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Human Mutation : Impact Factor & More
eISSN: 1098-1004pISSN: 1059-7794
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Human Mutation Key Metrics
CiteScore 
8.6
Impact Factor
< 5
SNIP
1.75
Time to Publish
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Time to Publish
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% of papers by time taken from submission to publication
0 to 3 months19%
4 to 6 months45%
7 to 9 months21%
Above 9 months14%
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Topics Covered on Human Mutation
Germline
Hypertrophic cardiomyopathy
Radiation
Intellectual disability
Exome sequencing
Neuroimaging
Allele
Cytochrome c oxidase
Rare disease
Dystrophin
Genome
Endoplasmic reticulum
Retinal degeneration
Hearing loss
Colorectal cancer
Genotype
Exome
Liver dysfunction
Scoliosis
Clinical phenotype
Human Mutation Journal Specifications
Indexed in the following public directories
Web of Science 
Scopus 
SJR
| Overview | |
| Publisher | WILEY-HINDAWI |
| Language | English |
| Frequency | Continuous publication |
| General Details |
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Recently Published Papers in Human Mutation
Treatability of the KMT2-Associated Neurodevelopmental Disorders Using Antisense Oligonucleotide-Based Treatments
- 29 May 2024
- Human Mutation
Characterization and Engineered U1 snRNA Rescue of Splicing Variants in a Turkish Neurodevelopmental Disease Cohort
- 28 May 2024
- Human Mutation
Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1
- 18 May 2024
- Human Mutation
Multiple Sclerosis Polygenic Risk Is Not Enriched in Three Multicase Families in Comparison to Population-Based Cases
- 16 May 2024
- Human Mutation
CAVaLRi: An Algorithm for Rapid Identification of Diagnostic Germline Variation
- 29 Apr 2024
- Human Mutation
The Association of Heterozygous p.R4810K of RNF213 and Long-Term Unfavorable Outcomes after Encephaloduroarteriosynangiosis in Chinese Pediatric Patients with Moyamoya Disease
- 24 Apr 2024
- Human Mutation
Treatability of the KMT2-Associated Neurodevelopmental Disorders Using Antisense Oligonucleotide-Based Treatments
- 29 May 2024
- Human Mutation
Characterization and Engineered U1 snRNA Rescue of Splicing Variants in a Turkish Neurodevelopmental Disease Cohort
- 28 May 2024
- Human Mutation
Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1
- 18 May 2024
- Human Mutation
Multiple Sclerosis Polygenic Risk Is Not Enriched in Three Multicase Families in Comparison to Population-Based Cases
- 16 May 2024
- Human Mutation
CAVaLRi: An Algorithm for Rapid Identification of Diagnostic Germline Variation
- 29 Apr 2024
- Human Mutation
The Association of Heterozygous p.R4810K of RNF213 and Long-Term Unfavorable Outcomes after Encephaloduroarteriosynangiosis in Chinese Pediatric Patients with Moyamoya Disease
- 24 Apr 2024
- Human Mutation
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Compare journals across 7 parameters SJR Ranking, Topics covered, Indexing Database, Publication Review Time, Publication Type, Article Processing Charges & Recently Published papers
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FAQs on Human Mutation
How long has Human Mutation been actively publishing? 
Human Mutation has been in operation since 1992 till date.
What is the publishing frequency of Human Mutation?
Human Mutation published with a Continuous publication frequency.
How many articles did Human Mutation publish last year?
In 2023, Human Mutation publsihed 34 articles.
What is the eISSN & pISSN for Human Mutation?
For Human Mutation, eISSN is 1098-1004 and pISSN is 1059-7794.
What is Citescore for Human Mutation?
Citescore for Human Mutation is 8.6.
What is SNIP score for Human Mutation?
SNIP score for Human Mutation is 1.75.
Who is the publisher of Human Mutation?
WILEY-HINDAWI is the publisher of Human Mutation.
