Human Genome Variation

SJR Rank #11,143H-index: 28SJR: 0.535Best quartile: Q3Open AccessAPC: US$3,190Listed in DOAJ
Journal website: aims, scope and author guidelines
Publisher

Springer Nature

Country

United Kingdom

Type

journal

SJR by Edition

2022202500.150.30.450.6

Subject Categories

  • BiochemistryQ3
  • GeneticsQ3
  • Molecular BiologyQ3

Areas: Biochemistry, Genetics and Molecular Biology

Most published research topics

Genomics and Rare DiseasesGenomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental DisordersConnective tissue disorders researchRNA modifications and cancerRNA regulation and diseaseCongenital heart defects researchCell Adhesion Molecules ResearchRNA Research and SplicingMetabolism and Genetic Disorders

Source: OpenAlex

Publication Statistics

2025 Docs3-Year DocsCitable Docs03570105140

Documents per Year

20222025015304560

Detailed Information

ISSN

2054-345X

SJR Best Quartile

Q3

Region

Western Europe

Citations per Document (2 years)

1.37

References per Document

18.14

Coverage

2014-2026

Scope

Human Genome Variation is an online-only, full open access journal that contains articles and reports about variation and variability in human genomes and the consequences, implications and future impacts for the study of human genomics. An important and innovative feature of the journal is the Data Report article; these are short reports about human genome variation and variability which describe disease-causing variation and/or their frequencies. In addition, Data Reports can describe and analyse human multifactorial disease associated variations and/or their frequencies. A further feature of Human Genome Variation is a curated database of the underlying data from Data Reports, which will grow into an important resource for the genomics community. Human Genome Variation also publishes Articles and Reviews on the relevant topics in human genome studies. Full Articles is accompanied by a professionally written Editorial Summary. The intended audience for Human Genome Variation is researchers, scientists, clinicians, genetic counsellors and those interested in human genomics, from all sectors and from around the world.

Metrics from SCImago Journal Rank 2025. View on SCImago