Molecular Genetics and Genetic Diseases
A section of Biomedicines (ISSN 2227-9059).
Section Information
The section “Molecular Genetics and Genetic Diseases” covers the basic and translational aspects of human genetic diseases and genomics research, from fundamental molecular investigation to preclinical animal models. In particular, this section aims to facilitate the rapid publication of innovative research encompassing the genetic basis of human health and disease, as well as the treatment of genetic disorders, and heritable or acquired cancers. We welcome submissions that apply new and emerging technologies in the fields of genomics, transcriptomics and bioinformatic tools to advance knowledge in human genetic diseases.
Topics within the scope of this section include, but are not limited to:
- Chromosome organization, structure, and function; chromatin remodeling and dynamics, chromosomal maintenance elements;
- DNA replication, repair, recombination, mobile DNA, mitochondrial DNA;
- DNA methylation, histone modification, histone code;
- RNA biology, transcription and splicing, coding and non-coding RNA analysis, RNA localization, translation and catalysis by RNA;
- Post-transcriptional regulation of gene expression;
- Genetic toxicology and environmental mutagenesis;
- Genetics of monogenic diseases and complex diseases; genotype–phenotype relationships;
- Precision medicine; pharmacogenetics and pharmacogenomics;
- Targeted genome editing; gene therapy and delivery systems; genetically-engineered cell therapy
- RNA and small nucleic acid-based therapeutics;
- Genetic testing and molecular diagnostics; biomarker development and application; genome-wide association studies;
- Epigenetic therapy; cancer immunotherapy;
- Developmental genetics; epigenetics and epigenomics.
Editorial Board
Topical Advisory Panel
Special Issues
Following special issues within this section are currently open for submissions:
- Noncoding RNAs (ncRNAs): The Role in Gene Regulation and Human Diseases (Deadline: 31 December 2024)
- Innovations and Prospects in Single Cell RNA-seq for Biomedical Research (Deadline: 31 January 2025)
- Genetic and Molecular Mechanisms of Cardiometabolic Diseases and Cancers—2nd Edition (Deadline: 31 January 2025)
- Kidney Disease: From Pathophysiology to Novel Therapeutic Approaches (3rd Edition) (Deadline: 31 January 2025)
- Genetic and Epigenetics of Kidney Development: Pathologies of Renal Anomalies and Kidney Diseases (Deadline: 31 January 2025)
- Mitochondrial Dysfunction and Reactive Oxygen Species in Aging and Related Diseases (Deadline: 28 February 2025)
- Unraveling the Epigenetic Blueprint: Exploring DNA Methylation and Its Integration with Omics in Health and Disease (Deadline: 28 February 2025)
- Immunogenetic Regulations for Disease Prognosis (Deadline: 28 February 2025)
- From Gene Variant to Variant Function: Recent Advances in Cancer Genetics (Deadline: 28 February 2025)
- Gene Delivery and Gene Editing (Deadline: 31 March 2025)
- Advances and Applications of Regulatory Genomics in Multiple Myeloma (Deadline: 31 March 2025)
- Molecular Biomarkers of Tumors: Advancing Genetic Studies (Deadline: 31 March 2025)
- Molecular Processes Underlying Pathogenesis and Advanced Therapies for Genodermatosis (Deadline: 30 April 2025)
- Genetic Research on Neuropsychiatric Disorders and Complex Human Diseases (Deadline: 30 April 2025)
- Exploring Human Diseases through Genomic and Genetic Analyses (Deadline: 30 April 2025)
- Bioinformatics Analysis of miRNA for Human Health and Disease (Deadline: 30 April 2025)
- Epigenetic Regulation in Cancer Progression (Deadline: 30 April 2025)