Human Genome Variation

eISSN: 2054-345XpISSN: 2054-345X
JournalOpen Access

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Key Metrics

CiteScore
2.8
SJR
Q4Genetics
SNIP
0.63
3
Time to Publish
time-to-publish View Chart
4  Mo

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
  • Website URL
Publication Details
Editorial Review Detail
Information for authors
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Time to Publish
Time to publish distribution
Articles published in year 2022
Time to publish index
Months% Papers published
0-3 27%
4-6 55%
7-9 9%
>9 9%

Topics Covered

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

Recently Published Papers

Year-wise Publication

FAQs

Since when has Human Genome Variation been publishing? Faqs

The Human Genome Variation has been publishing since 2014 till date.

How frequently is the Human Genome Variation published? Faqs

Human Genome Variation is published Continuous publication.

Who is the publisher of Human Genome Variation? Faqs

The publisher of Human Genome Variation is SPRINGERNATURE.

How can I view the journal metrics of Human Genome Variation on editage? Faqs

For the Human Genome Variation metrics, please refer to the section above on the page.

What is the eISSN and pISSN number of Human Genome Variation? Faqs

The eISSN number is 2054-345X and pISSN number is 2054-345X for Human Genome Variation.

What is the focus of this journal? Faqs

The journal covers a wide range of topics inlcuding 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.

Why is it important to find the right journal for my research? Faqs

Choosing the right journal ensures that your research reaches the most relevant audience, thereby maximizing its scholarly impact and contribution to the field.

Can the choice of journal affect my academic career? Faqs

Absolutely. Publishing in reputable journals can enhance your academic profile, making you more competitive for grants, tenure, and other professional opportunities.

Is it advisable to target high-impact journals only? Faqs

While high-impact journals offer greater visibility, they are often highly competitive. It's essential to balance the journal's impact factor with the likelihood of your work being accepted.