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Impact Factor 3.517 | CiteScore 3.60
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Scope
The acquisition of somatic genetic aberrations is central to the development of cancer, along with the constitutional genetic background of each patient in their cancer risk and response to therapy. Current technologies provide ever more powerful approaches to study and validate these highly complex phenomena. The Cancer Genetics specialty section will facilitate the publication of high-quality original research and review articles pertaining to the genetic, genomic and molecular aspects of cancer, and technical advances that facilitate progress in this field.
Focused primarily on molecular genetic aberrations driving malignant processes in human cancers, the scope of submissions will include investigations in the following areas:
- Basic and translational studies reporting large-scale genomic and transcriptomic data (e.g. gene expression, copy number, sequencing, DNA polymorphism, and epigenetics) and studies employing classical and molecular cytogenetic techniques.
- Advances in bioinformatics, statistical, and systems approaches to enable novel biological and clinical interpretation of large-scale datasets.
- Studies demonstrating a correlation of genetic changes with pathology and clinical presentation.
- Genetics, genomics and RNA-based biomarker development.
- Whole genome studies and focused studies of individual genes contributing to cancer molecular pathways.
- New rationales for bringing molecular genetic findings to the clinical oncology space.
Submissions not in scope for this specialty include:
- Those consisting solely of bioinformatic investigation of publicly available genomic / transcriptomic data without experimental or in situ validation to support conclusions.
- Those focused on proteomic and metabolomic investigation.
Indexed in: PubMed, PubMed Central, Scopus, Google Scholar, DOAJ, CrossRef, Chemical Abstracts Service (CAS), EMBASE, AGRICOLA, Semantic Scholar, Ulrich's Periodicals Directory, Science Citation Index Expanded, BIOSIS Citation Index, Biological Abstracts, CLOCKSS, EBSCO, OpenAIRE, Zetoc, Mastermind
PMCID: all published articles receive a PMCID
Cancer Genetics welcomes submissions of the following article types: Clinical Trial, Correction, Editorial, Hypothesis and Theory, Methods, Mini Review, Opinion, Original Research, Perspective, Review, Specialty Grand Challenge, Systematic Review and Technology and Code.
All manuscripts must be submitted directly to the section Cancer Genetics, where they are peer-reviewed by the Associate and Review Editors of the specialty section.
Articles published in the section Cancer Genetics will benefit from the Frontiers impact and tiering system after online publication. Authors of published original research with the highest impact, as judged democratically by the readers, will be invited by the Chief Editor to write a Frontiers Focused Review - a tier-climbing article. This is referred to as "democratic tiering". The author selection is based on article impact analytics of original research published in all Frontiers specialty journals and sections. Focused Reviews are centered on the original discovery, place it into a broader context, and aim to address the wider community across all of Genetics and Oncology.
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Contact Editorial Office
Avenue du Tribunal Fédéral 34
CH – 1005 Lausanne
Switzerland
Tel +41(0)21 510 17 40
Fax +41 (0)21 510 17 01
For all queries regarding manuscripts in Review and potential conflicts of interest, please contact genetics.editorial.office@frontiersin.org
For queries regarding Research Topics, Editorial Board applications, and journal development, please contact genetics@frontiersin.org
Tel +41(0)21 510 17 10
Fax +41 (0)21 510 17 01
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