On 8 June 2024, we are biking again with our Dutch colleagures to raise money for STXBP1-RD and to increase awareness for rare genetic epilepsies and neurodevelopmental disorders overall!
https://t.co/3CV9sr4Vua
#TeamSTXBP1, #ESCO, #Weckhuysen_lab
On June 11th, @Weckhuysen_team and colleagues at the CMN-VIB/UAntwerp/University Hospital Antwerp bike 170 km together with our colleagues of the VU Amsterdam to collect funding for research into novel therapies for STXBP1-encephalopathy. More info through link.
Very happy to have contributed to this preprint on de novo FZR1 variants in patients with Developmental and Epileptic Encephalopathies with @SathiyaManivan1 and @JolienRoovers https://t.co/NGG0gybSmc
We are hiring! We are looking for a postdoc to join our team to work on Kv7-associated encephalopathies using iPSC-derived models. https://t.co/TXKq2C3y2y
Our research group is hiring! We're looking for a PhD candidate interested in studying autophagy in vitro as well as in vivo - all details below: https://t.co/xDRgkYarKD
Very happy to have still shared some music with my orchestra during lockdown :)
I See You - Antwerpse Studentenharmonie arr. Johnnie Vinson https://t.co/2SFF2LuEAS via @YouTube
Beijer and Baets review the current genetic landscape of hereditary motor neuropathies, highlighting recent reports of novel genes/mutations and discoveries related to disease mechanisms. https://t.co/38X6CSFVZs
Meet @TejasSNiranjan our new post-doctoral researcher. Tejas conducts deep analysis of whole exome & and whole genome sequencing to unravel the genetic causes of Epilepsy and the Developmental and Epileptic Encephalopathies. @CMN_VIB
Just found this amazing (and fun) podcast about living with epilepsy and the importance of talking about it! #EpilepsyAwarenessMonth
Ep. #016 | HEALTH | Living With Epilepsy | Kristina's Story https://t.co/rYYYn6ywSl via @ListenNotes
Interested in precision medicine in genetic epilepsy? Join us at the 4th international Dianalund conference on Epilepsy and learn where we are, and what is next! Tune in Thursday to hear @SWeckhuysen talk about KCNQ2-Encephalopathy.
Meet our PostDoc/MD @HannahStamberg1 who just published her work with @ingridscheffer and @FiladelfiaGene1 on NEXMIF-encefalopathy in @GIMJournal https://t.co/Uwh8IAiibK. Hannah focuses on epilepsy gene discovery & validation, and in depth genotype-phenotype correlation studies.
Meet @C_Millevert our new clinical PhD. As MD she will be working on the discovering of genetic modifiers associated with KCNQ2-encefalopathy, mosaic brain mutations in resected brain tissue of patients with refractory epilepsy and (precision) therapeutic studies.@CMN_VIB
Meet @DirkxNina, a @FWOVlaanderen phd student and #steminist. Nina's research is focussed on unraveling the underlying mechanisms of KCNQ2-Encephalopathy using iPSC-derived neuronal cultures. @Kcnq2Cure@CMN_VIB
November is #EpilepsyAwarenessMonth. A perfect time to introduce the @Weckhuysen_team, who focus on the identification of genes and genetic mechanisms underlying epilepsy.