Molecular Genetics & Genomic Medicine SCIE

國際簡稱：MOL GENET GENOM MED 參考譯名：分子遺傳學和基因組醫(yī)學

主要研究方向：Biochemistry, Genetics and Molecular Biology-Genetics 非預警期刊審稿周期： 14 Weeks

《分子遺傳學和基因組醫(yī)學》(Molecular Genetics & Genomic Medicine)是一本由John Wiley and Sons Inc.出版的以Biochemistry, Genetics and Molecular Biology-Genetics為研究特色的國際期刊，發(fā)表該領(lǐng)域相關(guān)的原創(chuàng)研究文章、評論文章和綜述文章，及時報道該領(lǐng)域相關(guān)理論、實踐和應(yīng)用學科的最新發(fā)現(xiàn)，旨在促進該學科領(lǐng)域科學信息的快速交流。該期刊是一本開放期刊，近三年沒有被列入預警名單。

4區(qū) 中科院分區(qū)
Q4 JCR分區(qū)
196 年發(fā)文量
1.5 IF影響因子
開放是否OA
2 H-index
2013 創(chuàng)刊年份
6 issues/year 出版周期
English 出版語言

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
出版語言：English
是否OA：開放
E-ISSN：2324-9269
出版地區(qū)：United States
是否預警：否
出版商：John Wiley and Sons Inc.
出版周期：6 issues/year
創(chuàng)刊時間：2013
開源占比：0.7303
Gold OA文章占比：68.56%
OA被引用占比：1
出版國人文章占比：0.32
出版撤稿占比：0
研究類文章占比：87.24%

Molecular Genetics & Genomic Medicine CiteScore評價數(shù)據(jù)（2024年最新版）

CiteScore

SJR

SNIP

CiteScore 指數(shù)

4.2

0.633

0.696

學科類別	分區(qū)	排名	百分位
大類：Medicine 小類：Genetics (clinical)	Q3	55 / 99	44%
大類：Medicine 小類：Genetics	Q3	203 / 347	41%
大類：Medicine 小類：Molecular Biology	Q3	284 / 410	30%

名詞解釋：CiteScore 是衡量期刊所發(fā)表文獻的平均受引用次數(shù)，是在 Scopus 中衡量期刊影響力的另一個指標。當年CiteScore 的計算依據(jù)是期刊最近4年（含計算年度）的被引次數(shù)除以該期刊近四年發(fā)表的文獻數(shù)。例如，2022年的 CiteScore 計算方法為：2022年的 CiteScore =2019-2022年收到的對2019-2022年發(fā)表的文件的引用數(shù)量÷2019-2022年發(fā)布的文獻數(shù)量注：文獻類型包括：文章、評論、會議論文、書籍章節(jié)和數(shù)據(jù)論文。

Molecular Genetics & Genomic Medicine中科院評價數(shù)據(jù)

中科院 2023年12月升級版

Top期刊	綜述期刊	大類學科		小類學科
否	否	醫(yī)學	4區(qū)	GENETICS & HEREDITY 遺傳學	4區(qū)

中科院 2022年12月升級版

Top期刊	綜述期刊	大類學科		小類學科
否	否	醫(yī)學	4區(qū)	GENETICS & HEREDITY 遺傳學	4區(qū)

中科院 2021年12月舊的升級版

Top期刊	綜述期刊	大類學科		小類學科
否	否	醫(yī)學	4區(qū)	GENETICS & HEREDITY 遺傳學	4區(qū)

中科院 2021年12月基礎(chǔ)版

Top期刊	綜述期刊	大類學科		小類學科
否	否	醫(yī)學	4區(qū)	GENETICS & HEREDITY 遺傳學	4區(qū)

中科院 2021年12月升級版

Top期刊	綜述期刊	大類學科		小類學科
否	否	醫(yī)學	4區(qū)	GENETICS & HEREDITY 遺傳學	4區(qū)

中科院 2020年12月舊的升級版

Top期刊	綜述期刊	大類學科		小類學科
否	否	醫(yī)學	4區(qū)	GENETICS & HEREDITY 遺傳學	4區(qū)

Molecular Genetics & Genomic Medicine JCR評價數(shù)據(jù)（2023-2024年最新版）

按JIF指標學科分區(qū)	收錄子集	分區(qū)	排名	百分位
學科：GENETICS & HEREDITY	SCIE	Q4	147 / 191	23.3%

按JCI指標學科分區(qū)	收錄子集	分區(qū)	排名	百分位
學科：GENETICS & HEREDITY	SCIE	Q3	142 / 191	25.92%

Molecular Genetics & Genomic Medicine歷年數(shù)據(jù)統(tǒng)計

影響因子

中科院分區(qū)

Molecular Genetics & Genomic Medicine中國學者發(fā)文選摘

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