Academic Journal
Q3Molecular Genetics and Genomic Medicine
About Molecular Genetics and Genomic Medicine
Molecular Genetics and Genomic Medicine is a scholarly journal published by John Wiley and Sons Inc. SCImago 2025 lists it in Q3, with an SJR of 0.596 and H-index of 50.
Coverage: 2013-2026. Research categories: Genetics (Q3); Genetics (clinical) (Q3); Molecular Biology (Q3).
Verified field sources
- Editor(s): Paraminder Dhillon (Editor) — Official source; checked 2026-10-03. Editorial leadership listed under Edited By on the Wiley journal homepage; publisher role retained without assuming Editor-in-Chief.
- Journal Impact Factor: 1.6 — Official source; checked 2026-10-03. Journal Impact Factor and reporting year from Wiley Journal Metrics, distinct from CiteScore and Journal Citation Indicator.
- Impact Factor year: 2025 — Official source; checked 2026-10-03. Journal Impact Factor and reporting year from Wiley Journal Metrics, distinct from CiteScore and Journal Citation Indicator.
Open-access policies and author information
Reported in the official DOAJ public CSV snapshot (2026-09-01), downloaded 2026-10-03. Record updated 2026-03-17. This snapshot does not establish today’s listing status or fee quotation.
Publisher policy links recorded by DOAJ
- Aims and scope ↗
- Editorial board ↗
- Instructions for authors ↗
- Peer-review policy ↗
- Publication fees ↗
- Fee waivers ↗
- Licence terms ↗
- Copyright policy ↗
- Preservation policy ↗
Source: DOAJ journal record. Journal metadata is distributed by DOAJ under CC0. Confirm current fees, tax, eligibility and waiver terms with the publisher.
Source-backed journal facts
Topics in published research
Genomics and Rare Diseases; Genomic variations and chromosomal abnormalities; Connective tissue disorders research; BRCA gene mutations in cancer; Genetics and Neurodevelopmental Disorders; Prenatal Screening and Diagnostics.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
Clinical Epigenomics in Rare Diseases: Interpreting DNA Methylation Episignatures
Himanshu Goel, Shuxiang Goh, Luke Stuart
2026-10 · DOI: 10.1002/mgg3.70319Clinical Practice of Single‐Molecule Real‐Time Sequencing in the Diagnosis of Spinal Muscular Atrophy
Hua Wei, Ya‐Wen Zheng, Ning‐Ke Zhang, Tie‐Li Gao et al.
2026-10 · DOI: 10.1002/mgg3.70314Identification of Variants in Two Families With Congenital Cataract by Whole Exome Sequencing
Yazhou Huang, Xinwei Leng, Jibo Zhang, Xingxin Fang et al.
2026-10 · DOI: 10.1002/mgg3.70313A Novel De Novo MTM1 Insertion Frameshift Variant Causes X‐Linked Myotubular Myopathy in a Chinese Female
Lijun Chen, Yingxiao Bao, Gonglu Liu
2026-10 · DOI: 10.1002/mgg3.70318The Paradox of Progress: Genetic Counselling in a South African Context and the Challenges of Workforce Retention
Samantha Schnell, Katryn Fourie, Elzette Gilfillan, Bianca Rossouw et al.
2026-10 · DOI: 10.1002/mgg3.70310A Heterozygous Variant in the GABBR2 Gene in a Girl With Clinical Classic Rett Syndrome
Jenny Klintenstedt, Peter Baeck, Ingegerd Witt Engerström, Cecilia Gunnarsson et al.
2026-10 · DOI: 10.1002/mgg3.70303Issue Information
2026-10 · DOI: 10.1002/mgg3.70235Novel TCOF1 Frameshift Variant and Phenotypic Heterogeneity in a Chinese Family With Treacher Collins Syndrome
Feiyang Fan, Ying Chen, Tianyu Zhang, Jing Ma et al.
2026-09 · DOI: 10.1002/mgg3.70297Genomic Profiling of Anophthalmia/Microphthalmia‐Associated CNVs Reveals Complex Genotype–Phenotype Correlations and Incomplete Penetrance
Dong Wu, Mengting Zhang, Qian Zhang, Fengyang Wang et al.
2026-09 · DOI: 10.1002/mgg3.70282Monoallelic SH2B1 Variants in Neurodevelopmental Disorders: Phenotypic Expansion and Functional Characterization of Rare Variants
Xin Xu, Gege Yuan, Bixia Zheng, Chunli Wang et al.
2026-09 · DOI: 10.1002/mgg3.70306Clinical Application of Long‐Read Sequencing for FMR1 Gene Mutation Detection in Populations From Shandong, China
Yan Li, Fei Hou, Shan Shan, Yingying Peng et al.
2026-09 · DOI: 10.1002/mgg3.70290Bioinformatics Analysis and Experimental Validation of Key Genes Associated With Hypoxia and Ischemia in Myocardial Infarction
Longsheng Zhang, Ning Liang
2026-09 · DOI: 10.1002/mgg3.70284Pediatric Familial Cerebral Cavernous Malformation Associated With a Novel KRIT1 Initiation‐Region Frameshift Variant
Özlem Yayıcı Köken, Mehpare Sarı Yanartaş, Hande Aygün, Ahmet Cevdet Ceylan et al.
2026-09 · DOI: 10.1002/mgg3.70304Phenotypic and Genotypic Landscape of Sitosterolemia in China: Including a Rare Case With Nephronophthisis
Dan Ding, Hongmei Wu, Fei Zhao, Bixia Zheng et al.
2026-09 · DOI: 10.1002/mgg3.70293Whole‐Exome Sequencing Identifies Novel CPAMD8 Variants in Congenital Cataract and Candidate Variants in Pathologic Myopia
Qiu‐ling Xie, Qiao Wang, Yanan Liu, Teng Huang et al.
2026-09 · DOI: 10.1002/mgg3.70307Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy
Yu Zhang, Shimei Yuan, Yafang Wan, Tian Li et al.
2026-09 · DOI: 10.1002/mgg3.70291Clinical and Genetic Analysis of Pediatric Neurodevelopmental Disorders With Complex Chromosomal Rearrangements in Two Cases
Jiaci Li, Wenxuan Fan, Nan Liu, Shuyue Zhang et al.
2026-09 · DOI: 10.1002/mgg3.70305Analysis of Genetic Factors in a Family With Short Stature
Siqing Zhang, Tian Zuo, Youping Deng, Dongchi Zhao et al.
2026-09 · DOI: 10.1002/mgg3.70288Reviews
Community Reviews
Version History
October 2, 2026 at 9:15 pm
October 2, 2026