Orphanet Journal of Rare Diseases

SJR Rank #3,550H-index: 150SJR: 1.218Best quartile: Q1Open AccessAPC: US$2,990Listed in DOAJ

Journal website: aims, scope and author guidelines

Publisher

BioMed Central Ltd

Country

United Kingdom

Type

journal

SJR by Edition

Subject Categories

Medicine (miscellaneous)Q1
Pharmacology (medical)Q1
Genetics (clinical)Q2

Areas: Medicine

Most published research topics

Genomics and Rare DiseasesLysosomal Storage Disorders ResearchMetabolism and Genetic DisordersGlycogen Storage Diseases and MyoclonusHealth Systems, Economic Evaluations, Quality of LifeConnective tissue disorders researchNeurogenetic and Muscular Disorders ResearchMitochondrial Function and PathologyGenetic Neurodegenerative DiseasesAmyloidosis: Diagnosis, Treatment, Outcomes

Source: OpenAlex

Publication Statistics

Documents per Year

Detailed Information

ISSN

1750-1172

SJR Best Quartile

Region

Western Europe

Citations per Document (2 years)

3.51

References per Document

42.97

Coverage

2006-2026

Scope

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.

Metrics from SCImago Journal Rank 2025. View on SCImago