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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
View Chart Mo
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
| Overview | |
| Publisher | WILEY-HINDAWI |
| Language | English |
| Frequency | Continuous publication |
| General Details |
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Time to Publish
% of papers by time taken from submission to publication
0 to 3 months6%
4 to 6 months58%
7 to 9 months23%
Above 9 months13%
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Recently Published Papers in Human Mutation
RNA Panel Sequencing Is an Effective Tool to Help Classify Splice Variants for Clinical Oncogenetic Diagnosis
- 2 Apr 2024
- Human Mutation
Genome Sequencing of Idiopathic Speech Delay
- 28 Mar 2024
- Human Mutation
Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency
- 25 Mar 2024
- Human Mutation
Estimation of the Age of the Kashubian-Specific Pathogenic NPHS2 Variant Responsible for Hereditary Steroid-Resistant Nephrotic Syndrome Points to Its Recent Local Origin
- 21 Mar 2024
- Human Mutation
Whole-Exome Sequencing Analysis Identifies Risk Genes in Atlantoaxial Dislocation Patients with Sandwich Fusion
- 12 Mar 2024
- Human Mutation
Identification of a Novel NLRP12 Frameshift Mutation (Val730Glyfs<math xmlns="http://www.w3.org/1998/Math/MathML" id="M1"><msup><mrow /><mrow><mo>∗</mo></mrow></msup></math>41) by Whole-Exome Sequencing in Patients with Crohn’s Disease
- 23 Feb 2024
- Human Mutation
RNA Panel Sequencing Is an Effective Tool to Help Classify Splice Variants for Clinical Oncogenetic Diagnosis
- 2 Apr 2024
- Human Mutation
Genome Sequencing of Idiopathic Speech Delay
- 28 Mar 2024
- Human Mutation
Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency
- 25 Mar 2024
- Human Mutation
Estimation of the Age of the Kashubian-Specific Pathogenic NPHS2 Variant Responsible for Hereditary Steroid-Resistant Nephrotic Syndrome Points to Its Recent Local Origin
- 21 Mar 2024
- Human Mutation
Whole-Exome Sequencing Analysis Identifies Risk Genes in Atlantoaxial Dislocation Patients with Sandwich Fusion
- 12 Mar 2024
- Human Mutation
Identification of a Novel NLRP12 Frameshift Mutation (Val730Glyfs<math xmlns="http://www.w3.org/1998/Math/MathML" id="M1"><msup><mrow /><mrow><mo>∗</mo></mrow></msup></math>41) by Whole-Exome Sequencing in Patients with Crohn’s Disease
- 23 Feb 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
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 3 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.
