Human Mutation : Impact Factor & More
eISSN: 1098-1004pISSN: 1059-7794
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Key Metrics
CiteScore 
8.6
Impact Factor
< 5
SNIP
1.75
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Topics Covered on Human Mutation
Human Mutation Journal Specifications
Indexed in the following public directories
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Scopus 
SJR
| Overview | |
| Publisher | WILEY-HINDAWI |
| Language | English |
| Frequency | Continuous publication |
| General Details |
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Recently Published Papers in Human Mutation
Integrative Genomic and Functional Analysis Reveals NF1 Loss as a Modifier of DNA Damage and Replication Stress Responses in Ovarian Cancer
- 18 May 2026
- Human Mutation
Decoding the Sphingolipid Landscape of Clear Cell Renal Cell Carcinoma: A Single\u2010Cell\u2010Guided Prognostic Model Built With 101 Machine Learning
- 17 May 2026
- Human Mutation
Secretory Lysosome\u2010Related Gene Signature Defines the Immune Microenvironment and Identifies RGS2 as a Prometastatic Factor in Hepatocellular Carcinoma
- 16 May 2026
- Human Mutation
Novel Variants in the SLC16A2 Gene Associated With Allan\u2013Herndon\u2013Dudley Syndrome in China
- 16 May 2026
- Human Mutation
Cross\u2010Cohort Transcriptomic Integration Identifies IFIT2 as a Translational Diagnostic Biomarker and Functional Driver of Inflammation\u2010Linked Tubular Injury in Chronic Kidney Disease
- 16 May 2026
- Human Mutation
MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level
- 14 May 2026
- Human Mutation
Integrative Genomic and Functional Analysis Reveals NF1 Loss as a Modifier of DNA Damage and Replication Stress Responses in Ovarian Cancer
- 18 May 2026
- Human Mutation
Decoding the Sphingolipid Landscape of Clear Cell Renal Cell Carcinoma: A Single\u2010Cell\u2010Guided Prognostic Model Built With 101 Machine Learning
- 17 May 2026
- Human Mutation
Secretory Lysosome\u2010Related Gene Signature Defines the Immune Microenvironment and Identifies RGS2 as a Prometastatic Factor in Hepatocellular Carcinoma
- 16 May 2026
- Human Mutation
Novel Variants in the SLC16A2 Gene Associated With Allan\u2013Herndon\u2013Dudley Syndrome in China
- 16 May 2026
- Human Mutation
Cross\u2010Cohort Transcriptomic Integration Identifies IFIT2 as a Translational Diagnostic Biomarker and Functional Driver of Inflammation\u2010Linked Tubular Injury in Chronic Kidney Disease
- 16 May 2026
- Human Mutation
MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level
- 14 May 2026
- Human Mutation
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