Personalized Medicine

Future Medicine

Evaluation status available after sign-in

About the journal

Personalized Medicine is a journal published by Future Medicine in United Kingdom. It is listed in MEDLINE and PUBMED according to the sources read. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.

Basic facts

Publisher
Future Medicine
ISSN
1741-0541 · 1744-828X
Country
United Kingdom
Access
Not open access / not declared

Index listings

  • MEDLINE · 2018-01-01
  • PUBMED · 2004-12-01
Indexing
MEDLINE · PUBMED
APC
—
Declared review time (DOAJ)
—
Activity (OpenAlex)
Active — latest works 2026
PublishLens list status
Shown after sign-in
Counts for promotion at your university?
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).

Create a free account to view the evaluation

Journal profile

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

Works in OpenAlex

1516

Last recorded publication year

2025

Reported by OpenAlex in 1 of 3 sources (CC0 flags, not verified indexing)DOAJSciELOOpenAlex Core

h-index

50

i10-index

408

From OpenAlex open data (CC0).

Editorial & policy5
Observed digital preservation (Keepers registry)— snapshot 2026-10-05
CLOCKSSPortico
Norwegian register (HK-dir)— 2026
Level 1 — approved scholarly channel
Open references deposited at Crossref
99%
ORCID iDs in current deposits
43%
Enrolled in Crossref Similarity Check
✓
Deposits licence metadata at Crossref
✓
Identity & continuity2
Source type
journal
NLM unique ID (PubMed)
101238549
Classification(no data)

No data available to the platform for this group

No platform data for: Classification — absence is not a judgment about the journal.

Subject areas

  • Pharmacogenetics and Drug Metabolism
  • BRCA gene mutations in cancer
  • BRCA gene mutations in cancer
  • Genetic Associations and Epidemiology
  • Pharmacogenetics and Drug Metabolism
  • Pharmacogenetics and Drug Metabolism
  • Genomics and Rare Diseases
  • Genomics and Rare Diseases
Show all subjects (75)
  • Genomics and Rare Diseases
  • Nutrition, Genetics, and Disease
  • Cancer Genomics and Diagnostics
  • Cancer Genomics and Diagnostics
  • Cancer Genomics and Diagnostics
  • Ethics in Clinical Research
  • Ethics in Clinical Research
  • Ethics in Clinical Research
  • Science, Research, and Medicine
  • Health Systems, Economic Evaluations, Quality of Life
  • Medical and Health Sciences Research
  • Health Systems, Economic Evaluations, Quality of Life
  • Nutrition, Genetics, and Disease
  • Nutrition, Genetics, and Disease
  • Bioinformatics and Genomic Networks
  • Bioinformatics and Genomic Networks
  • Pharmaceutical Economics and Policy
  • Computational Drug Discovery Methods
  • Computational Drug Discovery Methods
  • Biomedical Ethics and Regulation
  • Artificial Intelligence in Healthcare and Education
  • Biomedical Ethics and Regulation
  • Health Systems, Economic Evaluations, Quality of Life
  • Genetic Associations and Epidemiology
  • Genetic Associations and Epidemiology
  • Ethics and bioethics in healthcare
  • BRCA gene mutations in cancer
  • Biomedical Ethics and Regulation
  • Lung Cancer Treatments and Mutations
  • Technology and Human Factors in Education and Health
  • Biomedical and Engineering Education
  • Biomedical and Engineering Education
  • Genetics, Bioinformatics, and Biomedical Research
  • Genetics, Bioinformatics, and Biomedical Research
  • Lung Cancer Treatments and Mutations
  • Lung Cancer Treatments and Mutations
  • Genetic factors in colorectal cancer
  • Genetic factors in colorectal cancer
  • Genetics, Bioinformatics, and Biomedical Research
  • Health and Medical Research Impacts
  • Biotechnology and Related Fields
  • Biotechnology and Related Fields
  • Health and Medical Research Impacts
  • Human auditory perception and evaluation
  • Human auditory perception and evaluation
  • Diverse Scientific and Economic Studies
  • Breast Cancer Treatment Studies
  • Diverse Scientific and Economic Studies
  • Science, Research, and Medicine
  • Science, Research, and Medicine
  • Colorectal Cancer Treatments and Studies
  • MicroRNA in disease regulation
  • Colorectal Cancer Treatments and Studies
  • Educational Robotics and Engineering
  • Electronic Health Records Systems
  • Educational Robotics and Engineering
  • Race, Genetics, and Society
  • Pharmaceutical studies and practices
  • Pharmaceutical studies and practices
  • MicroRNA in disease regulation
  • Health, Environment, Cognitive Aging
  • CRISPR and Genetic Engineering
  • CRISPR and Genetic Engineering
  • MicroRNA in disease regulation
  • Drug-Induced Adverse Reactions
  • Innovations in Medical Education
  • Cancer-related molecular mechanisms research

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

Loading community confirmations…
How do we evaluate?Publisher of this journal? Appeal a derived assessment or request a factual correction

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: