Key Metrics
CiteScore 

3.3
Impact Factor 

< 5
SJR 

Q4Genetics

SNIP 

0.79
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Topics Covered on Molecular genetics & genomic medicine
Molecular genetics & genomic medicine Journal Specifications
Indexed in the following public directories
Web of Science
Scopus
DOAJ
SJR
| Overview | |
| Publisher | WILEY |
| Language | English |
| Frequency | Monthly |
| Article Processing Charges | EUR 2200 | GBP 1950 | USD 2574 |
| Publication Time | 14 |
| Editorial Review Process | Anonymous peer review |
| General Details | |
| Language | English |
| Frequency | Monthly |
| Publication Start Year | 2013 |
| Publisher URL | Visit website |
| Website URL | Visit website |
| Publication Details | |
| Editorial Review Detail | |
| Information for authors | |
| Author instructions | Visit website |
| Copyright Details | Visit website |
| Deposit Policy | Sherpa/Romeo |
| License type | CC BY, CC BY-NC, CC BY-NC-ND |
| OA statement | Visit website |
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Recently Published Papers in Molecular genetics & genomic medicine
Title not available
- 1 May 2026
- Molecular Genetics & Genomic Medicine
Novel <scp>LAMA1</scp> Mutations in a Pedigree With Poretti‐Boltshauser Syndrome: Implications for Hypomyelination
- 27 Apr 2026
- Molecular Genetics & Genomic Medicine
Issue Information
- 23 Apr 2026
- Molecular Genetics & Genomic Medicine
Clinical and Neurodevelopmental Course in a Case of EFNB1-Related Craniofrontonasal Syndrome With Unrepaired Craniosynostosis.
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- Molecular genetics & genomic medicine
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Prenatal Diagnosis of Autosomal Recessive Primary Microcephaly Type 2 Caused by Compound Heterozygous WDR62 Variants in a Family With Two Recurrent Cases.
- 1 Apr 2026
- Molecular genetics & genomic medicine
Title not available
- 1 May 2026
- Molecular Genetics & Genomic Medicine
Novel <scp>LAMA1</scp> Mutations in a Pedigree With Poretti‐Boltshauser Syndrome: Implications for Hypomyelination
- 27 Apr 2026
- Molecular Genetics & Genomic Medicine
Issue Information
- 23 Apr 2026
- Molecular Genetics & Genomic Medicine
Clinical and Neurodevelopmental Course in a Case of EFNB1-Related Craniofrontonasal Syndrome With Unrepaired Craniosynostosis.
- 23 Apr 2026
- Molecular genetics & genomic medicine
A Genetic Landscape of Euploid Miscarriages From Couples With Recurrent Pregnancy Loss Through Whole Exome Sequencing.
- 1 Apr 2026
- Molecular genetics & genomic medicine
Prenatal Diagnosis of Autosomal Recessive Primary Microcephaly Type 2 Caused by Compound Heterozygous WDR62 Variants in a Family With Two Recurrent Cases.
- 1 Apr 2026
- Molecular genetics & genomic medicine