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npj Genomic Medicine
基本信息
期刊名称 npj Genomic Medicine
NPJ GENOM MED
期刊ISSN 2056-7944
期刊官方网站 https://www.nature.com/npjgenmed/
是否OA
出版商 Nature Publishing Group
出版周期
始发年份
年文章数 32
最新影响因子 5.3(2022)  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
生物2区 GENETICS & HEREDITY 遗传学3区
CiteScore
CiteScore排名 CiteScore SJR SNIP
学科 排名 百分位 4.03 2.461 1.042
Medicine
Genetics(clinical)
18 / 91 80%
Biochemistry, Genetics and Molecular Biology
Genetics
59 / 318 81%
Biochemistry, Genetics and Molecular Biology
Molecular Biology
97 / 375 74%
补充信息
自引率 3.50%
H-index 11
SCI收录状况 Science Citation Index Expanded
官方审稿时间
网友分享审稿时间 数据统计中,敬请期待。
PubMed Central (PML) http://www.ncbi.nlm.nih.gov/nlmcatalog?term=2056-7944%5BISSN%5D
投稿指南
期刊投稿网址 https://mts-npjgenmed.nature.com/cgi-bin/main.plex?form_type=home
收稿范围

npj Genomic Medicine是一本国际经同行评审的期刊,致力于发行基因组及其在药学领域应用的论文,并具有重要的科学进展。该期刊将基因组医学定义为:使用通过基因组及其编码的分子而获知或支持的方法,对精神和身体疾病和紊乱进行诊断、预后、预防和治疗。 

期刊收录研究方向:综合表型和基因组数据及分析(包括免疫基因组学、药物基因组学、微生物组学和系统医学),疾病特异性多态性,与疾病和衰老相关的表观遗传学和表观基因组学,种系和新生突变(包括点突变,插入缺失和复制数变化),数据挖掘与人工智能,与疾病相关的3D基因组变异,新技术和信息学, 有关如何在患者的临床管理中使用这些数据的临床建议和指南,基因组药物患者效果的临床研究,学习与基因组医学有关的医疗保健系统,等

收录体裁
Article, Brief Communication, Case Report, Comment, Editorial, Matter Arising, Meeting Report, Perspective, Protocol, Review
投稿指南 https://www.nature.com/documents/npj-gta.pdf
投稿模板
参考文献格式 https://endnote.com/downloads/styles/
编辑信息

Editor-in-Chief

Stephen W. Scherer, PhD, DSc, FRSC
Director, The Centre for Applied Genomics
The Hospital for Sick Children and the University of Toronto McLaughlin Centre
Toronto, Canada 

Dr. Scherer holds the GlaxoSmithKline-Canadian Institutes of Health Research Endowed Chair in Genome Sciences at The Hospital for Sick Children (SickKids) and University of Toronto (UofT), and he is Director of the UofT McLaughlin Centre, as well as The Centre for Applied Genomics at SickKids. His research is documented in over 500 scholarly publications, and the Database of Genomic Variants he founded facilitates hundreds of thousands of clinical diagnoses each year. He has won numerous awards and Honorary Degrees, including the Steacie Prize, a Howard Hughes Medical Institute Scholarship and the Premier’s Summit Award for Medical Research. He is a Fellow of the Canadian Institute for Advanced Research, the American Association for the Advancement of Science and the Royal Society of Canada. In 2014, he was selected as a Thomson Reuters Citation Laureate in the field of Physiology or Medicine for “the discovery of large-scale copy number variation and its association with specific diseases.” 

Associate Editors

Mohammed Al-Qahtani, PhD
Executive Director, Center of Excellence in Genomic Medicine Research
King Abdulaziz University
Jeddah, Saudi Arabia

Prof. Mohammed Al-Qahtani is the Founder and Executive Director of the Center of Excellence in Genomic Medicine Research (CEGMR, since 2007) at King Abdulaziz University (KAU), Jeddah, Saudi Arabia. Prof. Al-Qahtani's research interest lies within the area of the development of molecular cytogenetic based diagnostics for cancer and other diseases. Prof. Al-Qahtani has more than 255 published manuscripts. In 2017, Prof. Al-Qahtani founded a central genetic lab (GenaTi) which offers a wide range of high-quality and cutting-edge genetic laboratory testing and internships. Prof. Al Qahtani is currently deputy vice president of King Abdulaziz University for Research Centers.

