Journal of Genetic Mutation Disorders

About

About the Journal

Journal of Genetic Mutation Disorders (JGMD) is an international open access, peer-reviewed journal for the publication of advancements and for dissemination of scientific knowledge on Genetic mutation disorders by covering all aspects like Gene therapy, hereditary genetic disorders, Medical Genetics, Clinical Genetics etc., making it to be visible for various researchers.

Why publish with us

Built for researchers

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Fast peer review

Target first decision within 21 days. Double-blind review by 2-3 field experts.

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Fully open access

All articles CC BY 4.0. No paywalls. Compliant with funder mandates worldwide.

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DOI & indexing

Every article receives a unique DOI. Indexed in PubMed, Google Scholar, CrossRef.

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Rapid publication

Published within 7 days of acceptance. No unnecessary delays in dissemination.

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Global & equitable

Readers in 170+ countries. Waiver program available for authors from developing nations.

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No content limits

No word limits. Multiple article formats: research, reviews, case reports, short communications.

How it works

Simple. Transparent. Streamlined.

Submit

Upload your manuscript via our online portal. Quality check within 48 hours.

Review

Double-blind peer review by 2-3 field experts. Target decision: ~21 days.

Revise

Constructive feedback from reviewers. Dedicated editorial support throughout.

Publish

Published within 7 days. DOI assigned via CrossRef. Globally indexed.

Submit Manuscript →

Highlights

Research Highlights

Prion Diseases

Prion diseases, a group of disorders caused by abnormally shaped proteins called prions, occur in sporadic (Jakob-Creutzfeldt disease), genetic (genetic Jakob-Creutzfeldt disease, Gerstmann-Stra¨ussler-Scheinker syndrome.

Gene-targeting pharmaceuticals for single gene disorders

The concept of orphan drugs for treatment of orphan genetic diseases is perceived enthusiastically at present, and this is leading to research investment on the part of governments, disease-specific foundations, and industry.

Molecular diagnostic experience of whole-exome sequencing in adult patients

Whole-exome sequencing (WES) is increasingly used as a diagnostic tool in medicine, but prior reports focus on predominantly pediatric cohorts with neurologic or developmental disorders.

A novel intranuclear RNA vector system for long-term stem cell modification

Genetically modified stem and progenitor cells have emerged as a promising regenerative platform in the treatment of genetic and degenerative disorders, highlighted by their successful therapeutic use in inherent immunodeficiencies.

Genome-wide Association Studies Identify Genetic Loci Associated with Albuminuria in Diabetes

Elevated concentrations of albumin in the urine, albuminuria, are a hallmark of diabetic kidney disease and associate with increased risk for end-stage renal disease and cardiovascular events.