首页 国际期刊 医学期刊 期刊详情(非官网)
400-808-1701

Journal Of Medical Genetics

Journal Of Medical Genetics杂志,由BMJ Publishing Group出版,于1964年创刊,Monthly,出版语言English,ISSN:0022-2593,E-ISSN:1468-6244。

投稿咨询
Journal Of Medical Genetics
Journal Of Medical Genetics
Journal Of Medical 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
8.2
期刊收录
SCI、SCIE

Journal Of Medical Genetics(中文译名:《医学遗传学杂志》),ISSN:0022-2593,EISSN:1468-6244,是BMJ Publishing Group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112篇。该刊采用非OA开放访问,学科归属为医学 - 遗传学。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3.4,2025年期刊CiteScore为8.2,2025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。Journal Of Medical Genetics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,USAEngland、CHINA MAINLAND、Netherlands、France、GERMANY (FED REP GER)、Canada等为核心发文国家与地区;INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)ASSISTANCE PUBLIQUE HOPITAUX PARIS (APHP)、UNIVERSITY OF LONDON、UNIVERSITE DE PARIS、UNIVERSITY OF CAMBRIDGE、LEIDEN UNIVERSITY、UNIVERSITY OF MANCHESTER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
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 Q1 48 / 192

75.26

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 52 / 192

73.2

学科:GENETICS & HEREDITY SCIE Q1 45 / 192

76.82


中国学者近期发文

1
Expanded carrier screening in a Southwestern Chinese population indicates East Asian specific low-frequency pathogenic variants account for nearly half of the at-risk couple rat

Author:Liu, Sha; Cao, Liyuan; Zhang, Victor Wei; Huang, Shuang; Liu, Haipeng; Wei, Xiang; Luo, Yuan; Li, Yue; Zhou, Lin; Jiang, Linzhi; Zhu, Qian; Liu, Hongqian

Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111273

2
Clinical characteristics and prognosis of SDHD pathogenic variant carriers: a systematic review and meta-analysi

Author:Lian, Xinquan; Shen, Liping; Song, Jiayin; Pang, Mengqi; Zhong, Yunmeng; Zhang, Han; Xing, Yadong; Tung, Tao-Hsin; Shen, Bo

Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111235

3
Evaluating the efficiency of nanopore adaptive sampling sequencing in detecting balanced translocatio

Author:Gao, Meng; Ren, Jun; Peng, Cuiting; Liu, Xijing; Zheng, Jiemei; Chen, Han; Chen, Xinlian; Wang, Jiamin; Lai, Yi; Hu, Ting; Liu, Shanling

Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111347

4
Comparison of clinical characteristics between patients with single mutation and co-mutation in hereditary renal cancer: a retrospective analysis of 115 patients with von Hippel-Lindau syndrom

Author:Liu, Tao; Liu, Haode; Deng, Ruiyi; Jianhui, Qiu; Zhang, Zedan; Wang, Chuandong; Bao, Yuhang; Chen, Xiaolin; Song, Zheng; He, Tianyi; Cai, Lin; Wang, Yizhou; Zhou, Jingcheng; Gong, Kan

Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111303

5
Comprehensive genotype-phenotype correlation analysis in 11 509 neonates carrying common deafness-associated pathogenic variant

Author:Li, Jianjun; Zhan, Zijun; Zhang, Xiao; Wu, Bo; Liu, Wenlan

Journal: JOURNAL OF MEDICAL GENETICS. 2026; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-111135

6
Whole-exome sequencing reveals sex difference in the genetic architecture of high myopi

Author:Liu, Xingchen; Liang, Jiacheng; Li, Shasha; Yang, Yuhe; Zhu, Qinghao; Qiu, Ruowen; Chen, Zheng Ji; Yao, Yinghao; Ren, Qing; Yu, Xiaoguang; Qu, Jia; Su, Jianzhong; Yuan, Jian

Journal: JOURNAL OF MEDICAL GENETICS. 2025; Vol. 62, Issue 5, pp. 358-368. DOI: 10.1136/jmg-2024-110467

7
A novel 8-octapeptide repeat insertion in PRNP causing Huntington disease-like 1 in a Chinese family: a case report and literature revie

Author:Ni, Jie; Zheng, Fangxue; Yu, Lihua; He, Fangping; Ji, Fang; Ling, Yi; Liu, Ping; Peng, Guoping; Ke, Qing

Journal: JOURNAL OF MEDICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2024-110520

8
The γ-Actin with pathogenic variants of sites on actin-binding proteins caused earlier onset and more malignant progressive hearing los

Author:Li, Sijun; Feng, Qi; Mei, Lingyun; Zhang, Shuai; Song, Jian; Feng, Yong; Wu, Xuewen

Journal: JOURNAL OF MEDICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2024-110573

9
Identification of MACF1 as a causative gene of generalised epileps

Author:Lei, Xiao-Yun; Zhang, Meng-Wen; Sun, Hui; Song, Wang; Liang, Xiao-Yu; Wang, Cui-Shan; Luo, Sheng; Li, Bing-Mei; Liu, Xiao-Rong; Wang, Yao; Tian, Yang; Peng, Qian; Wang, Jie; Meng, Heng; He, Na; Liao, Wei-Ping

Journal: JOURNAL OF MEDICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2025-110699

10
Clinical and genetic characteristics of PLA2G6-related parkinsonism in Southwest China and a comprehensive literature revie

Author:Cheng, Yangfan; Zhang, Yang; Xiao, Yi; Wang, Shichan; Chen, Sihui; Zheng, Xiaoting; Yang, Tianmi; Jiang, Qirui; Huang, Jingxuan; Lin, Junyu; Ou, Ruwei; Li, Chunyu; Wei, Qianqian; Chen, Xueping; Shang, Huifang

Journal: JOURNAL OF MEDICAL GENETICS. 2025; Vol. , Issue , pp. -. DOI: 10.1136/jmg-2024-110479


在线咨询

Journal Of Medical Genetics

国际简称:J MED GENET参考译名:医学遗传学杂志

年发文量:112 CiteScore:8.2 是否预警:否 Gold OA文章占比:32.76% 研究类文章占比:96.43%

杂志社联系方式:B M J PUBLISHING GROUP, BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON, ENGLAND, WC1H 9JR

Journal Of Medical Genetics