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
Maternal age and the parental origin of trisomy 21 in Libyan individuals with Down syndrome: a preliminary familial D21S11 STR study
- 24 Oct 2026
- Human Genome Variation
A novel GLDC p.(Cys300Arg) variant in neonatal nonketotic hyperglycinemia
- 23 Sep 2026
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Benign enlargement of the subarachnoid space with transient intracranial hypertension in Marfan syndrome carrying a novel FBN1 variant
- 18 Sep 2026
- Human Genome Variation
Novel ACVRL1 variant in a family with hereditary hemorrhagic telangiectasia
- 2 Sep 2026
- Human Genome Variation
Varporter: a software platform for comprehensive genomic profiling (CGP) in cancer.
- 24 Jul 2026
- Human genome variation
Functional evidence for SCN8A splice-donor variant c.4419+1\u2009A\u2009>\u2009G causing loss of function
- 29 Jun 2026
- Human Genome Variation
Maternal age and the parental origin of trisomy 21 in Libyan individuals with Down syndrome: a preliminary familial D21S11 STR study
- 24 Oct 2026
- Human Genome Variation
A novel GLDC p.(Cys300Arg) variant in neonatal nonketotic hyperglycinemia
- 23 Sep 2026
- Human Genome Variation
Benign enlargement of the subarachnoid space with transient intracranial hypertension in Marfan syndrome carrying a novel FBN1 variant
- 18 Sep 2026
- Human Genome Variation
Novel ACVRL1 variant in a family with hereditary hemorrhagic telangiectasia
- 2 Sep 2026
- Human Genome Variation
Varporter: a software platform for comprehensive genomic profiling (CGP) in cancer.
- 24 Jul 2026
- Human genome variation
Functional evidence for SCN8A splice-donor variant c.4419+1\u2009A\u2009>\u2009G causing loss of function
- 29 Jun 2026
- Human Genome Variation
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