Human Genome Variation : Impact Factor & More
eISSN: 2054-345XpISSN: 2054-345X
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Key Metrics
CiteScore 
2.8
SJR
Q4Genetics
SNIP
0.63
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Topics Covered on Human Genome Variation
Human Genome Variation Journal Specifications
Indexed in the following public directories
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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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Recently Published Papers in Human Genome Variation
DNA methylation data from Japanese patients with Rubinstein–Taybi syndrome
- 28 Nov 2025
- Human Genome Variation
A novel PKD1 variant in a patient with very-early-onset ADPKD
- 22 Nov 2025
- Human Genome Variation
Fontaine progeroid syndrome with neonatal mitochondrial disease.
- 21 Nov 2025
- Human genome variation
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani family.
- 18 Nov 2025
- Human genome variation
Biallelic CPAMD8 variants in a patient with ectopia lentis associated with extraocular systemic features reminiscent of Marfan syndrome
- 27 Oct 2025
- Human Genome Variation
Biallelic MINAR2 variant is associated with nonsyndromic severe to profound sensorineural hearing loss
- 23 Oct 2025
- Human Genome Variation
DNA methylation data from Japanese patients with Rubinstein–Taybi syndrome
- 28 Nov 2025
- Human Genome Variation
A novel PKD1 variant in a patient with very-early-onset ADPKD
- 22 Nov 2025
- Human Genome Variation
Fontaine progeroid syndrome with neonatal mitochondrial disease.
- 21 Nov 2025
- Human genome variation
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani family.
- 18 Nov 2025
- Human genome variation
Biallelic CPAMD8 variants in a patient with ectopia lentis associated with extraocular systemic features reminiscent of Marfan syndrome
- 27 Oct 2025
- Human Genome Variation
Biallelic MINAR2 variant is associated with nonsyndromic severe to profound sensorineural hearing loss
- 23 Oct 2025
- Human Genome Variation
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