Genetics in Medicine Open

Published by Elsevier

Open access · CC BY-NC-ND · In DOAJ · United States · Genomics and Rare Diseases

Journal at a glance

ISSN

29497744

Publisher

Elsevier

Country

United States

Language

en

License

CC BY-NC-ND

Also known as: Genet Med Open (Abbreviation), GIM open (Alternate title)

Indexing

• DOAJ: Active
• Scopus: Indexed
• Pubmed: Active

Metrics

Subjects

• Genomics and Rare Diseases
• BRCA gene mutations in cancer
• Genomic variations and chromosomal abnormalities
• Metabolism and Genetic Disorders
• Prenatal Screening and Diagnostics
• Cancer Genomics and Diagnostics
• Connective tissue disorders research
• Science: Biology (General): Genetics
• Medicine
• Genetics
• Biology

Articles on PubPorta

The most recent records PubPorta holds for this journal.

• Population-Specific Optimization of Polygenic Risk Scores for Breast Cancer in East Asians (2026)
• AI-Assisted Clinical Exome Sequencing: Insights and Outcomes from 822 Pediatric Diagnoses (2026)
• Socioeconomic and Clinical Factors Associated with Genetic Testing Completion in Stargardt Disease (2026)
• Envisioning a more equitable and economical future for genomic testing (2026)
• Advocating for Professional Guidance on Medical Updates in Gamete Donation: A Perspective from US-Based Genetic Counselors (2026)

Similar journals

• Journal of Medical Genetics — United Kingdom · — · Same subject: BRCA gene mutations in cancer, Same subject: Connective tissue disorders research, 5 shared subjects in total
• Application of Clinical Genetics — New Zealand · Open access · Same subject: BRCA gene mutations in cancer, Same subject: Genomic variations and chromosomal abnormalities, 5 shared subjects in total
• European Journal of Human Genetics — United Kingdom · — · Same subject: BRCA gene mutations in cancer, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total
• European Journal of Medical Genetics — France · — · Same subject: Connective tissue disorders research, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total
• Clinical Dysmorphology — United Kingdom · — · Same subject: Connective tissue disorders research, Same subject: Genomic variations and chromosomal abnormalities, 4 shared subjects in total
• Orphanet Journal of Rare Diseases — United Kingdom · Open access · Same subject: Connective tissue disorders research, Same subject: Genomics and Rare Diseases, 3 shared subjects in total

Sources: DOAJ, NLM Catalog, OpenAlex, Crossref, Scopus · Last verified 2026-06-29

Author guidelines