Research on Rahman Syndrome delivers a novel tool to study the rare genetic condition
IBG Rare and Undiagnosed Diseases Platform Member Dr. Kasim Diril’s group published a study on Rahman Syndrome in FEBS Open Bio
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Meeting Announcement – Variants of Uncertain Clinical Significance (VUS) in Pediatric Neurology Practice and Suggestions for Solutions
On January 13, 2024, between 12.45-16.15, a half-day hybrid meeting titled “Variants of Uncertain Clinical Significance (VUS) in Pediatric Neurology
Read MoreRareboost External Seminar Announcement – Prof. Dr. Ahmet Özen
We are pleased to announce an upcoming seminar featuring Prof. Dr. Ahmet Özen, a leading expert in the field of
Read MoreRare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop
As part of the RareBoost project, “Rare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop” was held
Read MoreApplication period ended – Scientific Communication Officer
Offer Description The Izmir Biomedicine and Genome Center (IBG) is seeking a skilled Scientific Communications Officer for the RareBoost project (#
Read MoreApplication period ended – Postdoctoral researchers, Ph.D. student, Research technicians and laboratory managers
Among the applicants: Postdoctoral researchers (qualified candidates with a strong background in various fields of biomedical sciences and a strong
Read MoreApplication period ended – Training Officer
Position: Training Officer (in a researcher environment) Description: The Izmir Biomedicine and Genome Center (IBG, Turkey; www.ibg.edu.tr) is searching for a Training
Read MoreRare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop
Within the scope of the RareBoost ERA Chair project supported by the European Union H2020 program at Izmir Biomedicine and
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