Dr Sid is our SETBP1 Clinician we are highlighting in our new series called Meet the SETBP1 Team! In this series, we share interviews and stories from our SETBP1 families, SETBP1 clinicians, SETBP1 Board members, and SETBP1 researchers. Dr Sid joined our SETBP1 community the same year SETBP1 Society formed. He is a pediatric neurologist […]
Next up in our Meet the SETBP1 Team series is Dr Carl Ernst! Carl Ernst, PhD is a researcher at the Douglas Research Centre, professor at McGill University and Canada research chair in psychiatric genetics in Montreal, Canada. His lab’s expertise is in stem cell modelling of neurological disease and genetic engineering. He has a […]
Next up in our Meet the SETBP1 Team series is Prof Dr Simon Fisher! He is a geneticist, neuroscientist and director of the Max Planck Institute for Psycholinguistics in Nijmegen, the Netherlands. Simon’s work attempts to bridge the gaps between genes, brains, speech and language, by integrating molecular findings with data from levels of analysis, […]
SETBP1 Society is a member of COMBINEDBrain a non-profit consortium of 25 patient-advocacy groups, each representing a different rare genetic neurodevelopmental disorder. COMBINEDBrain’s mission is to speed clinical trial readiness for severe rare neurodevelopmental disorders by pooling resources and working together across all of our member disorders. We are honored to participate in COMBINEDBrain and […]
We are excited to kick off a new series called Meet the SETBP1 Team! In this series, we will share interviews and stories from our SETBP1 families, SETBP1 clinicians, SETBP1 Board members, and SETBP1 researchers. Our clinical geneticist who has been on this journey with us since before SETBP1 Society formed, Dr Bregje van Bon, […]
