, Kuan-Lin; Hung, Po-Cheng; Chen, Hwei-Hsien; Chen, Jian-Liang; Yao, Chi-Kuang; Hwang, Eric; Wang, Ya-Jean

Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf090

8
Calcium homeostasis modulator 2 aggravates α-synuclein-induced neurotoxicity in Parkinson's disease by activating PARP-1 depended Parthanato

Author:Pan, Qi; Xu, Huanjun; Xiao, Zongyu; Liu, Guanghao; Zhang, Huaming; Li, Yiying

Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf091

9
Linking DNA methylation in brain regions to Alzheimer's disease risk: a Mendelian randomization stud

Author:Zhong, Hua; Zhu, Jingjing; Liu, Shuai; Zhou, Dan; Long, Quan; Wu, Chong; Zhao, Bingxin; Cheng, Chao; Yang, Yaohua; Wu, Qing; Wu, Yong; Li, Changwei; Wang, Zhaoming; Wu, Jianyong; Guo, Xingyi; Zhi, Degui; Deng, Youping; Wu, Lang

Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf053

10
Genetic characteristics associated with isolated Microtia revealed through whole exome sequencing of 201 pedigree

Author:Wu, Siyi; Chen, Xin; Chen, Ying; Li, Chenlong; Yang, Run; Zhang, Tianyu; Ma, Jing

Journal: HUMAN MOLECULAR GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1093/hmg/ddaf063


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Human Molecular Genetics

国际简称:HUM MOL GENET参考译名:人类分子遗传学

年发文量:182 CiteScore:7.2 是否预警:否 Gold OA文章占比:42.52% 研究类文章占比:89.56%

杂志社联系方式:OXFORD UNIV PRESS, GREAT CLARENDON ST, OXFORD, ENGLAND, OX2 6DP

Human Molecular Genetics