Journal of Hereditary Diseases

Aims and Scope

Journal of Hereditary Diseases (JHD) is a peer-reviewed, open-access journal dedicated to advancing scientific knowledge in the field of hereditary disorders. JHD serves as a global platform for researchers, clinicians, and academicians to share their findings on the genetic and environmental factors influencing heritable medical conditions. 

Scope & Focus Areas:

JHD publishes high-quality research reports, reviews, editorials, commentaries, and case studies covering diverse aspects of hereditary diseases, including:

• Genetic and Molecular Mechanisms: Insights into gene mutations, inheritance patterns, epigenetic regulation, and genome editing technologies.
• Pathogenesis and Clinical Manifestations: Understanding disease progression, phenotypic variations, and clinical management of inherited disorders.
• Diagnosis and Therapeutic Strategies: Advancements in genetic screening, biomarker identification, personalized medicine, and emerging gene therapies.
• Epidemiology and Prevention: Investigations into disease prevalence, risk assessment, and preventive healthcare strategies.
• Public Health and Policy: Ethical, legal, and social implications of hereditary diseases, healthcare policies, and community-based interventions.
   

The Journal of Hereditary Diseases is now accepting submissions that focus on the application of artificial intelligence (AI) in the study of hereditary and genetic disorders. Few keywords were outlined that belongs to the journal scope, not confined to it. If you have any queries, do not hesitate to contact us at [email protected]

• Cystic fibrosis
• Epigenetics
• Genealogy
• Genetic drift
• Gene therapy
• Heredity
• Cytogenetics
• Population genetics
• Hereditary diseases
• Genetic disorders
• Inherited conditions
• Mendelian disorders
• Chromosomal abnormalities
• Genetic mutations
• Genetic testing
• Genetic counseling
• Genetic diagnosis
• Genetic screening
• Genetic engineering
• Genetic regulation
• Thalassemia
• Gene expression
• Genetic inheritance
• Genomic medicine
• Pharmacogenomics
• Marfan syndrome
• Metabolic disorders
• Cardiovascular genetics
• Neurogenetics
• Rare genetic diseases
• Williams syndrome
• Mitochondrial disorders
• Lysosomal storage diseases
• Hemoglobinopathies
• Hereditary cancer syndromes
• Genetic immunodeficiencies
• Genetic hearing loss
• Genetic ophthalmic diseases
• Muscular dystrophy
• Genetic skin disorders
• Genetic renal disorders
• Genetic respiratory disorders
• Genetic muscular disorders
• Genetic endocrine disorders
• Genetic metabolic bone diseases
• Genetic liver diseases
• Genetic dental disorders
• Genetic connective tissue disorders
• Genetic developmental disorders
• Genetic neuropsychiatric disorders
• Genetic disorders in children
• Genetic disorders in adults
• Genetic epidemiology
• Genetics of aging
• Genetics of longevity
• Genetics of behavior
• Genetic variability
• Genetic diversity
• Gene editing
• Personalized medicine