Future Rare Diseases

Taylor & Francis Group

Journal websitePeer review: Double-blind review
Evaluation status available after sign-in

About the journal

Future Rare Diseases is an open-access journal published by Taylor & Francis Group in United Kingdom, publishing in english. It is listed in DOAJ according to the sources read. Declared publication charge: 7,678 AUD. Declared review time at DOAJ: 30 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.

Basic facts

Publisher
Taylor & Francis Group
ISSN
2399-5270
Country
United Kingdom
Languages
english
Access
Open access
Declared publication charge
7,678 AUD
Articles in DOAJ
11
Declared review time
30 weeks
Declared peer-review model
double_blind

Index listings

  • DOAJ · 2026-04-22
Indexing
DOAJ
APC
7,678 AUD
Declared review time (DOAJ)
30 weeks — journal-declared only (not measured)
Activity (OpenAlex)
Active — latest works 2026
PublishLens list status
Shown after sign-in
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Methodology signals (dated facts from their sources)

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Journal profile

Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.

Articles in DOAJ

11

Most recent article

last month

Average review time (journal-declared via DOAJ)

30weeks

Works in OpenAlex

143

Last recorded publication year

2026

Reported by OpenAlex in 2 of 3 sources (CC0 flags, not verified indexing)DOAJSciELOOpenAlex Core

h-index

7

i10-index

5

From OpenAlex open data (CC0).

Editorial & policy12
Added to DOAJ
2026-04-22
Declared plagiarism screening
Declared
Other fees beyond APC
No
Declared digital preservation
CLOCKSSPortico
Observed digital preservation (Keepers registry)— snapshot 2026-09-21
CLOCKSSPortico
Editorial board
Official page ↗
Norwegian register (HK-dir)— 2026
Level 1 — approved scholarly channel
Open references deposited at Crossref
38%
ORCID iDs in current deposits
40%
Enrolled in Crossref Similarity Check
✓
Deposits licence metadata at Crossref
✓
APC waiver policy
View policy
Peer-review policy
View policy
Identity & continuity1
Source type
journal
Classification2

Subjects (DOAJ)

Medicine: Internal medicine: Infectious and parasitic diseases

LCC codes

RC109-216

Subject areas

  • Lysosomal Storage Disorders Research
  • Lysosomal Storage Disorders Research
  • Genomics and Rare Diseases
  • Genomics and Rare Diseases
  • Genetics and Neurodevelopmental Disorders
  • Genetics and Neurodevelopmental Disorders
  • Renal Diseases and Glomerulopathies
  • Renal Diseases and Glomerulopathies
Show all subjects (50)
  • Family and Disability Support Research
  • Family and Disability Support Research
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Hemophilia Treatment and Research
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Hemophilia Treatment and Research
  • Complement system in diseases
  • Complement system in diseases
  • Autism Spectrum Disorder Research
  • Blood groups and transfusion
  • Metabolism and Genetic Disorders
  • Autism Spectrum Disorder Research
  • Metabolism and Genetic Disorders
  • Connective tissue disorders research
  • Blood groups and transfusion
  • Connective tissue disorders research
  • Medical Imaging and Pathology Studies
  • Health Systems, Economic Evaluations, Quality of Life
  • Medical Imaging and Pathology Studies
  • Health Systems, Economic Evaluations, Quality of Life
  • Bone Tumor Diagnosis and Treatments
  • Cystic Fibrosis Research Advances
  • Platelet Disorders and Treatments
  • Hemoglobinopathies and Related Disorders
  • Erythrocyte Function and Pathophysiology
  • Pituitary Gland Disorders and Treatments
  • Child Nutrition and Feeding Issues
  • Heterotopic Ossification and Related Conditions
  • Glycogen Storage Diseases and Myoclonus
  • Erythrocyte Function and Pathophysiology
  • Bone Tumor Diagnosis and Treatments
  • Pituitary Gland Disorders and Treatments
  • Platelet Disorders and Treatments
  • Cystic Fibrosis Research Advances
  • Hemoglobinopathies and Related Disorders
  • Gallbladder and Bile Duct Disorders
  • Gallbladder and Bile Duct Disorders
  • Child Nutrition and Feeding Issues
  • Heterotopic Ossification and Related Conditions
  • Glycogen Storage Diseases and Myoclonus
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Chronic Obstructive Pulmonary Disease (COPD) Research

Keywords (DOAJ)

  • rare diseases
  • clinical disease management
  • diagnosis
  • genetic disorders
  • patient advocacy
  • orphan drugs

Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.

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The journal's record in other sources:Web of Science MJLDOAJ

Everything shown here is produced automatically from named sources (DOAJ, OpenAlex, Crossref, PubMed, the Norwegian register) as of its capture date, with no human editing. Facts appear as recorded at the source; derived scores (PCI, PTD, PublishLens score) follow a published methodology. Not a judgement on the journal, not an official accreditation, not advice.

Wrong items are corrected automatically by re-reading the source (24 h for daily sources, 7 days for weekly ones) with a dated change log, and each item links to its source record. PublishLens-derived assessments are contested through the appeals mechanism (15 working days). Appeals · Indicator guide

Norwegian register data: Kanalregisteret (HK-dir, Norway) — CC BY 4.0 / NLOD — adapted: level extracted per year · OASPA member list — CC BY

Last automated source read: