Personalized Medicine
Published by Taylor & Francis Group
United Kingdom · BRCA gene mutations in cancer
Journal at a glance
- ISSN
- 1741-0541
- Publisher
- Taylor & Francis Group
- Country
- United Kingdom
- Language
- en
Also known as: Per Med (Abbreviation)
Indexing
- Web of Science (SCIE): Indexed
- Scopus: Indexed
- Medline: Active
- Pubmed: Active
Metrics
| Metric | Value | Year | Source |
|---|
| h-index (OpenAlex) | 50 | 2026 | OpenAlex |
| i10-index (OpenAlex) | 413 | 2026 | OpenAlex |
| Works (OpenAlex) | 1519 | 2026 | OpenAlex |
| DOIs registered (Crossref) | 1486 | 2026 | Crossref |
| DOIs, current year (Crossref) | 122 | 2026 | Crossref |
| Citations (OpenAlex) | 15911 | 2026 | OpenAlex |
| 2-year mean citedness (OpenAlex) | 1.256 | 2026 | OpenAlex |
Subjects
- BRCA gene mutations in cancer
- Pharmacogenetics and Drug Metabolism
- Genomics and Rare Diseases
- Cancer Genomics and Diagnostics
- Ethics in Clinical Research
- Health Systems, Economic Evaluations, Quality of Life
- Nutrition, Genetics, and Disease
Articles on PubPorta
The most recent records PubPorta holds for this journal.
Similar journals
- Familial Cancer — Kingdom of the Netherlands · — · Same subject: BRCA gene mutations in cancer, Same subject: Cancer Genomics and Diagnostics, 3 shared subjects in total
- Molecular Diagnosis and Therapy — Switzerland · — · Same subject: Cancer Genomics and Diagnostics, Same subject: Genomics and Rare Diseases, 3 shared subjects in total
- Hereditary Cancer in Clinical Practice — Poland · Open access · Same subject: BRCA gene mutations in cancer, Same subject: Cancer Genomics and Diagnostics, 3 shared subjects in total
- Rare — Open access · Same subject: BRCA gene mutations in cancer, Same subject: Genomics and Rare Diseases, 3 shared subjects in total
- Trials — United Kingdom · Open access · Same subject: Ethics in Clinical Research, Same subject: Health Systems, Economic Evaluations, Quality of Life, Same country
- Journal of Medical Genetics — United Kingdom · — · Same subject: BRCA gene mutations in cancer, Same subject: Genomics and Rare Diseases, Same country
Sources: OpenAlex, NLM Catalog, Crossref, Web of Science (Clarivate), Scopus · Last verified 2026-09-05