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
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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
Multi\u2010Level Genomic and Computational Analyses Identify a Novel IFT122 Variant Associated With Cranioectodermal Dysplasia 1 in a Consanguineous Saudi Family
- 17 May 2026
- Molecular Genetics & Genomic Medicine
Title not available
- 1 May 2026
- Molecular Genetics & Genomic Medicine
Homozygous Pathogenic Variant in Elongation Factor-Like 1 (EFL1) as a Causal Factor in Shwachman-Diamond Syndrome 2 in a Palestinian Child, With Distinct Ocular Manifestations.
- 1 May 2026
- Molecular genetics & genomic medicine
Pedigree and Functional Analysis of Two Cryptic OTC Variants Causing Ornithine Transcarbamylase Deficiency in Two Unrelated Chinese Male Patients.
- 1 May 2026
- Molecular genetics & genomic medicine
Identification of a Novel Homozygous SCN1B Splice-Site Variant in a Consanguineous Families With Early-Onset Epilepsy: A Case Series and Review of Literature.
- 1 May 2026
- Molecular genetics & genomic medicine
Identification of a Novel De Novo Heterozygous SEC61A1 Variant in a Patient With Severe Congenital Neutropenia.
- 1 May 2026
- Molecular genetics & genomic medicine
Multi\u2010Level Genomic and Computational Analyses Identify a Novel IFT122 Variant Associated With Cranioectodermal Dysplasia 1 in a Consanguineous Saudi Family
- 17 May 2026
- Molecular Genetics & Genomic Medicine
Title not available
- 1 May 2026
- Molecular Genetics & Genomic Medicine
Homozygous Pathogenic Variant in Elongation Factor-Like 1 (EFL1) as a Causal Factor in Shwachman-Diamond Syndrome 2 in a Palestinian Child, With Distinct Ocular Manifestations.
- 1 May 2026
- Molecular genetics & genomic medicine
Pedigree and Functional Analysis of Two Cryptic OTC Variants Causing Ornithine Transcarbamylase Deficiency in Two Unrelated Chinese Male Patients.
- 1 May 2026
- Molecular genetics & genomic medicine
Identification of a Novel Homozygous SCN1B Splice-Site Variant in a Consanguineous Families With Early-Onset Epilepsy: A Case Series and Review of Literature.
- 1 May 2026
- Molecular genetics & genomic medicine
Identification of a Novel De Novo Heterozygous SEC61A1 Variant in a Patient With Severe Congenital Neutropenia.
- 1 May 2026
- Molecular genetics & genomic medicine