Exploring Heterogeneity in Genome-Wide Association Studies

A special issue of Genes (ISSN 2073-4425). This special issue belongs to the section "Molecular Genetics and Genomics".

Deadline for manuscript submissions: closed (20 July 2024) | Viewed by 452

Special Issue Editor


E-Mail Website
Guest Editor
Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA
Interests: electronic health records; genomics; genome-wide association studies; rare variant association studies; phenome wide association studies; women's health; epistasis; genetic epidemiology

Special Issue Information

Dear Colleagues,

"Exploring Heterogeneity in Genome-Wide Association Studies" is a research area that seeks to understand the differences in genetic susceptibility to complex diseases across populations. Genome-wide association studies (GWAS) are widely used to identify disease-associated genetic variants. However, these studies can reveal different results depending on the populations studied, leading to a need for further exploration of heterogeneity. Exploring heterogeneity in GWAS can help identify populations at risk for specific diseases, allowing for earlier diagnosis and intervention and improving precision medicine. This research area aims to identify sources of variability in GWAS results, including differences in sex, ancestry, environmental exposures, and gene–environment interactions, to inform a complete understanding of the genetic architecture of complex diseases. 

Dr. Shefali Setia Verma
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Genes is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • gene–environment interactions
  • sex-stratified
  • ancestry-stratified
  • heterogeneity
  • GWAS
  • precision medicine

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue policies can be found here.

Published Papers

There is no accepted submissions to this special issue at this moment.
Back to TopTop