Journal of Medical Genetics
is a leading human genetics journal publishing global authoritative research and reviews
Impact Factor: 3.6
Citescore: 7.6
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Journal of Medical Genetics: 60th Anniversary
September 2024 marks an exciting and important milestone for Journal of Medical Genetics as we celebrate 60 years of publishing! Over the past 6 decades, we have established ourselves as a trusted source for robust research.
To celebrate this achievement, we are reflecting on key achievements and highlighting some of the most influential research that the journal has published. Join us in commemorating 60 years of academic excellence, and here's to many more years of impactful publishing!
Read the editorial from Editor-in-Chief, Huw Dorkins: JMG at 60.
Discover the Six at Sixty collection, a series of commentaries by the authors of some of our most widely read articles, reflecting on the work they reported and subsequent developments in that area.
Authors
The Journal of Medical Genetics accepts submissions of a wide range of article types, including original research, review and short reports.
The Author Information section provides specific article requirements to help you turn your research into an article suitable for JMG.
Information is also provided on editorial policies and open access.
Journal of Medical Genetics Learning
In collaboration with BMJ Learning, Journal of Medical Genetics offers high-quality continuing medical education for doctors and other healthcare professionals.
All Journal of Medical Genetics Multiple Choice Questions are listed on BMJ Learning. You can also find a list of our modules by title on our learning hub >>
Our latest module is Extent of investigation and management of cases of ‘unexplained’ mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus
Most Read Articles
Genotype-phenotype correlations:
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome21 February 2024
Clinical guidelines:
Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement21 May 2024
Latest Articles
Cancer genetics:
Protein-truncating and rare missense variants in ATM and CHEK2 and associations with cancer in UK Biobank whole-exome sequence data23 October 2024
Cancer genetics:
Novel germline TP53 variant (p.(Phe109Ile)) confers high risk of cancer23 October 2024
Cancer genetics:
A novel pathogenic germline chromosome 3 inversion in von Hippel-Lindau disease23 October 2024
Blog Posts
29 October 2024
22 October 2024
8 October 2024