Molecular Genetics & Genomic Medicine SCIE

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

主要研究方向：Biochemistry, Genetics and Molecular Biology-Genetics 非预警期刊审稿周期： 14 Weeks

《分子遗传学和基因组医学》(Molecular Genetics & Genomic Medicine)是一本由John Wiley and Sons Inc.出版的以Biochemistry, Genetics and Molecular Biology-Genetics为研究特色的国际期刊，发表该领域相关的原创研究文章、评论文章和综述文章，及时报道该领域相关理论、实践和应用学科的最新发现，旨在促进该学科领域科学信息的快速交流。该期刊是一本开放期刊，近三年没有被列入预警名单。

4区中科院分区
Q4 JCR分区
196 年发文量
1.5 IF影响因子
开放是否OA
2 H-index
2013 创刊年份
6 issues/year 出版周期
English 出版语言

Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care.

Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.

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Molecular Genetics & Genomic Medicine期刊信息

ISSN：2324-9269
出版语言：English
是否OA：开放
E-ISSN：2324-9269
出版地区：United States
是否预警：否
出版商：John Wiley and Sons Inc.
出版周期：6 issues/year
创刊时间：2013
开源占比：0.7303
Gold OA文章占比：68.56%
OA被引用占比：1
出版国人文章占比：0.32
出版撤稿占比：0
研究类文章占比：87.24%

Molecular Genetics & Genomic Medicine CiteScore评价数据（2024年最新版）

CiteScore

SJR

SNIP

CiteScore 指数

4.2

0.633

0.696

学科类别	分区	排名	百分位
大类：Medicine 小类：Genetics (clinical)	Q3	55 / 99	44%
大类：Medicine 小类：Genetics	Q3	203 / 347	41%
大类：Medicine 小类：Molecular Biology	Q3	284 / 410	30%

名词解释：CiteScore 是衡量期刊所发表文献的平均受引用次数，是在 Scopus 中衡量期刊影响力的另一个指标。当年CiteScore 的计算依据是期刊最近4年（含计算年度）的被引次数除以该期刊近四年发表的文献数。例如，2022年的 CiteScore 计算方法为：2022年的 CiteScore =2019-2022年收到的对2019-2022年发表的文件的引用数量÷2019-2022年发布的文献数量注：文献类型包括：文章、评论、会议论文、书籍章节和数据论文。

Molecular Genetics & Genomic Medicine中科院评价数据

中科院 2023年12月升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	医学	4区	GENETICS & HEREDITY 遗传学	4区

中科院 2022年12月升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	医学	4区	GENETICS & HEREDITY 遗传学	4区

中科院 2021年12月旧的升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	医学	4区	GENETICS & HEREDITY 遗传学	4区

中科院 2021年12月基础版

Top期刊	综述期刊	大类学科		小类学科
否	否	医学	4区	GENETICS & HEREDITY 遗传学	4区

中科院 2021年12月升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	医学	4区	GENETICS & HEREDITY 遗传学	4区

中科院 2020年12月旧的升级版

Top期刊	综述期刊	大类学科		小类学科
否	否	医学	4区	GENETICS & HEREDITY 遗传学	4区

Molecular Genetics & Genomic Medicine JCR评价数据（2023-2024年最新版）

按JIF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%

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	142 / 191	25.92%

Molecular Genetics & Genomic Medicine历年数据统计

影响因子

中科院分区

Molecular Genetics & Genomic Medicine中国学者发文选摘

1、The effect of growth hormone treatment in children with novel BPTF gene variants: A report of two cases and literature review
Author: Wu, Wenyong; Chen, Ruimin

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2066
2、A novel splicing variant of VCAN identified in a Chinese family initially diagnosed with familial exudative vitreoretinopathy
Author: Zhong, Junwei; Shi, Jie; Zhang, Xiaotian; Xu, Ke; Zhang, Xiaohui; Xie, Yue; Li, Yang

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 2, pp. -. DOI: 10.1002/mgg3.2083
3、Association of demographic and clinical factors with risk of acute pancreatitis: An exposure-wide Mendelian randomization study
Author: Tang, Qiu-Yi; Yang, Qi; Yu, Xian-Qiang; Liu, Yu-Xiu; Tong, Zhi-Hui; Li, Bai-Qiang; Chen, Ya-Ting; Yu, Evan Yi-Wen; Li, Wei-Qin

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2091
4、Compound heterozygous loss-of-function variants in BRAT1 cause lethal neonatal rigidity and multifocal seizure syndrome
Author: Li, Shan; Yu, Shunan; Zhang, Yanzhuo; Wang, Ying; Jiang, Xu; Wu, Chengai

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2092
5、Nance-Horan syndrome pedigree due to a novel microdeletion and skewed X chromosome inactivation
Author: Huang, Yazhou; Ma, Linya; Zhang, Zhaoxia; Nie, Shujuan; Zhou, Yuan; Zhang, Jibo; Wang, Chao; Fang, Xingxin; Quan, Yingting; He, Ting; Liu, Anhui; Peng, Dan

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 2, pp. -. DOI: 10.1002/mgg3.2100
6、The compound heterozygous mutations of c.607G > a and c.657delC in the FAH gene are associated with renal damage with hereditary tyrosinemia type 1 (HT1)
Author: Chi, Huan; Gan, Chun; Jiang, Yaru; Chen, Dan; Qiu, Jiawen; Yang, Qing; Chen, Yaxi; Wang, Mo; Yang, Haiping; Jiang, Wei; Li, Qiu

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2090
7、A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4
Author: Yang, Kun; Wang, Xi; Wang, Wei-Qian; Han, Ming-Yu; Hu, Li-Min; Kang, Dong-Yang; Yang, Jin-Yuan; Liu, Min; Gao, Xue; Yuan, Yong-Yi; Xu, Jin-Cao

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 3, pp. -. DOI: 10.1002/mgg3.2103
8、BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity
Author: Yang, Shangying; Li, Zhen; Cheng, Wanyu; Ma, Meijiao; Qi, Rui; Rui, Xue; Ren, Yinghua; Sheng, Xunlun; Rong, Weining

Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2095