About the Journal of Hereditary Diseases
Advancing genetic medicine through peer-reviewed research on inherited disorders, molecular mechanisms, and translational genomics — connecting clinicians, geneticists, and researchers worldwide.
JHD welcomes manuscripts that illuminate the genetic, molecular, and clinical dimensions of hereditary diseases. Our scope encompasses mechanistic discoveries, diagnostic innovations, therapeutic strategies, and population-level studies that enhance understanding of inherited conditions across diverse populations.
Positional cloning, linkage analysis, chromosome mapping, and identification of disease-causing genetic variants.
Whole genome sequencing, exome analysis, variant interpretation, and next-generation sequencing applications in hereditary disease.
Therapeutic gene editing, viral vector delivery, CRISPR applications, RNA therapeutics, and clinical trial outcomes.
Newborn screening, carrier detection, prenatal diagnosis, preimplantation testing, and population screening programs.
Pathophysiology of genetic mutations, protein dysfunction, cellular pathways, and genotype-phenotype correlations.
Population genetics, genetic diversity, gene flow, evolutionary conservation, and phylogenetic analysis of disease alleles.
Additional topics include genetic codon function, gene chip technology applications, pharmacogenomics of inherited disorders, epigenetic modifications in hereditary disease, mitochondrial genetics, chromosomal abnormalities, and translational bioinformatics. For comprehensive scope details, consult our Aims & Scope page.
JHD combines rigorous peer review with efficient editorial workflows to support genetic researchers navigating complex publication landscapes. Our editorial board comprises internationally recognized experts in clinical genetics, molecular biology, genomic medicine, and genetic counseling who curate submissions for scientific integrity, clinical relevance, and methodological rigor.
- Rigorous Peer Review: Expert evaluation by specialists in genetic medicine, molecular genetics, and clinical genomics ensures high scientific standards.
- Global Visibility: Indexed across genetic databases, biomedical repositories, and academic search platforms to maximize research impact.
- Interdisciplinary Integration: Bridging basic genetics, clinical medicine, bioinformatics, and public health genetics.
- International Reach: Authors from 50+ countries access our platform to share findings with the global genetics community.
- Open Access Equity: Creative Commons licensing enables unrestricted use by clinicians, educators, patients, and policymakers.
- Rapid Publication: Streamlined editorial processes prioritize timely dissemination without compromising quality.
Transparency Commitment: JHD adheres to COPE (Committee on Publication Ethics) guidelines and maintains strict policies on data sharing, conflict of interest disclosure, and research integrity. Our editorial framework protects authors, reviewers, and readers through clear governance at every publication stage.
Distinguished Editorial Board
Expert-Led CurationThe JHD Editorial Board comprises leading experts in genetics, molecular biology, biochemistry, and clinical medicine. Board members bring extensive experience across genetic research methodologies and are committed to upholding the highest international standards in research publishing. They collaborate to ensure each published article delivers valuable insights into hereditary disease mechanisms, diagnostics, and therapeutics.
Our editorial team conducts thorough peer review to validate methodological rigor, reproducibility, and translational significance. This collaborative approach ensures JHD publications meet benchmarks for clinical application, genetic counseling practice, and policy development. Explore the full board composition and expertise areas at our Editorial Board page.
JHD streamlines manuscript submission and review to respect researchers' time while maintaining rigorous evaluation. Authors benefit from transparent communication, constructive feedback, and rapid decision timelines throughout the publication journey.
Submission Pathways: Manuscripts can be submitted via email, our online submission form, or the Manuscript Zone portal. Before submission, authors should review our comprehensive Instructions for Authors for formatting requirements, ethical guidelines, and reporting standards compliance.
All submissions undergo similarity screening, methodological assessment, and ethical compliance verification before peer review assignment. Reviewers provide substantive feedback on study design, genetic analysis methods, statistical approaches, and clinical implications. Editorial decisions outline clear revision expectations and timelines to facilitate efficient manuscript improvement.
Upon completion of peer review, accepted articles are published online in HTML, XML, and PDF formats under a valid Creative Commons Attribution license. Authors retain copyright while granting unrestricted reuse rights, enabling integration into clinical protocols, educational materials, systematic reviews, and policy documents.
Recognizing diverse economic contexts, JHD maintains reasonable and transparent article processing charges to support sustainable open access publishing. Waiver and discount programs support authors from lower-income countries, early-career researchers, and unfunded projects. Contact our editorial office at [email protected] to discuss financial assistance options.
"I was impressed by the swift services of the journal and easy navigation beginning from manuscript submission to galley proof. I would recommend future authors — consider this journal if you are wondering where to publish your scientific work. They are Google Scholar indexed so you do not have to worry if your scientific work won't reach the community of other researchers."
Long Island University
"The positive editorial attitude and cooperation were encouraging and supportive. Moreover, fast response and processing of the manuscript reflect an appreciation of the time factor. The user-friendly submission system allows for up-to-date follow-up. The review process is performed in reasonable time with constructive comments that aim to improve paper quality. Communication between authors and journals in such a way is not common nowadays."
Cairo University
JHD articles are distributed across major genetic databases, biomedical repositories, and academic search platforms to ensure maximum visibility among clinicians, researchers, genetic counselors, and policymakers. Our indexing strategy positions published research for citation growth, clinical uptake, and inclusion in systematic reviews.
Articles are searchable through Google Scholar, institutional repositories, specialized genetics databases, and cross-disciplinary collections. DOI registration via Crossref enables permanent citation tracking and integration into reference management systems. Authors benefit from enhanced discoverability through metadata optimization, structured abstracts, and keyword indexing.
Contact Information: For inquiries regarding scope alignment, submission requirements, peer review processes, or partnership opportunities, please contact our editorial office at [email protected]. Our team is committed to providing responsive, professional support throughout your publishing journey.
