ResearchGuide Logo

Chat support

Advanced search ?

Discover the optimal journal based on multiple criteria or locate authors along with their published articles and the corresponding journals.

Publisher

* You can search a publisher or tap the name directly

Subject Area

* You can search a subject area or tap the name directly

Open Acess

Quartille





Genetics in Medicine Open

VERIFIED JOURNAL
You want to contribute ? Login first and send us the Journal infos you think is correct.
We would be pleased to have your collaboration

This journal is included in the ResearchGuide whitelist of reputable titles. Learn more here.

JOURNAL INFORMATION
Open Access YES
E-ISSN 2949-7744
Area Genetics
SCOPE

Genetics in Medicine Open (GIM 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 diversity, equity, and inclusion and uses a double anonymous review process for submitted manuscripts.

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.

Summary

  1. It is an oppen access journal
  2. The Subject Area : Genetics

Guide page

Visit the Journal "Genetics in Medicine Open" Guide
Latest Articles published

Last updated: 22/09/2024

The impact of sphingomyelin on the pathophysiology and treatment response to olipudase alfa in acid sphingomyelinase deficiency


Last updated: 22/09/2024

Health-related quality of life in patients with diverse rare diseases: An online survey


Last updated: 21/09/2024

Expanded-access use of elamipretide in a critically ill patient with Barth syndrome


Last updated: 15/09/2024

Automated fingerprint analysis as a diagnostic tool for the genetic disorder Kabuki syndrome


Last updated: 07/09/2024

ARID1B-related disorder in 87 adults: Natural history and self-sustainability


Last updated: 05/09/2024

Genetic counselors’ perspectives on genomic screening of apparently healthy newborns in the United States


Last updated: 05/09/2024

Genetic kidney disease has a higher likelihood and cost of inpatient admissions compared to other aetiologies


Last updated: 04/09/2024

Ascertainment of uninterrupted CAG repeat length and disease-modifying variants in fragment-based genetic testing for Huntington Disease


Last updated: 25/08/2024

Integration of validated functional evidence to support the pathogenicity of KCNH2 variants


Last updated: 22/08/2024

Variant reclassification and recontact research: A scoping review