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Molecular Genetics & Genomic Medicine

Molecular Genetics & Genomic Medicine杂志,由John Wiley and Sons Inc.出版,于2013年创刊,6 issues/year,出版语言English,ISSN:2324-9269,E-ISSN:2324-9269。

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Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
SCI SCIE

杂志介绍

JCR分区
Q4
中科院分区
4区
影响因子
1.6
CiteScore
3.1
期刊收录
SCI、SCIE

Molecular Genetics & Genomic Medicine(中文译名:《分子遗传学和基因组医学》),ISSN:2324-9269,EISSN:2324-9269,是John Wiley and Sons Inc.出版的国际性学术期刊,创刊于2013年,以6 issues/year形式稳定发行,2026年总发文量约122篇。该刊采用OA开放访问,学科归属为Biochemistry, Genetics and Molecular Biology - Genetics。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1.6,2025年期刊CiteScore为3.1,2025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4区,在所属学科领域具备高学术影响力与国际认可度。Molecular Genetics & Genomic Medicine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14 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,CHINA MAINLANDUSA、Italy、GERMANY (FED REP GER)、Canada、Japan、Iran等为核心发文国家与地区;SHANGHAI JIAO TONG UNIVERSITYCHINESE ACADEMY OF MEDICAL SCIENCES - PEKING UNION MEDICAL COLLEGE、CENTRAL SOUTH UNIVERSITY、BAYLOR COLLEGE OF MEDICINE、UNIVERSITY OF CALIFORNIA SYSTEM、HARVARD UNIVERSITY、CAPITAL MEDICAL 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
医学
4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
医学
4区
GENETICS & HEREDITY 遗传学
4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
4区
GENETICS & HEREDITY 遗传学
4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 Q4 151 / 192

21.6

学科:GENETICS & HEREDITY SCIE Q4 153 / 192

20.57

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 Q4 147 / 191

23.3

学科:GENETICS & HEREDITY SCIE Q3 142 / 191

25.92


中国学者近期发文

1
A Genetic Landscape of Euploid Miscarriages From Couples With Recurrent Pregnancy Loss Through Whole Exome Sequencin

Author:Kong, Fanjuan; Yin, Zhaochu; Zhou, Haiyan; Liu, Zhiyu; Xie, Wanqin

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 4, pp. -. DOI: 10.1002/mgg3.70220

2
Prenatal Diagnosis of Autosomal Recessive Primary Microcephaly Type 2 Caused by Compound Heterozygous WDR62 Variants in a Family With Two Recurrent Case

Author:Li, Yan-Fang; Zhang, Song-Hui; Zhen, Li; Zhang, Lan-Zhen

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 4, pp. -. DOI: 10.1002/mgg3.70203

3
Association Between Cerebellar Metabolic Markers and Activities of Daily Living in Patients With Spinocerebellar Ataxia Type

Author:Ye, Mei; Qiu, Xiao Ping; Zhang, Shengnan; Wang, Ling; Gao, Zhongming; Liu, Mengyu; Feng, Yaping

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 4, pp. -. DOI: 10.1002/mgg3.70197

4
Novel Compound Heterozygous Variants in the COG5 Gene Causing Fetal Hydrops and Skeletal Dysplasi

Author:Yang, Qi; He, Wei; Zhang, Qiang; Yi, Sheng; Zhou, Xunzhao; Wang, Linlin; Yi, Shang; Qin, Zailong; Luo, Jingsi

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 4, pp. -. DOI: 10.1002/mgg3.70215

5
Analysis of the Phenotype and Gene Mutations of Two Families With Combined Mutations of Anticoagulant Protein Gene

Author:Guo, Yueli; Shan, Tingting; Zheng, Wenjieying; Zhao, Chun; Kong, Wanzhong; Zou, Xiaojing

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 4, pp. -. DOI: 10.1002/mgg3.70191

6
Clinical Utility of Prenatal cfDNA Screening for Sex Chromosome Aneuploidies: A Single Center Experienc

Author:Lin, Ying; Lu, Qun; Wu, Yun; Li, Hang; Feng, Haoyang; Luo, Chunyu; Hu, Ping; Liang, Dong; Xu, Zhengfeng

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 3, pp. -. DOI: 10.1002/mgg3.70211

7
Identification of a Homozygous PGM2L1 Variant in a Male Patient With Developmental Delay and Seizure

Author:Niu, Mengmeng; Wang, Dong; Jia, Shanshan

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 3, pp. -. DOI: 10.1002/mgg3.70195

8
Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Childre

Author:Li, Yuzhuopu; Wang, Yang; Liu, Tao; Xiao, Li; Huang, Lan; Zhang, Yongjie; Xiang, Yan; Yu, Jie

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 3, pp. -. DOI: 10.1002/mgg3.70188

9
Pathogenic Variants and Olipudase Alfa Treatment of Patients With Acid Sphingomyelinase Deficiency in Taiwa

Author:Lin, Hsu-Heng; Chen, Hui-An; Lin, Shyh-Jer; Hsu, Rai-Hseng; Lee, Ni-Chung; Hwu, Wuh-Liang; Ni, Yen-Hsuan; Chou, Yen-Yin; Chiu, Pao-Chin; Peng, Steven Shinn-Forng; Chien, Yin-Hsiu

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 2, pp. -. DOI: 10.1002/mgg3.70204

10
A Novel A-Kinase-Anchoring Protein 9 Variant in Premature Coronary Artery Disease: A Case Serie

Author:Jiao, Yuemiao; Wang, Minxian; Qiang, Guifen; Zhao, Li; Xi, Ziwei; Yu, Yue; Yin, Chengqian; Song, Guangyuan

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2026; Vol. 14, Issue 1, pp. -. DOI: 10.1002/mgg3.70159


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Molecular Genetics & Genomic Medicine

国际简称:MOL GENET GENOM MED参考译名:分子遗传学和基因组医学

年发文量:122 CiteScore:3.1 是否预警:否 Gold OA文章占比:99.80% 研究类文章占比:95.90%

杂志社联系方式:111 RIVER ST, HOBOKEN, USA, NJ, 07030-5774

Molecular Genetics & Genomic Medicine