Rare Disease and Orphan Drugs Journal
About the journal
The Rare Disease and Orphan Drugs Journal (RDODJ) is an international, peer-reviewed, open-access journal dedicated to advancing research on the genetic and molecular basis of rare diseases and promoting translational research in their diagnosis, prevention, and treatment. RDODJ provides a forum for scientific research and scholarly discussion on key regulatory, socioeconomic, and humanistic issues related to rare diseases and orphan drugs.
10 Jul 2024
Investigating Fabry disease - some lessons learned
22 Jan 2024
Gene therapy for Dravet syndrome: promises and impact on disease trigger and secondary modifications
8 Jul 2024
Managing pregnancy in women with sickle cell disease: a focus on physiopathology, risks, and multidisciplinary care
24 Jun 2025
Gene therapy for inborn errors of immunity: past progress, current status and future directions
17 Oct 2025
The dynamic and urgent path of rare disease and orphan drug research
15 Mar 2021
Topics Collection
Topic: Advancements in Diagnosis and Treatment of Familial Hypercholesterolemia Submission deadline: 31 Mar 2025
Topic: Duchenne Muscular Dystrophy (DMD): Progress in Research and Insights Submission deadline: 31 Mar 2025
Topic: Advances in Neurofibromatosis - The Future is Bright Submission deadline: 28 Feb 2025695
Authors
1008
Reviewers
2021
Published Since
Rare Disease and Orphan Drugs Journal
Editor-in-Chief: Daniel Scherman
Indexing: ESCI, Scopus, Dimensions, Lens, ASCI
Median time to first editorial decision: 7 days
1.9 Impact Factor
2.1 CiteScore
1.9 Impact Factor
2.1 CiteScore
The European joint programme on rare diseases: building the rare diseases resear...
23 Jun 2024
The complexity of funding rare disease research: an IRDiRC assessment of the lan...
8 Sep 2024
Investigating Fabry disease - some lessons learned
22 Jan 2024
The inflammatory pathogenetic pathways of Fabry nephropathy
17 Apr 2024
Topic: Precision Nutrition and Personalized Therapeutic Strategies for Rare Metabolic Diseases
Submission Deadline: 30 Jun 2027 Published articles: 0
Topic: Latest Advances in Rare Neurological Disorders
Submission Deadline: 28 Feb 2027 Published articles: 0
Topic: Advancements in Diagnosis and Treatment of Familial Hypercholesterolemia Submission deadline: 31 Mar 2025
Topic: Duchenne Muscular Dystrophy (DMD): Progress in Research and Insights Submission deadline: 31 Mar 2025
Topic: Advances in Neurofibromatosis - The Future is Bright Submission deadline: 28 Feb 2025
Academic Talks
Interview with Prof. Janet Woodcock: From Regulatory Leadership to Rare Disease Innovation
695
Authors
1008
Reviewers
2021
Published Since



































(1)-20220628.png)






-20221212.png)






















-20221026.png)
-20221026.png)

















