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    Human Genome Variation

    Human Genome Variation is Scopus-indexed (Q4, CiteScore 2.3), WoS ESCI, DOAJ. Published by Springer Nature.

    Checked against the index lists dated 4 October 2026.

    ISSN 2054-345XVerify ISSN ↗

    Publisher: Springer Nature

    Scopus · Q4WoS · ESCIOpen Access
    2.3
    CiteScore 2025
    Scopus
    Q4
    Best quartile
    rank 347 of 448 · 22nd pctile
    3
    Indexed in
    major indexes

    Cost to publish: Checking DOAJ for article charges…

    ScopusElsevier Scopus
    Status
    Active
    Coverage
    2014–present
    Source type
    Journal
    Open access
    Yes
    CiteScore
    2.3
    SJR · SCImago
    0.535
    Q3 SJR quartile
    H-index
    28
    Best quartile
    Q4 · 22nd pctile
    Subject areaRankPctileQ
    Biochemistry347 / 44822ndQ4
    Genetics280 / 35721stQ4
    Molecular Biology339 / 41418thQ4
    View this source on Scopus.com
    Web of ScienceClarivate (SCIE/SSCI/AHCI/ESCI)
    Collections
    ESCI
    Categories
    Genetics & Heredity
    View this source on Web of Science Check JIF in JCR
    DOAJDirectory of Open Access Journals (live)
    Listed in DOAJ
    Open accessFully open access, peer reviewed

    Not listed in: ABDC, ABS / AJG, FT50, UT Dallas, ONOS (subscription), ONOS (APC covered)

    Quick answers

    Is Human Genome Variation indexed in Scopus?

    Yes — actively indexed in Scopus, coverage 2014–present, best quartile Q4, CiteScore 2.3.

    What quartile is Human Genome Variation in Scopus?

    Human Genome Variation is Q4 in Biochemistry (rank 347 of 448), Q4 in Genetics (rank 280 of 357) and Q4 in Molecular Biology (rank 339 of 414), by CiteScore 2025.

    What is the impact factor of Human Genome Variation?

    Human Genome Variation is indexed in the Emerging Sources Citation Index, so it may have a Journal Impact Factor in Clarivate's Journal Citation Reports. JCR is paid, so check it for the current value. The closest free measure is its Scopus CiteScore 2.3, which places it in quartile Q4 at the 22nd percentile of its subject. Its SCImago Journal Rank (SJR, a free Scopus-based metric) is 0.535, quartile Q3, with an H-index of 28.

    How much does it cost to publish in Human Genome Variation?

    The publisher lists an article processing charge of about US$3,190 for open access (source: OpenAlex). Many journals also publish by the subscription route at no cost to the author, so confirm on the journal's own website.

    Who publishes Human Genome Variation and what is its ISSN?

    Human Genome Variation is published by Springer Nature. Its ISSN is 2054-345X.

    Is Human Genome Variation in Web of Science?

    Yes — indexed in the Emerging Sources Citation Index.

    Is Human Genome Variation open access?

    Yes — it is an open-access journal, listed in DOAJ.

    How well cited is Human Genome Variation? — open metrics via OpenAlex

    Human Genome Variation has an h-index of 33 and a 2-year mean of 1.81 citations per paper (OpenAlex). Its Scopus CiteScore is 2.3, quartile Q4. On 2-year citations it ranks #285 of 442 Scopus journals in Biochemistry.

    33
    h-index
    1.81
    2-yr mean citations
    186
    i10-index
    536
    works indexed
    5,721
    total citations
    Publication fee · open access list price, US$
    US$3,190
    05001,0002,0003,000+
    2-yr mean citations, among Scopus journals in the same subject
    #285 of 442 Bottom 36% Biochemistry
    #227 of 353 Bottom 36% Genetics
    #286 of 411 Bottom 31% Molecular Biology
    Papers published per year
    0501002017: 48 papers4820172018: 50 papers5020182019: 56 papers5620192020: 46 papers4620202021: 46 papers4620212022: 49 papers4920222023: 30 papers3020232024: 47 papers4720242025: 29 papers2920252026: 25 papers so far252026*

    Human Genome Variation published 29 papers in 2025; its busiest recent year was 2019 with 56. 2026* is the year so far.

    Main topics
    Genomics and Rare DiseasesGenomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental DisordersConnective tissue disorders research

    h-index, i10-index and 2-year mean citedness are open, licence-clear metrics from OpenAlex — not a proprietary impact factor. The subject rank counts only journals that OpenAlex has a figure for; it is not a Scopus or Clarivate ranking. Updated 2026-10-14.

    Who publishes in Human Genome Variation? — latest 100 articles, 2024–2026

    In its latest 100 research articles (2024–2026), authors are most often from Japan (76.5%), Iran (3%) and India (2%). More than half of recent authorship comes from one country.

    Author countriesJapanJapan76.5%IranIran3%IndiaIndia2%GermanyGermany1.8%MalaysiaMalaysia1.5%BrazilBrazil1.3% Most frequent institutions (papers)National Center For Child Health and DevelopmentNational Center For Child Healt…9Yokohama City UniversityYokohama City University8Keio UniversityKeio University6Nagoya UniversityNagoya University5Okayama UniversityOkayama University5

    Countries are counted fractionally, so a paper by authors from two countries counts half to each.

    Are there integrity warnings for Human Genome Variation? — indicators, not proof of misconduct

    Scopus status: Active. No retracted papers are recorded. The Problematic Paper Screener flags none of its papers. These are indicators to check, not findings against the journal.

    • Scopus statusActive
    • Retracted papers None recorded
    • Problematic Paper Screener flags None flagged
    • Author concentration76.5% of recent authorship from Japan

    Retractions from OpenAlex; flags from the Problematic Paper Screener (Cabanac, Labbé & Magazinov, CC BY), 2026-09-21 export. A flag marks a paper for a closer look; it is not a finding against the journal.

    Official sources & links

    Journal website ↗ Scopus source ↗ Web of Science ↗ DOAJ ↗ ISSN Portal · 2054-345X ↗

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