当前位置: X-MOL首页SCI期刊查询及投稿分析系统 › Molecular Genetics & Genomic Medicine杂志
Molecular Genetics & Genomic Medicine
基本信息
期刊名称 Molecular Genetics & Genomic Medicine
MOL GENET GENOM MED
期刊ISSN 2324-9269
期刊官方网站 https://onlinelibrary.wiley.com/journal/23249269
是否OA Yes
出版商 John Wiley & Sons Inc.
出版周期
文章处理费 登录后查看
始发年份
年文章数 196
影响因子 1.5(2023)  scijournal影响因子  greensci影响因子
中科院SCI期刊分区
大类学科 小类学科 Top 综述
医学3区 GENETICS & HEREDITY 遗传学4区
CiteScore
CiteScore排名 CiteScore SJR SNIP
学科 排名 百分位 4.2 0.633 0.696
Medicine
Genetics (clinical)
55/99 44%
Biochemistry, Genetics and Molecular Biology
Genetics
203/347 41%
Biochemistry, Genetics and Molecular Biology
Molecular Biology
284/410 30%
补充信息
自引率 6.7%
H-index 2
SCI收录状况 Science Citation Index Expanded
官方审稿时间 登录后查看
网友分享审稿时间 数据统计中,敬请期待。
接受率 登录后查看
PubMed Central (PMC) http://www.ncbi.nlm.nih.gov/nlmcatalog?term=2324-9269%5BISSN%5D
投稿指南
期刊投稿网址 https://mc.manuscriptcentral.com/MGGM
收稿范围
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. Simple, purely descriptive, single-patient Case Reports are out of scope for this journal. For such Case Reports we recommend considering submission to Case Reports in Genetics.
收录体裁
投稿指南 https://onlinelibrary.wiley.com/page/journal/23249269/homepage/forauthors.html
投稿模板
参考文献格式
编辑信息

EDITOR-IN-CHIEF

(USA)Suzanne Hart* (National Human Genome Research Institute, NIH, Bethesda, Maryland, USA; Email: MGGM@wiley.com)


*Dr. Hart serves in her own capacity





ASSOCIATE EDITORS

(USA)Paul Kruszka* (National Human Genome Research Institute, NIH, Bethesda, Maryland, USA)


(Hong Kong)Wanling Yang (University of Hong Kong, Hong Kong SAR, P.R. China)


(USA)Yingze Zhang (University of Pittsburgh, Pennsylvania, USA)


*Dr. Kruszka serves in his own capacity





FOUNDING EDITOR

(USA)Maximilian Muenke* (National Human Genome Research Institute, NIH, Bethesda, Maryland, USA)


*Dr. Muenke serves in his own capacity





EDITORIAL BOARD

(Sweden)Eleni Aklillu (Karolinska Institutet, Sweden)


(Saudi Arabia)Fowzan S. Alkuraya (College of Medicine, Alfaisal University, Saudi Arabia)


(Israel)Yair Anikster (Sheba Medical Center, Israel)


(Colombia)Mauricio Arcos-Burgos (Universidad del Rosario, Colombia)


(Turkey)Nurten A. Akarsu (Hacetepe University, Turkey)


(USA)Michael Bamshad (University of Washington School of Medicine, USA)


(Canada)Kym Boycott (Children's Hospital of Eastern Ontario and University of Ottawa, Canada)


(Chile)María Leonor Bustamente Calderón (University of Chile, Chile)


(Canada)Ronald D. Cohn (University of Toronto, Canada)


(France)Véronique David (University of Rennes, France)


(USA)Mauricio De Castro (Air Force Medical Genetics Center, USA)


(USA)Michael J. Gambello (Emory University, USA)


(USA)Andrea Gropman (Children's National Medical Center, USA)


(USA)Ophir Klein (University of California, San Francisco, USA)


(UK)Robert Kleta (University College London, United Kingdom)


(Czech Republic)Stanislav Kmoch (Charles University in Prague, Czech Republic)


(Brazil)Maria Rita Passos-Bueno (University of Sao Paulo, Brazil)


(India)Shubha R. Phadke (Sanjay Gandhi Postgraduate Institute of Medical Sciences, India)


(Singapore)Bruno Reversade (A*STAR, Singapore)


(USA)Lisa A. Schimmenti (Mayo Clinic, USA)


(Thailand)Vorasuk Shotelersuk (Chulalongkorn University, Thailand)


(USA)Anne Slavotinek (University of California, San Francisco, USA)


(The Netherlands)Joris Veltman (Radboud University Nijmegen Medical Centre, The Netherlands)


(Germany)Bernd Wollnik (Institute of Human Genetics Gottingen, Germany)


我要分享  (欢迎您来完善期刊的资料,分享您的实际投稿经验)
研究领域:
投稿录用情况: 审稿时间:  个月返回审稿结果
本次投稿点评:
提交
down
wechat
bug