Our July Issue has been released! On the cover: "Preparing for Patient-Customized N-of-1 Antisense Oligonucleotide Therapy to Treat Rare Diseases" by Harry Wilton-Clark, Eric Y. and Prof. Toshifumi Yokota Browse the whole issue at: https://lnkd.in/dAejh5X6
Genes MDPI
Book and Periodical Publishing
Genes (ISSN 2073-4425, IF 4.141), an Open Access journal of genetics and genomics published online by MDPI.
About us
Genes (ISSN 2073-4425, IF 2.8), an international, peer-reviewed open access journal on genetics and genomics who publishes reviews, research articles, communications and technical notes on the following topics of interest, but are not limited to: • DNA; RNA • genetic code; gene structure; gene expression • chromosomes; recombination and linkage; genetic mapping • transcriptional profiling; analysis of noncoding and other RNAs • cloning; genetically modified organisms • human genetics; medical genetics; gene therapy; personal medicine • population genetics; conservation genetics; phylogenomics; phylogenetics • genome projects; genomics • sequencing technologies; bioinformatics Genes was launched in 2009 and has published more than 11,000 peer-reviewed manuscripts freely available on our website. Our journal is led by more than 700 international editorial board members covering all the fields of genetics and genomics.
- Website
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https://www.mdpi.com/journal/genes
External link for Genes MDPI
- Industry
- Book and Periodical Publishing
- Company size
- 11-50 employees
- Headquarters
- Basel
- Type
- Privately Held
- Founded
- 2009
Locations
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Primary
Sankt-Alban Anlage 66
Basel, 4052, CH
Employees at Genes MDPI
Updates
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Special issue, edited by Dr. Greco Hernandez, aims to discuss the state of the art of key aspects of protein synthesis in cancer initiation, progression, metastasis, and dormancy. Submit your paper at: https://lnkd.in/dvW4Tit4
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Dr. Chandra Shekhar Boosani from University of Missouri-Columbia is guest editing an issue on non-coding RNA-mediated gene regulation in cardiovascular diseases. Read more about this new issue at: 🔗https://lnkd.in/dHeTHKhY
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Most viewed article in our July issue: "Exonic Short Interspersed Nuclear Element Insertion in 𝘍𝘈𝘔161𝘈 Is Associated with Autosomal Recessive Progressive Retinal Atrophy in the English Shepherd" by Dr. Katherine Stanbury from University of Cambridge et al. https://lnkd.in/dBqbn_Cv
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Special Issue, edited by Dr. Mari Mori, will explore the applications of high-throughput sequencing technologies, which have revolutionized our understanding of human health and disease. Send your contribution at: https://lnkd.in/eDW7h9wW
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Genes MDPI reposted this
Breakthrough genetic test to eliminate a form of inherited blindness in dogs. In a study, published in the open access journal Genes MDPI, researchers from the University of Cambridge identify the genetic mutation that causes progressive retinal atrophies (PRAs) in English Shepherd dogs. In addition to this discovery and due to there currently being no cure for PRA, the team also developed a DNA test to identify dogs carrying the disease. The development of a genetic screening test marks a significant advancement, providing dog breeders with the opportunity to safeguard the future health of English Shepherd dogs against developing this blinding disease by reducing the frequency of the disease variant within the breed. Learn more about this research: https://brnw.ch/21wLALT #progressiveretinalatrophy #PRA #openscience #openaccess
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We are excited to announce Prof. Leonardo Reis Da Silva as Guest Editor for an issue that aims to disseminate high quality research on immunotherapy and genomics in the field of genitourinary cancer. Read more about and submit your paper at: https://lnkd.in/eFmwjDT4
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We will attend the ESC Congress, organized by the European Society of Cardiology, held in London, UK, from 30 August to 2 September 2024. We invite all attendees to visit our booth G 160 and share their latest ideas with us. https://lnkd.in/dKCqVCca
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Special Issue, edited by Dr. Binod Kumar from UMass Chan Medical School and Dr. Carlos A. Saavedra-Matiz from New York State Department of Health, will cover the past, present, and future widespread genetic landscape of newborn screening. Submit your contribution at: https://lnkd.in/dF7NYStJ
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Featured on our front page: "The Intriguing Mystery of RPA Phosphorylation in DNA Double-Strand Break Repair" by Valerie Fousek-Schuller and Dr. Gloria Borgstahl from University of Nebraska Medical Center. https://lnkd.in/djyjaytc
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