RareBoost Wraps Up 2024 with a Fun-Filled Gathering at IBG
We celebrated the end of 2024 with a wonderful gathering at the IBG. Esteemed guests included DEU Rector and IBG
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Author: Begüm Utz
RareBoost is dedicating January and February to ‘Advanced Technologies in Rare Diseases’
We are excited to announce that RareBoost is dedicating January and February to ‘Advanced Technologies in Rare Diseases’. During these
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9th Rare and Undiagnosed Diseases Patient Advisory Council was held on December 11
The Rare and Undiagnosed Diseases Patient Advisory Council held its 9th meeting on December 11. The meeting began with an
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IBG RareBoost End of the Year Event
We are excited to invite you to IBG RareBoost End of the Year Event, to get together, enjoy some food
Read MoreMedical Genetics Specialist (ERDERA Project, actively recruiting)
Offer Description The European Rare Diseases Research Alliance (ERDERA) (www.erdera.org) is a partnership that aims to improve the health and well-being of
Read MoreProject Manager (ERDERA Project, actively recruiting)
Offer Description We are seeking an experienced and highly qualified Project Manager for the ERDERA project. The European Rare Diseases Research Alliance (ERDERA) (www.erdera.org) is
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Teaching & Training Presentation – Application of iPSCs in Disease Modeling and Therapeutic Development
On Thursday, December 10, 2024, IBG Neurogenomics Laboratory Group Leader Dr. Yavuz Oktay will give a presentation titled ‘Application of iPSCs
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RareBoost concludes “Rare Eye Diseases Awareness Month” with educational events and community engagement
Rare eye diseases are diseases that are seen at a frequency of 1 in 2000 or less in society. Most
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IBG Teaching & Training Presentation – Authorship and Reproducibility of Science
On November 21st 2024, Dr. Gerhard Wingender will give a Teaching & Training presentation discussing ‘Authorship and Reproducibility of Science’.
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RareBoost and IBG-Rare Met with Deniz Yilmaz Atakay, Head of the Rare Diseases Federation
On October 8, 2024, RareBoost and IBG-Rare hosted Deniz Yilmaz Atakay, Head of the Rare Diseases Federation, for a productive
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