Molecular Genetics & Genomic Medicine is a peer-reviewed journal aimed at the rapid dissemination of high-quality research related to human, molecular, and medical genetics. The journal publishes original research articles covering discoveries in the phenotypic, molecular, and genomic aspects of genomic variation, hereditary diseases, and birth defects. Its broad scope includes both rare and common diseases, from diagnosis to treatment. Examples of suitable articles include reports of new disease genes, functional studies of genetic variations, in-depth genotype-phenotype studies, genomic analyses of hereditary diseases, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and clinical diagnostic approaches. Molecular Genetics & Genomic Medicine provides a scientific foundation for next-generation sequencing research on rare and common diseases, enabling the scientific community to easily and quickly access research in this fascinating field. This serves as the basis for translating next-generation sequencing research into personalized diagnostics and treatments for everyday healthcare. The journal publishes original research articles, reviews, and methodological papers, as well as invited editorials and commentaries. Original research papers must report well-designed studies and provide data-supported conclusions.