About the journal
Therapeutic Advances in Rare Disease is an open-access journal published by SAGE Publishing in United Kingdom, publishing in english. It is listed in DOAJ according to the sources read. Declared review time at DOAJ: 15 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- SAGE Publishing
- ISSN
- 2633-0040
- Country
- United Kingdom
- Languages
- english
- Access
- Open access
- Articles in DOAJ
- 140
- Declared review time
- 15 weeks
- Declared peer-review model
- peer_review
- Official website
- https://journals.sagepub.com/home/trd
Index listings
- DOAJ · 2022-05-25
- Indexing
- DOAJ
- APC
- —
- Declared review time (DOAJ)
- 15 weeks — journal-declared only (not measured)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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- Choose your university and rank below ↓
Methodology signals (dated facts from their sources)
Details of the evaluation under the published methodology are shown to signed-in users (free).
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Articles in DOAJ
140
Most recent article
last month
Average review time (journal-declared via DOAJ)
15weeks
Works in OpenAlex
131
Last recorded publication year
2026
h-index
14
i10-index
19
From OpenAlex open data (CC0).
Editorial & policy12
- Last DOAJ review date
- 2024-04-04
- Added to DOAJ
- 2022-05-25
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSS
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Open references deposited at Crossref
- 85%
- ORCID iDs in current deposits
- 82%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 9918557474706676
Classification2
Subjects (DOAJ)
LCC codes
Subject areas
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Lysosomal Storage Disorders Research
- Lysosomal Storage Disorders Research
- Mitochondrial Function and Pathology
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Health Systems, Economic Evaluations, Quality of Life
Show all subjects (50)
- Health Systems, Economic Evaluations, Quality of Life
- Mitochondrial Function and Pathology
- Glycogen Storage Diseases and Myoclonus
- Glycogen Storage Diseases and Myoclonus
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Hemophilia Treatment and Research
- Cellular transport and secretion
- CRISPR and Genetic Engineering
- Genomic variations and chromosomal abnormalities
- Hemophilia Treatment and Research
- Autoimmune and Inflammatory Disorders Research
- Genomic variations and chromosomal abnormalities
- CRISPR and Genetic Engineering
- Cellular transport and secretion
- Autoimmune and Inflammatory Disorders Research
- Biomedical Ethics and Regulation
- Hereditary Neurological Disorders
- Autism Spectrum Disorder Research
- Vasculitis and related conditions
- Hereditary Neurological Disorders
- Autism Spectrum Disorder Research
- Retinal Development and Disorders
- Congenital heart defects research
- Retinal Development and Disorders
- Cystic Fibrosis Research Advances
- Vasculitis and related conditions
- Cystic Fibrosis Research Advances
- Congenital heart defects research
- Biomedical Ethics and Regulation
- Virus-based gene therapy research
- Renal Diseases and Glomerulopathies
- Epilepsy research and treatment
- Connexins and lens biology
- Renal Diseases and Glomerulopathies
- Parathyroid Disorders and Treatments
- Epilepsy research and treatment
- Virus-based gene therapy research
Keywords (DOAJ)
- rare diseases
- genetics
- clinical medicine
- clinical and molecular aspects of rare diseases
- medicine
Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.
The journal's record in other sources:Web of Science MJLDOAJ