Genetics Society of America
GSA connects you to the field through a range of scholarly and community publications: our peer-reviewed journals offer two distinct platforms for communicating high-quality original research; our blog brings perspective to your research and career; and our newsletters keep you up to date with the latest opportunities and news from your community.
GENETICS publishes high-quality genetics and genomics research that expands scientific boundaries—we’ve been building the field since 1916. With its broad readership, rich history, and responsive editors, GENETICS brings the latest in publishing innovations to the communities it serves. We invite you to submit your research and discover the fast turnaround times and helpful review process for yourself.
Get your useful data out into the world by publishing in G3: Genes|Genomes|Genetics. G3 publishes high quality foundational research, particularly studies that generate useful genetic information, such as mutant screens, single gene studies, genome maps, genome sequence data, GWAS and QTL studies, software, data resources, and new methods. The Editorial Board of G3 believes that rapid dissemination of such data lays the foundation for many important insights.
We treat authors as colleagues, not adversaries. Your time is important—and so is your research. Peer editors oversee the review process and give you clear guidance on how to address any reviewer comments; our helpful editorial staff keep the process moving and on time. We make it easy to submit: no formatting requirements on initial submission. Our dedicated editors work hard to keep time to first decision at around a month. And because we’re agile and community-driven, we’ve long been at the forefront of publishing innovations.
The GSA Journals are committed to helping authors get their work in front a wide audience. Our Promotional Toolkit for Authors contains pointers to help you promote your GENETICS or G3: Genes|Genomes|Genetics paper, including how GSA and Oxford University Press can help.
The review experience has been the single most useful and pleasant of my career. The reviews were constructive and fair, the editor provided exceptionally clear guidance, and turn-around on the revision was lightning fast.
Genes to Genomes, the GSA blog, features news from the GSA community, highlights from the GSA journals, and posts from staff and guest authors about careers, professional development, science policy, publishing, education, outreach, equity and inclusion, and the intersections of science, art, and culture. Propose a guest post yourself and start a conversation!
In March 2016, GENETICS launched WormBook, a comprehensive compendium of review articles presenting the current state of knowledge in C. elegans research. WormBook articles span the breadth of the biology, genetics, genomics, and evolutionary biology of C. elegans. Find historical WormBook articles published as the online companion to WormBase here. This page contains the full list of all historical and GSA-published WormBook articles, organized by section.
Interviews from newly appointed faculty members shed light on the path to landing a faculty position.
AbstractC. elegans insulin/insulin-like growth factor 1 signaling, IIS, affects diverse physiological processes through the DAF-16/FOXO transcription factor. Despite its ubiquitous presence in somatic cells, DAF-16’s effects exhibit prevalent tissue specificity as well as tissue crosstalk. This implies that tissue-specific DAF-16 transcriptional programs contribute to functional diversity of IIS. To further investigate this possibility, we sought muscle-cell-specific DAF-16 transcriptional targets. Using fluorescence-activated cell sorting to enrich for body wall muscle cells from young hermaphroditic adults, we...
AbstractOne of the front-line drug classes used to treat invasive fungal infections is echinocandins, which target the fungal-specific beta-glucan synthase (Fks). Treatment failure due to resistance often coincides with mutations in three protein regions defined as hotspots. Unfortunately, the scarcity of the mutational data reported, combined with the large size and membrane-embedded nature of the enzyme hinder any effort to characterize genotype-phenotype links. Recent advances in solving the structure of Fks bring us one step...
