当前位置: X-MOL首页SCI期刊查询及投稿分析系统 › Orphanet Journal of Rare Diseases杂志
Orphanet Journal of Rare Diseases
基本信息
期刊名称 Orphanet Journal of Rare Diseases
ORPHANET J RARE DIS
期刊ISSN 1750-1172
期刊官方网站 https://ojrd.biomedcentral.com
是否OA Yes
出版商 BioMed Central Ltd
出版周期 Irregular
文章处理费 登录后查看
始发年份 2006
年文章数 357
影响因子 3.4(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2区 GENETICS & HEREDITY 遗传学3区
MEDICINE, RESEARCH & EXPERIMENTAL 医学:研究与实验3区
CiteScore
CiteScore排名 CiteScore SJR SNIP
学科 排名 百分位 6.3 1.182 1.464
Medicine
Pharmacology (medical)
67/272 75%
Medicine
Genetics (clinical)
33/99 67%
补充信息
自引率 5.9%
H-index 87
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=1750-1172%5BISSN%5D
投稿指南
期刊投稿网址 https://www.editorialmanager.com/ojrd
收稿范围
Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports which do not present clinical or pathological findings that can provide information about the mechanisms of a disease. Case reports which just present phenotype information, should not be considered.
收录体裁
Research
Review
Letter to the Editor
Position statement
投稿指南 https://ojrd.biomedcentral.com/submission-guidelines
投稿模板 https://ojrd.biomedcentral.com/submission-guidelines/preparing-your-manuscript
参考文献格式 https://ojrd.biomedcentral.com/submission-guidelines/preparing-your-manuscript
编辑信息

Editor-in-Chief
Francesc Palau, Hospital Sant Joan de Déu Barcelona and CIBERER, Spain 

Managing Editor
Virginia Corrochano, Centre for Biomedical Network Research on Rare Diseases, Spain

Section Editors

Clinical genetics and genomics
Nan Wu, Baylor College of Medicine, USA

Dysmorphology
Miguel del Campo, University of California- San Diego, USA

Inherited metabolic diseases
Manuela de Almeida Roediger, Universidade de São Paulo, Brazil
Kimberly Chapman, Children's National Health System, USA
Jeff Guo, University of Cincinnati, USA
Iain Hargreaves, Liverpool John Moores University and National Hospital, UK
Hilary Vernon, Johns Hopkins University, USA

Lysosomal storage diseases
Walla Al-Hertani, Boston Children’s Hospital, USA
Manisha Balwani, Icahn School of Medicine at Mount Sinai, USA
Bruno Bembi, University Hospital of Udine, Italy 
Jaya Ganesh, Icahn School of Medicine at Mount Sinai, USA 
Manoj Pandey, Cincinnati Children's Hospital, USA
Gregory Pastores, National Center for Inherited Metabolic Diseases, Ireland 
Raymond Wang, CHOC Children’s, USA

Mitochondrial Diseases
Rafael Artuch, Hospital Sant Joan de Déu, Spain
Daniele Ghezzi, Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta, Italy 

Orphan drugs/ Health economics
Benoit Arnould, ICON, France
Mikel Berdud, The Office of Heath Economics, UK
Nuria Carrillo, National Human Genome Research Institute, USA
Dyfrig Hughes, Bangor University, UK
Rosa Rodriguez-Monguio, University of California, San Francisco, USA

Pediatric neuromuscular diseases
Janbernd Kirschner, University Medical Center Freiburg, Germany
Carmen Paradas López, Hospital Universitario Virgen del Rocio, Spain

Pediatric oncology
Karlyne M Reilly, National Cancer Institute, USA

Pediatric rheumatological diseases
Frank Dressler, Medizinische Hochschule, Germany

Rare bone diseases and skeletal dysplasias 
Christina Lampe, University of Gießen, Germany
Klaus Mohnike, Otto-von-Guericke Universität, Germany
Nan Wu, Baylor College of Medicine, USA

Rare cardiovascular diseases
Roberto Barriales-Villa, Complexo Hospitalario Universitario A Coruña, Spain
Ken-ichi Hirano, Osaka University, Japan

Rare coagulation diseases
Flora Peyvandi, University of Milan, Italy

Rare endocrinological diseases
Maria Luisa Brandi, Università degli Studi di Firenze, Italy
Bruno Donadille, Hôpital Saint Antoine, France
Xiaomu Kong, China-Japan Friendship Hospital, China

Rare gastrointestinal diseases
Jorge Amil Dias, Hospital São João, Portugal 
Sumantra Chatterjee, NYU Langone Health, USA

Rare immune deficiencies
Andrew Gennery, Newcastle University, UK

Rare kidney diseases
Olivier Devuyst, University of Zurich, Switzerland

Rare neurological diseases
Marc Engelen, Amsterdam Universitair Medische Centra, The Netherlands
Anna Lehman, University of British Columbia, Canada
Elizabeth McNeil, NIH, USA
Yi-Cheng Zhu, Peking Union Medical College Hospital, China

Rare opthalmological diseases
Isabelle Audo, INSERM, France

Rare pulmonary diseases
Kai-Feng Xu, Peking Union Medical College Hospital, China

Rare skin diseases
Cristina Has, Universitätsklinikum Freiburg, Germany
Giovanna Zambruno, Istituto Dermopatico dell'Immacolata, Italy

Registries/ Health planning/ Health services
Tatiana Foltánová, Comenius University in Bratislava, Slovakia
Lidia García-Pérez, SESCS, Spain

Editorial Board
Fowzan Alkuraya, KFSHRC, Saudi Arabia 
Robert Anderson, University College London, UK 
Marieke Biegstraaten, Academic Medical Center, Netherlands 
Jean-Yves Blay, Université Claude Bernard Lyon I, France
Francesc Cardellach, University of Barcelona School of Medicine, Spain
Vincent Cottin, Hopital L Pradel, France 
Matthias Griese, Ludwig-Maximilians University of Munich, Germany 
Helena Kääriäinen, National Institute for Health and Welfare, Finland
Jennifer Kalish, University of Pennsylvania, USA 
Lisa Licitra, Istituto Nazionale Tumori, Italy
Milan Macek, Charles University and Motol University Hospital, Czech Republic
Ute Moog, University of Heidelberg, Germany 
Massimo Pandolfo, Université Libre de Bruxelles, Belgium 
Anne Slavotinek, UCSF, United States of America 
Ronald Sokol, University of Colorado School of Medicine, USA
Constantinos Stratakis, NICHD, NIH, USA 
Antonella Tosti, University of Miami Miller School of Medicine, USA 
Juan Tovar, University Hospital La Paz, Spain 
Alain Verloes, Hôpital Robert DEBRE, France 
Andrea Vincent, University of Auckland, New Zealand 
Joan-Lluis Vives Corrons, University of Barcelona, Spain
Dagmar Wieczorek, Universitätsklinikum Essen, Germany 
Frits Wijburg, Academic Medical Center, Netherlands
Christina Zeitz, Université Pierre et Marie Curie, INSERM, France


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