About the journal
Rare is an open-access journal published by Elsevier in Netherlands, publishing in english. It is listed in DOAJ according to the sources read. Declared publication charge: 915 USD. Declared review time at DOAJ: 21 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Elsevier
- ISSN
- 2950-0087
- Country
- Netherlands
- Languages
- english
- Access
- Open access
- Declared publication charge
- 915 USD
- Articles in DOAJ
- 115
- Declared review time
- 21 weeks
- Declared peer-review model
- double_blind
- Official website
- https://www.sciencedirect.com/journal/rare
Index listings
- DOAJ · 2024-06-20
- Indexing
- DOAJ
- APC
- 915 USD
- Declared review time (DOAJ)
- 21 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)
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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
115
Most recent article
3 months ago
Average review time (journal-declared via DOAJ)
21weeks
Works in OpenAlex
134
Last recorded publication year
2026
h-index
7
i10-index
2
From OpenAlex open data (CC0).
Editorial & policy11
- Last DOAJ review date
- 2026-04-27
- Added to DOAJ
- 2024-06-20
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Open references deposited at Crossref
- 86%
- ORCID iDs in current deposits
- 39%
- Deposits licence metadata at Crossref
- ✓
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 9918769583006676
Classification4
Subjects (DOAJ)
LCC codes
Subject areas
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Autism Spectrum Disorder Research
- Autism Spectrum Disorder Research
Show all subjects (50)
- Neurogenetic and Muscular Disorders Research
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
- Health Systems, Economic Evaluations, Quality of Life
- Academic Publishing and Open Access
- Health Systems, Economic Evaluations, Quality of Life
- Magnetic confinement fusion research
- Biomedical and Engineering Education
- Academic Publishing and Open Access
- Biomedical and Engineering Education
- Family and Disability Support Research
- Metabolism and Genetic Disorders
- Biochemical and Molecular Research
- Metabolism and Genetic Disorders
- Biochemical and Molecular Research
- Family and Disability Support Research
- Social Media in Health Education
- Mitochondrial Function and Pathology
- Connective tissue disorders research
- Congenital heart defects research
- Diet and metabolism studies
- Genetic factors in colorectal cancer
- Lysosomal Storage Disorders Research
- Prenatal Screening and Diagnostics
- Chronic Lymphocytic Leukemia Research
- Glycogen Storage Diseases and Myoclonus
- Trace Elements in Health
- Dust and Plasma Wave Phenomena
- Social Media in Health Education
- Mitochondrial Function and Pathology
- RNA regulation and disease
- Congenital heart defects research
- Connective tissue disorders research
- Lysosomal Storage Disorders Research
- Glycogen Storage Diseases and Myoclonus
- Diet and metabolism studies
- Genetic factors in colorectal cancer
- Chronic Lymphocytic Leukemia Research
- Prenatal Screening and Diagnostics
- Hereditary Neurological Disorders
- Trace Elements in Health
Keywords (DOAJ)
- undiagnosed disease
- rare disease
- patients’ care
- genetics
- orphan drugs
- phenotyping
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