(ISSN 2577-5790)
OBM Genetics is an international Open Access journal published quarterly online by LIDSEN Publishing Inc. It accepts papers addressing basic and medical aspects of genetics and epigenetics and also ethical, legal and social issues. Coverage includes clinical, developmental, diagnostic, evolutionary, genomic, mitochondrial, molecular, oncological, population and reproductive aspects. It publishes a variety of article types (Original Research, Review, Communication, Opinion, Comment, Conference Report, Technical Note, Book Review, etc.). There is no restriction on the length of the papers and we encourage scientists to publish their results in as much detail as possible.
Publication Speed (median values for papers published in 2023): Submission to First Decision: 5.1 weeks; Submission to Acceptance: 17.0 weeks; Acceptance to Publication: 7 days (1-2 days of FREE language polishing included)
Special Issue
Precision Medicine and Gene Sequencing
Submission Deadline: December 31, 2025 (Open) Submit Now
Guest Editor
Sajad Karampoor, PhD
1. Department of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
2. Gastrointestinal and Liver Diseases Research Center, Iran University of Medical Sciences, Tehran, Iran
Research Interests: Virology; immunology; cancer genomics; autoimmune diseases; bioinformatics
About This Topic
The special issue "Precision Medicine and Gene Sequencing" focuses on the transformative potential of genetic and genomic technologies in tailoring medical care to individual patients. Precision medicine leverages advances in gene sequencing to identify genetic variants that influence disease susceptibility, progression, and response to treatment. This approach represents a paradigm shift from conventional medical practices to more personalized, predictive, and preventative healthcare solutions.
By exploring cutting-edge research in gene sequencing technologies, bioinformatics, and clinical applications, this special issue aims to highlight the latest innovations and challenges in integrating genomic data into clinical practice. Topics of interest include novel sequencing methodologies, genetic biomarkers, ethical considerations, and the role of AI in interpreting complex genomic data. We invite contributions from researchers and clinicians that address these aspects, fostering collaboration across disciplines to advance precision medicine. This collection seeks to provide a platform for groundbreaking studies and insights, accelerating progress toward a future of more effective, individualized patient care.
Keywords
Precision medicine; gene sequencing; next-generation sequencing (NGS); pharmacogenomics; artificial intelligence in genomics; genetic diagnostics
Manuscript Submission Information
Manuscripts should be submitted through the LIDSEN Submission System. Detailed information on manuscript preparation and submission is available in the Instructions for Authors. All submitted articles will be thoroughly refereed through a single-blind peer-review process and will be processed following the Editorial Process and Quality Control policy. Upon acceptance, the article will be immediately published in a regular issue of the journal and will be listed together on the special issue website, with a label that the article belongs to the Special Issue. LIDSEN distributes articles under the Creative Commons Attribution (CC BY 4.0) License in an open-access model. The authors own the copyright to the article, and the article can be free to access, distribute, and reuse provided that the original work is correctly cited.
Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). Research articles and review articles are highly invited. Authors are encouraged to send the tentative title and abstract of the planned paper to the Editorial Office (genetics@lidsen.com) for record. If you have any questions, please do not hesitate to contact the Editorial Office.
Welcome your submission!
2023 | ||
CiteScore | SJR | SNIP |
0.4 | 0.160 | 0.093 |
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