Journal of Clinical and Experimental Genetics

About

About the Journal

Journal of Clinical and Experimental Genetics (JCEG) is an open access, peer reviewed multidisciplinary refereed journal devoted to the rapid publication of fundamental advances and innovative research works in the field of Clinical and Experimental genetics by making it freely accessible by various researchers and academicians.

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

Clinical application of whole-exome sequencing across clinical indications

We report the diagnostic yield of whole-exome sequencing (WES) in 3,040 consecutive cases at a single clinical laboratory.

An epigenomic signature of postprandial hyperglycemia in peripheral blood leukocytes

Postprandial hyperglycemia is known to be one of the earliest signs of abnormal glucose homeostasis associated with type 2 diabetes.

Clinical, genetics and bioinformatics characterization of a campomelic dysplasia case report

Campomelic dysplasia is a rare disorder characterized by skeletal and extraskeletal defects. Up to two-thirds of affected XY individuals have a gradation of genital defects or may develop as phenotypic females.

Epigenetic inactivation of the extracellular matrix metallopeptidase ADAMTS19 gene and the metastatic spread in colorectal cancer

ADAMTS19 encodes a member of the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin motifs) protein family with emerging roles in carcinogenesis and metastasis.

The Rho GTPase Family Genes in Bivalvia Genomes: Sequence, Evolution and Expression Analysis

Rho GTPases are important members of the Ras superfamily, which represents the largest signaling protein family in eukaryotes, and function as key molecular switches.