Journal of Medical Genetics : Impact Factor & More
eISSN: 1468-6244pISSN: 0022-2593
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Aims and Scope of Journal of Medical Genetics
The Journal of Medical Genetics is a leading international peer-reviewed medical journal covering original research in human genetics, including reviews of and opinion on the latest developments. Articles cover the molecular basis of human disease including germline cancer genetics, clinical manifestations of genetic disorders, applications of molecular genetics to medical practice and the systematic evaluation of such applications worldwide. It was established in September 1964 and is published by the BMJ Group. The editor-in-chief is Huw Dorkins (University of Oxford). Less
Key Metrics
CiteScore 
10.1
Eigenfactor
0.01 - 0.05
H-Index
185
Impact Factor
< 5
SJR
Q1Genetics
SNIP
1.73
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Topics Covered on Journal of Medical Genetics
Journal of Medical Genetics Journal Specifications
Indexed in the following public directories
Web of Science 
Scopus 
SJR
| Overview | |
| Publisher | BMJ PUBLISHING GROUP |
| Language | English |
| Frequency | Monthly |
| General Details | |
| Language | English |
| Frequency | Monthly |
| Publication Start Year | 1964 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Journal of Medical Genetics
Longest surviving patient with a homozygous splice-altering EGFR pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.
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Review of estimates of birth incidence and population prevalence over time and between countries of the rare neurodevelopmental condition Prader-Willi syndrome.
- 5 Jun 2026
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Longest surviving patient with a homozygous splice-altering EGFR pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.
- 30 Jun 2026
- Journal of medical genetics
Functional characterisation and pathological significance of variants of MEF2C promoter in tetralogy of Fallot.
- 29 Jun 2026
- Journal of medical genetics
Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.
- 19 Jun 2026
- Journal of medical genetics
Interpreting TP53 variants: somatic mosaicism and ERCC6L2-driven clonal evolution.
- 9 Jun 2026
- Journal of medical genetics
Biallelic pathogenic variants in FLNB are associated with paediatric steroid-resistant nephrotic syndrome via podocyte cytoskeletal dysfunction.
- 8 Jun 2026
- Journal of medical genetics
Review of estimates of birth incidence and population prevalence over time and between countries of the rare neurodevelopmental condition Prader-Willi syndrome.
- 5 Jun 2026
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