Charis Eng, MD, PhD
Hardis/ACS Professor and Chairwoman, Genomic Medicine Institute
Cleveland Clinic
OH, USA

Dr. Eng's laboratory seeks to identify and characterize genes that, when altered, predispose to cancer, using a range of strategies including clinical genetic, integrative omic, in vitro functional interrogation and non-human models. She also seeks to understand modifiers of heritable cancer risk including genomic, epigenomic and metagenomic modifiers. At the clinical interface, she is acknowledged as one of the rare “go to” people on what is and how to implement genetic- and genomics-enabled personalized healthcare.

Pui-Yan Kwok, MD, PhD
Institute of Biomedical Sciences Academia Sinica (Taiwan)
Cardiovascular Research Institute
University of California, San Francisco
CA, USA

Dr. Kwok's research focuses on developing tools and strategies to study the human genome and the role of human variation in common diseases. He developed single molecule strategies for genome mapping and rare genetic disease diagnosis. In addition, he recently launched an effort to bring genetics into clinical practice and implement precision management of common diseases. Dr. Kwok is an Academician of Academia Sinica and the recipient of the 2017 Distinguished Service Award from the University of Chicago Pritzker School of Medicine.

Dennis Lo, MD, PhD
Director, Li Ka Shing Institute of Health Sciences
The Chinese University of Hong Kong
Hong Kong, China


Dr. Lo is a key driver in the field of noninvasive prenatal testing. He discovered the presence of cell-free fetal DNA in maternal plasma, and his group has since remained at the forefront of this field. He has also pioneered a number of diagnostic applications of plasma DNA in other fields. He has received numerous awards, including the US National Academy of Clinical Biochemistry Distinguished Scientist Award (2006), a Croucher Senior Medical Research Fellowship, Sigi Zeiring Award from the American Association of Clinical Chemistry (2007) and Fulbright Distinguished Scholar (2009), among others. 

Stephen F. Kingsmore, MD, DSc
President and CEO
Rady Pediatric Genomics and Systems Medicine Institute
CA, USA
 

TIME magazine ranked Dr. Kingsmore and his team’s 2-day genome diagnosis method for NICU babies one of the top 10 medical breakthroughs of 2012. He was a MedScape Physician of the year in 2012, and received the 2013 Scripps Genomic Medicine award and 2013 ILCHUN prize of the Korean Society for Biochemistry and Molecular Biology. In 2016 and 2018, Dr. Kingsmore became the official title holder of the Guinness World Records® designation for fastest genetic diagnosis, which he accomplished by successfully diagnosing critically ill newborns in 26 and then 19 hours.

Lisa Strug, PhD
Assoc. Director, The Centre for Applied Genomics Senior Scientist
The Hospital for Sick Children
Toronto, Canada
 

In addition to her role at The Centre for Applied Genomics, she is also an Associate Prof.of Biostatistics and Statistical Sciences at the University of Toronto. Prof. Strug’s research interests lie in the fields of statistical genetics and genetic epidemiology. Her statistical work focuses on the development of pure likelihood methods for genetic analysis, methods for the analysis of next generation sequencing data and on methodology tailored to the identification of modifier genes for mendelian disorders. Her research investigates the genetic epidemiology of cystic fibrosis and the neurodevelopmental phenotype of common genetic epilepsies. Dr. Strug's team aims to translate genetic findings to identify therapeutic targets, and to build diagnostic and predictive models for early intervention.

Editorial Board

Dr. Muhammad Abu-Elmagd, PhD
Associate Professor, Center of Excellence in Genomic Medicine Research
King Abdulaziz University
Jeddah, Saudi Arabia

Dr. Stylianos E. Antonarakis, MD, PhD
Professor Emeritus of Genetic Medicine
University of Geneva Medical School
Geneva, Switzerland

Dr. Mourad Assidi, PhD
Assistant Professor, Center of Excellence in Genomic Medicine Research
King Abdulaziz University
Jeddah, Saudi Arabia

Dr. Thomas Bourgeron, PhD
Professor, University Paris Diderot
Head, Laboratory of Human Genetics and Cognitive Functions, Department of Neuroscience, Institut Pasteur
Paris, France

Prof. Adeel Chaudhary, PhD
Vice Director, Center of Excellence in Genomic Medicine Research
King Abdulaziz University
Jeddah, Saudi Arabia

Dr. Brian H.Y. Chung, MD, MSc
Associate Professor, Department of Paediatrics & Adolescent Medicine
LKS Faculty of Medicine
Hong Kong, China

Dr. Robert Davies, PhD
Associate Professor of Statistical and Population Genomics, Department of Statistics
University of Oxford
Oxford, United Kingdom

