Aim & Scope
International Journal of Genetics and Genomic Science (ISSN: 2836-2306) is an international, Open Access publisher of peer-reviewed journals encompassing a broad spectrum of scientific research and technological disciplines.
International Journal of Genetics and Genomic Science (ISSN: 2836-2306) is originated with a rigid commitment of serving the scientific and research community by inviting innovations and a vision to encourage the existing scientists, experts and young scientists to enlighten the common society, encompassing a broad spectrum of scientific research and technological disciplines.
International Journal of Genetics and Genomic Science (ISSN: 2836-2306) is an Open Access single blinded peer-reviewed medical journal, publishes original research articles, review papers, clinical studies, case reports, editorials, perspectives, etc. It seeks support from individuals, institutes, libraries, universities, funding agencies, and others.
International Journal of Genetics and Genomic Science (ISSN: 2836-2306) deals with the disorders and complications that are related to genetic mutations, hereditary diseases, genomic variations, molecular genetics, and associated diagnostic and therapeutic approaches.
The current research in the International Journal of Genetics and Genomic Science (ISSN: 2836-2306) involves in the development of new techniques to minimize these ailments and provides knowledge for researchers, practitioners, and even common people.
International Journal of Genetics and Genomic Science (ISSN: 2836-2306) accepts the articles in the fields of: General Genetics, Genomics, Human Genetics, Molecular Genetics, Genomic Medicine, Population Genetics, Evolutionary Genetics, Functional Genomics, Epigenetics, DNA Sequencing, Gene Expression, Genetic Mutations, Inherited Disorders, Single Nucleotide Polymorphisms (SNPs), Rare Genetic Diseases, Cancer Genomics, Neurogenetics (Alzheimer’s, Parkinson’s), Cardiogenomics (Heart Disease & Genetics), Metabolic Disorders (Diabetes, Obesity), Immunogenetics, Next-Generation Sequencing (NGS), CRISPR & Gene Editing, Whole Genome Sequencing, RNA Sequencing (RNA-Seq), Computational Genomics, Systems Biology, Genome-Wide Association Studies (GWAS), Personalized Genomics, Genomic Data Analysis, Pharmacogenomics, Gene Therapy, Personalized Medicine, Cancer Immunogenomics, Biomarkers in Genomic Medicine, Synthetic Biology, Comparative Genomics, Human Evolutionary Genetics, Ancestry & Genetic Lineage, Genetic Diversity, Environmental & Adaptive Genomics, Genetic Privacy & Ethics, Genomic Data Sharing, Genetic Counseling, Ethical Issues in CRISPR, Regulation of Gene Therapy.
Authors can contribute their valuable submission through online and/or to info@mediresonline.org
General Genetics: General genetics is the branch of biology that studies how traits and characteristics are inherited and expressed across generations. It examines genes, DNA structure, genetic variation, and the mechanisms of heredity. The field helps explain how genetic information influences development, health, and evolution.
Genomics: Genomics is the study of the entire set of genes (genome) of an organism, including their structure, function, evolution, and interactions. It involves analyzing DNA sequences to understand how genes influence development, health, and disease at a global, system-wide level.
Human Genetics: Human genetics is the scientific study of how traits, diseases, and characteristics are inherited and expressed in humans. It explores genes, DNA structure, mutations, and patterns of inheritance to understand human diversity and genetic disorders. This field supports diagnosis, prevention, and treatment of hereditary conditions.
Molecular Genetics: Molecular genetics is the branch of biology that studies genes at the molecular level, focusing on the structure, function, and regulation of DNA and RNA. It examines how genetic information is encoded, replicated, expressed, and passed on to the next generation. This field helps explain hereditary traits, genetic variations, and molecular mechanisms underlying diseases.
Genomic Medicine: Genomic medicine is the field that uses an individual’s genetic information to guide disease prevention, diagnosis, and treatment. It identifies genetic variations that influence health, enabling personalized medical decisions and targeted therapies for better patient outcomes.
Population Genetics: Population genetics is the study of how gene frequencies change within and between populations over time. It examines genetic variation, evolutionary forces (such as mutation, natural selection, gene flow, and genetic drift), and how these factors shape the genetic structure and evolution of species.
Evolutionary Genetics: Evolutionary genetics is the study of how genetic variation arises, changes, and is inherited within populations over time. It examines the mechanisms of evolution—such as mutation, natural selection, gene flow, and genetic drift—and how these forces shape the genetic makeup of species. This field helps explain adaptation, speciation, and the evolutionary relationships among organisms.
Functional Genomics: Functional genomics is the field of molecular biology that studies how genes and their products (RNA and proteins) function and interact within a cell or organism. It focuses on understanding gene expression, regulation, and biological pathways using high-throughput technologies. The goal is to link genotype to phenotype and uncover how genetic variations influence biological function.
Epigenetics: Epigenetics refers to the study of heritable changes in gene expression that occur without altering the DNA sequence itself. These changes are influenced by mechanisms such as DNA methylation, histone modification, and non-coding RNAs, affecting how genes are turned on or off in response to environmental or developmental factors.
DNA Sequencing: DNA sequencing is the process of determining the precise order of nucleotides (A, T, C, and G) in a DNA molecule. It provides a detailed genetic blueprint that helps identify genes, detect mutations, and understand biological functions.
