About the journal
Journal of Sickle Cell Disease is an open-access journal published by Oxford University Press in United Kingdom, publishing in english. It is listed in DOAJ according to the sources read. Declared publication charge: 2,500 USD. 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
- Oxford University Press
- ISSN
- 3029-0473
- Country
- United Kingdom
- Languages
- english
- Access
- Open access
- Declared publication charge
- 2,500 USD
- Articles in DOAJ
- 0
- Declared review time
- 15 weeks
- Declared peer-review model
- peer_review
- Official website
- https://academic.oup.com/jscd
Index listings
- DOAJ · 2026-01-20
- Indexing
- DOAJ
- APC
- 2,500 USD
- 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)
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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
0
Average review time (journal-declared via DOAJ)
15weeks
Works in OpenAlex
267
Last recorded publication year
2026
h-index
3
i10-index
0
From OpenAlex open data (CC0).
Editorial & policy11
- Added to DOAJ
- 2026-01-20
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- LOCKSS
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Open references deposited at Crossref
- 31%
- ORCID iDs in current deposits
- 32%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity3
- Alternate titles
- Journal of sickle cell disease
- Source type
- journal
- NLM unique ID (PubMed)
- 9918991895506676
Classification2
Subjects (DOAJ)
LCC codes
Subject areas
- Hemoglobinopathies and Related Disorders
- Hemoglobinopathies and Related Disorders
- Iron Metabolism and Disorders
- Iron Metabolism and Disorders
- Blood groups and transfusion
- Blood groups and transfusion
- Hemoglobin structure and function
- Hemoglobin structure and function
Show all subjects (50)
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Adolescent and Pediatric Healthcare
- Adolescent and Pediatric Healthcare
- Prenatal Screening and Diagnostics
- Bone and Joint Diseases
- Bone and Joint Diseases
- Prenatal Screening and Diagnostics
- Erythrocyte Function and Pathophysiology
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Food Security and Health in Diverse Populations
- Erythrocyte Function and Pathophysiology
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Food Security and Health in Diverse Populations
- HIV/AIDS Research and Interventions
- HIV/AIDS Research and Interventions
- Neonatal Health and Biochemistry
- Neonatal Health and Biochemistry
- Epilepsy research and treatment
- Acute Myeloid Leukemia Research
- Psychosomatic Disorders and Their Treatments
- Race, Genetics, and Society
- Biotechnology and Related Fields
- Global Health and Surgery
- Psychosomatic Disorders and Their Treatments
- Epilepsy research and treatment
- Acute Myeloid Leukemia Research
- Race, Genetics, and Society
- Global Health and Surgery
- Biotechnology and Related Fields
- Childhood Cancer Survivors' Quality of Life
- Epigenetics and DNA Methylation
- Neurogenetic and Muscular Disorders Research
- Chronic Disease Management Strategies
- Pain Management and Opioid Use
- Childhood Cancer Survivors' Quality of Life
- Epigenetics and DNA Methylation
- Neurogenetic and Muscular Disorders Research
- Chronic Disease Management Strategies
- Pain Management and Opioid Use
- Palliative Care and End-of-Life Issues
- Palliative Care and End-of-Life Issues
Keywords (DOAJ)
- sickle cell disease
- sickle cell trait
- genetic modifiers
- holistic disease
- translational research
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