Publications Overview

The reference centres (RC) that comprise the Endo-ERN network are actively involved in rare disease research.

On an annual basis, as part of the Continuous Monitoring (CM) programme, Endo-ERN members report their rare disease publications that involve at least 1 other Endo-ERN member.

This information is now available in a searchable database which will become a comprehensive resource for endocrine clinicians and researchers with an interest in rare disease, particularly those just starting their career.

Before you submit a publication:  

To avoid duplicate entries and delays, please note the following before starting a submission:

  • One submission per publication:
    The database automatically blocks duplicate records. If several authors attempt to submit the same publication, only the first submission will be accepted.
    Please agree in advance who will make the submission on behalf of all authors.
  • Institution names:
    You will be asked to select each author’s institution from a dropdown list.
    Make sure you know the exact institution names as they appear in the system for all co-authors before you begin.
  • ORPHAcode selection:
    Each publication must be linked to the correct ORPHAcode.
    Authors should agree beforehand on the appropriate ORPHAcode(s) to use for the publication.

Taking a few minutes to coordinate with your co-authors in advance will help ensure a smooth and successful submission.  

Endo-ERN has also curated publications for Rare Disease Day (RDD) that showcases member activity. Find previous issues here.

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