Genetics in Medicine Open publishes research on genetic diagnoses and variant analysis, including the application of genome sequencing and other molecular techniques for identifying pathogenic or likely pathogenic variants. The journal covers studies on inherited diseases, carrier screening, and the clinical implications of genetic findings, such as cancer risk and developmental disorders. It also explores advancements in genetic testing technologies and their diagnostic yield across different sample types.
Based on the Think.Check.Submit framework by DOAJ, COPE & OASPA. All data from verified open sources.
Publication & Citation Trend
Articles published
Times cited
2023
2024
2025
2026
Source: OpenAlex · Note: citations accumulate over time so older years appear higher
SJR Quartile by Discipline
Scimago ranks this journal separately in each subject category — its quartile can differ by discipline.
Biochemistry, Genetics and Molecular Biology (miscellaneous)Q2
GeneticsQ3
Molecular BiologyQ3
Cell BiologyQ4
Subject Classification
Scopus Categories
GeneticsBiochemistry, Genetics and Molecular Biology (miscellaneous)Cell BiologyMolecular Biology
Research Topics (OpenAlex)
Genomics and Rare DiseasesBRCA gene mutations in cancerGenomic variations and chromosomal abnormalitiesMetabolism and Genetic DisordersPrenatal Screening and DiagnosticsCancer Genomics and DiagnosticsConnective tissue disorders researchGenetic factors in colorectal cancerGenetics and Neurodevelopmental DisordersDiverse Scientific and Economic Studies