Genetics in Medicine Open is an open access journal with a broad focus on medical genetics and genomic medicine, including all aspects of therapy. It has a strong emphasis on global submissions from diverse populations and authors from underrepresented backgrounds. The journal uses a double anonymous review process for submitted manuscripts.

Genetics in Medicine Open
Positioned as an official journal of the American College of Medical Genetics and Genomics and the companion journal of Genetics in Medicine, GIM Open is an international journal publishing scientific works that advance the knowledge, understanding, and practice of medical genetics and genomic medicine for all continents. GIM Open welcomes submissions of Original Research, Reviews, Commentaries and Brief Reports in the areas of clinical genetics, cytogenetics, molecular genetics, biochemical genetics, reproductive medicine, cancer genetics, pharmacogenomics, clinical trials, population genetics, public health, genome-wide association studies, polygenic risk, bioinformatics, methodologies, clinical implementation, ELSI (ethical, legal, and social issues), genetic counseling, and practice standards and guidelines.
GIM Open welcomes submissions of data-driven, hypothesis-based and scientifically rigorous exploratory research that innovates or implements new science and technologies in genomic medicine. Manuscripts reporting animal models providing clinically relevant insights into human disease mechanisms and potential therapeutics are also welcome. Manuscripts of candidate disease gene discoveries based on a small cohort size but solidified by a high standard of scientific rigor, validity, and reproducibility may be considered. Rare case reports may be considered if they fill a knowledge gap in populations underrepresented in genetics research or experiencing health disparities, or inform exceptionally significant actionability in diagnosis, prognosis, and therapeutics. GIM Open promotes studies that include diverse, especially under-represented, populations.
Latest Articles
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Issue 2949-7744
“It is important to me to know where the information is going”: Views of adults with intellectual disability on data sharing in precision medicine research
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Issue 2949-7744
12-month outcomes of elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA) in rare CFTR missense variant
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Issue 1098-3600
A North Carolina newborn screening pilot for mucopolysaccharidosis II: Evaluating endogenous nonreducing end glycosaminoglycan analysis and IDS sequencing as higher-tier testing options
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Issue 2949-7744
A population-representative survey on attitudes toward genomic newborn screening in Germany
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Issue 1098-3600
AAVC: An automated framework for high-accuracy ACMG-based variant classification
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Issue 2949-7744
ACMG Medical Directors’ Special Interest Group survey: Current challenges for medical genetics clinics
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Issue 1098-3600
ACMG/AMP variant classification specifications from the ClinGen Epilepsy Sodium Channel Variant Curation Expert Panel
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Issue 2949-7744
Advocating for professional guidance on medical updates in gamete donation: A perspective from US-based genetic counselors
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Issue 1098-3600
An economic evaluation of functional genomic testing for individuals with undiagnosed rare disorders
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Issue 1098-3600
An integrated cardiometabolic genetic testing program in a predominantly Hispanic population within a community setting