معرفی
Dr. Stefan Barakat is a Researcher in the Department of Clinical Genetics at Erasmus MC. His work focuses on molecular genetics, neurodevelopmental disorders, and genetic disease mechanisms. He has led studies on histone pathologies, neurodevelopmental syndromes, and therapeutic avenues for conditions like Hirschsprung disease. Dr. Barakat has been recognized with prestigious awards including the ZonMw Vidi Award (2021) and VKGN Research Prize (2020).
- Education details are not explicitly provided in the text.
- Research collaborations span international networks, including The Undiagnosed Diseases Network and institutions worldwide.
His research emphasizes precision medicine, with breakthroughs such as identifying new disease genes (e.g., KDM2B, PPP2R5C) and leveraging zebrafish models for therapeutic discovery. Media highlights include coverage in Algemeen Dagblad and PZC, showcasing his work on undiagnosed genetic disorders.
- Grants: EpilepsieNL Research Grant (2022), CURE Epilepsy Award (2021).
- Labs/Teams: Collaborates with groups in genetics, molecular biology, and clinical research at Erasmus MC and global partners.
Stefan Barakat در سایتهای دیگر
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