Prof. Emmanouil (Manolis) T. Dermitzakis, PhD
Professor, Department of Genetic Medicine and Development
University of Geneva Medical School
Geneva, Switzerland

Dr. Khalid A. Fakhro
Director, Human Genetics Department, Sidra Medicine
Assistant Professor of Genetic Medicine, Weill-Cornell Medical College
Ar-Rayyan, Qatar

Dr. Lars Feuk, PhD
Associate Professor, Department of Immunology, Genetics and Pathology (IGP)
Uppsala University
Uppsala, Sweden

Prof. Jozef Gecz, PhD
NH&MRC Principal Research Fellow and Chair for the Prevention of Childhood Disability
The University of Adelaide
North Adelaide, Australia

Dr. David Gurwitz, PhD
Director, NLGIP, Department of Human Molecular Genetics and Biochemistry Sackler Faculty of Medicine
Tel-Aviv University
Tel-Aviv, Israel

Prof. Jonathan Haines, PhD
Professor and Director, Institute of Computational Biology
Case Western Reserve University
Ohio, USA

Prof. Robert A. Hegele, MD, FRCPC, FACP
Director, Blackburn Cardiovascular Genetics Lab and London Regional Genomics Centre
Robarts Research Institute
Ontario, Canada

Prof. Taosheng Huang, MD, PhD
Director, Program of Mitochondrial Medicine; Director, Molecular Diagnostic laboratory
Division of Human Genetics, Cincinnati Children's Hospital Medical Center
Ohio, USA

Prof. Charles Lee, PhD
Scientific Director and Professor
The Jackson Laboratory for Genomic Medicine
Connecticut, USA

Prof. J. Steven Leeder, PharmD, PhD
Director, Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation
Children's Mercy Hospitals
Missouri, USA

Dr. Jeantine E. Lunshof, PhD
Assistant Professor, Department of Genetics
University of Groningen, University Medical Centre Groningen
Groningen, Netherlands

Dr. H. Tayfun Ozcelik, PhD
Dean, Department of Molecular Biology and Genetics
Bilkent University
Ankara, Turkey

Dr. Roger Pique-Regi, PhD
Assistant Professor, Center for Molecular Medicine and Genetics and Department of Obstetrics and Gynecology
Wayne State University
Michigan, USA

Prof. André Reis, M.D.
Director, Institute of Human Genetics
Friedrich-Alexander-Universität Erlangen-Nürnberg
Erlangen, Germany

Dr. Brent Richards, MD, MSc
Associate Professor, Departments of Medicine, Human Genetics, Epidemiology and Biostatistics
McGill University, Montreal
Québec, Canada

Wendy P. Robinson, PhD
Professor, Dept. of Medical Genetics
University of British Columbia
Senior Scientist, BC Children's Hospital Research Institute
Vancouver, Canada

Dr. Charles N. Rotimi, PhD
Director, Center for Research on Genomics and Global Health, NIH
Maryland, USA

Dr. Adam Shlien, PhD
Associate Director, Translational Genetics, Department of Paediatric Laboratory Medicine
The Hospital for Sick Children
Ontario, Canada

Dr. Kristiina Tammimies, PhD
Assistant Professor, Deputy Director of the Center for Neurodevelopmental Disorders, Department of Women's and Children's Health
Karolinska Institutet
Stockholm, Sweden

Prof. Joris Vermeesch, PhD
Department Chair, Head of Laboratory for Cytogenetics and Genome Research 
University of Leuven
Leuven, Belgium

Assistant Editor

Dr. Hin C. Lee, PhD
Program Manager, McLaughlin Centre
University of Toronto
Ontario, Canada

Nature Research

Managing Editor: Marie-Elizabeth Barabas, PhD
Editorial Assistant: Molly Jiang
Editorial Assistant Supervisor: Yasmin Esmaeili
Editorial Administration Manager: Colm Pollard
Publisher/Head of Outreach and Partnerships EMEA: Warren Raye, PhD
Director Strategic Partnerships Americas & Global NPJs: Andrea Macaluso
Production Editors:  David Pentney, Annika Jesse and Kate Neil
Assistant Production Editor: Amber Bhogal
Senior Production Editor: Jessica Hart
Publishing Assistant: Christine Hannon
Operations and Partnerships Manager: Esther Trinh
Senior Marketing Manager: Heather Dunphy
Head of Researcher Experience: Katherine Arundell
VP Editorial, Nature Research and Community Journals: Meredith LeMasurier, PhD
VP Commercial, Nature Research Group: Andrew Douglas
Chief Editorial Advisor, Nature Research: Magdalena Skipper, PhD

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