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Genetic Predisposition and Clinical Presentations of Hereditary Cancer

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Epidemiology and Prevention".

Deadline for manuscript submissions: closed (30 November 2023) | Viewed by 61

Special Issue Editors


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Guest Editor
MGZ - Medical Genetics Center and Arbeitsgruppe Erbliche Gastrointestinale Tumore, Medizinische Klinik und Poliklinik IV – Campus Innenstadt, Klinikum der Universität München, 80335 Munich, Germany
Interests: hereditary gastrointestinal tumor syndromes

E-Mail Website
Guest Editor
MGZ - Medical Genetics Center and Arbeitsgruppe Erbliche Gastrointestinale Tumore, Medizinische Klinik und Poliklinik IV – Campus Innenstadt, Klinikum der Universität München, 80335 Munich, Germany
Interests: hereditary gastrointestinal tumor syndromes

Special Issue Information

Dear Colleagues,

Genetic tumor risk syndromes (GENTURIS) affect at least 1 % of all people. Therefore, a relevant number of tumors each year occur in the context of a GENTURIS, of which many patients are not aware before their tumor diagnosis. As risk-adapted surveillance in these patients might lead to earlier detection or even prevention of these tumors and there are more and more specific treatment options emerging, efforts should be undertaken to enhance detection of GENTURIS patients.

In this respect, we are pleased to invite you to contribute to a Special Issue on “Genetic Predisposition and Clinical Presentations of Hereditary Cancer”. This project will give an overview of the most relevant GENTURIS. Therefore, diagnosis, surveillance and treatment of hereditary colorectal and breast cancer will be covered as well as other more rare GENTURIS. The Special Issue aims to spread knowledge and raise awareness of GENTURIS and the special needs of these patients. Consequently, original research articles and reviews are welcome. Research areas may include (but are not limited to) the following: Lynch Syndrome; somatic mosaics; gastrointestinal polyposis syndromes; hereditary gastric cancer; PTEN hamartoma tumor syndrome; hereditary breast cancer; hereditary endocrine tumors; childhood cancers and hereditary tumor predisposition; hereditary hematological neoplasias; heritability of cancer.

We look forward to receiving your contributions.

Prof. Dr. Elke Holinski-Feder
Dr. Verena Steinke-Lange
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cancers is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • hereditary tumor predisposition
  • genetic tumor risk syndromes (GENTURIS)
  • colorectal cancer
  • breast cancer
  • somatic mosaics
  • childhood cancer

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Published Papers

There is no accepted submissions to this special issue at this moment.
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