Molecular Cytogenetics

eISSN: 1755-8166pISSN: 1755-8166
JournalOpen Access

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Key Metrics

CiteScore
2.8
Impact Factor
< 5
SJR
Q4Genetics
SNIP
0.73
Time to Publish
time-to-publish View Chart
2  Mo

Journal Specifications

Indexed in the following public directories

  • Web of Science Web of Science
  • Scopus Scopus
  • DOAJ DOAJ
  • SJR SJR
Overview
  • Publisher
    BMC
  • Language
    English
  • Frequency
    Continuous publication
  • Article Processing Charges
    EUR 2590 | USD 3090 | GBP 2190
  • Publication Time
    8
  • Editorial Review Process
    Anonymous peer review
General Details
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 78%
4-6 22%
7-9 0%
>9 0%

Topics Covered

Chromosome
Cohort study
Karyotype
Miscarriage
Bone marrow
Ataxia telangiectasia mutated
Intellectual disability
Satellite DNA
Prenatal diagnosis
Aneuploidy
Fluorescence in situ hybridization
Deletion syndrome
Cardiac defects
5q Deletion
X chromosome
Uniparental disomy
Preimplantation genetic diagnosis
Genome Reference Consortium
Microcephaly
Amniocentesis

Recently Published Papers

Year-wise Publication

FAQs

Since when has Molecular Cytogenetics been publishing? Faqs

The Molecular Cytogenetics has been publishing since 2008 till date.

How frequently is the Molecular Cytogenetics published? Faqs

Molecular Cytogenetics is published Continuous publication.

Who is the publisher of Molecular Cytogenetics? Faqs

The publisher of Molecular Cytogenetics is BMC.

How can I view the journal metrics of Molecular Cytogenetics on editage? Faqs

For the Molecular Cytogenetics metrics, please refer to the section above on the page.

What is the eISSN and pISSN number of Molecular Cytogenetics? Faqs

The eISSN number is 1755-8166 and pISSN number is 1755-8166 for Molecular Cytogenetics.

What is the focus of this journal? Faqs

The journal covers a wide range of topics inlcuding Chromosome, Cohort study, Karyotype, Miscarriage, Bone marrow, Ataxia telangiectasia mutated, Intellectual disability, Satellite DNA, Prenatal diagnosis, Aneuploidy, Fluorescence in situ hybridization, Deletion syndrome, Cardiac defects, 5q Deletion, X chromosome, Uniparental disomy, Preimplantation genetic diagnosis, Genome Reference Consortium, Microcephaly, Amniocentesis.

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.