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Human Genome Variation : Impact Factor & More
eISSN: 2054-345XpISSN: 2054-345X
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Human Genome Variation Key Metrics
CiteScore 
2.8
SJR
Q4Genetics
SNIP
0.63
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 months32%
4 to 6 months53%
7 to 9 months9%
Above 9 months6%
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Topics Covered on Human Genome Variation
Genetic variation
Hypertrophic cardiomyopathy
Microcephaly
Exome sequencing
Short stature
Infection rate
Xeroderma pigmentosum
Haplotype
Retinitis pigmentosa
Tuberous sclerosis
Ovarian cancer
Prenatal diagnosis
Arthrogryposis
Duchenne muscular dystrophy
Primary microcephaly
Hypopituitarism
Nucleotide Excision Repair Pathway
Severe phenotype
Pharmacogenomic Variants
Periventricular heterotopia
Human Genome Variation Journal Specifications
Indexed in the following public directories
Web of Science 
Scopus 
DOAJ 
SJR
| Overview | |
| Publisher | SPRINGERNATURE |
| Language | English |
| Frequency | Continuous publication |
| Article Processing Charges | EUR 2490 | USD 2890 | GBP 2190 |
| Publication Time | 13 |
| Editorial Review Process | Anonymous peer review |
| General Details | |
| Language | English |
| Society/Institute/Sponsor | The Japan Society of Human Genetics |
| Frequency | Continuous publication |
| Publication Start Year | 2014 |
| 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-NC-ND |
| OA statement | Visit website |
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Planning to publish in Human Genome Variation ?
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Recently Published Papers in Human Genome Variation
A case of CDKL5 deficiency disorder with a novel intragenic multi-exonic duplication
- 8 Nov 2024
- Human Genome Variation
A mild case of Cockayne syndrome with a novel start-loss variant of ERCC8
- 7 Nov 2024
- Human Genome Variation
Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring system
- 24 Oct 2024
- Human Genome Variation
Detecting adaptive changes in gene copy number distribution accompanying the human out-of-Africa expansion
- 23 Sep 2024
- Human Genome Variation
Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome
- 17 Sep 2024
- Human Genome Variation
Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes
- 30 Aug 2024
- Human Genome Variation
A case of CDKL5 deficiency disorder with a novel intragenic multi-exonic duplication
- 8 Nov 2024
- Human Genome Variation
A mild case of Cockayne syndrome with a novel start-loss variant of ERCC8
- 7 Nov 2024
- Human Genome Variation
Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring system
- 24 Oct 2024
- Human Genome Variation
Detecting adaptive changes in gene copy number distribution accompanying the human out-of-Africa expansion
- 23 Sep 2024
- Human Genome Variation
Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome
- 17 Sep 2024
- Human Genome Variation
Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes
- 30 Aug 2024
- Human Genome Variation
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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 Genome Variation
How long has Human Genome Variation been actively publishing? 
Human Genome Variation has been in operation since 2014 till date.
What is the publishing frequency of Human Genome Variation?
Human Genome Variation published with a Continuous publication frequency.
How many articles did Human Genome Variation publish last year?
In 2023, Human Genome Variation publsihed 30 articles.
What is the eISSN & pISSN for Human Genome Variation?
For Human Genome Variation, eISSN is 2054-345X and pISSN is 2054-345X.
What is Citescore for Human Genome Variation?
Citescore for Human Genome Variation is 2.8.
What is SNIP score for Human Genome Variation?
SNIP score for Human Genome Variation is 0.63.
What is the SJR for Human Genome Variation?
SJR for Human Genome Variation is Q4.
Who is the publisher of Human Genome Variation?
SPRINGERNATURE is the publisher of Human Genome Variation.
