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-causing mutations. Finally, we will validate the identified key (epi)genetic molecular and eplore their therapeutic potential in in vitro and in vivo disease models. Profile The candidate should: have an
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short and long-read sequencing and transcriptomics, and iPSC-based disease modeling to better understand the genetic etiologies of intractable epilepsy. The team is part of the European STXBP1 consortium
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, will serve as input to generate a statistical prediction model, that will be built together with the bioinformatics team. You will publish scientific articles related to the research project, disseminate
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biological and CRISPR/CAS9 technologies and organoid models derived from CRC patients. You will publish scientific articles related to the research project and will participate to scientific conferences
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from human genetics, genomics, protein biochemistry and neuronal and glial cell biology to integrative systems and computational biology. Models include yeast, fly, mouse, and pluripotent human cell
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frequently asked questions or send an email to jobs@uantwerpen.be . Questions about the scientific content of the position can be asked to Prof. Joke Hadermann, joke.hadermann@uantwerpen.be . The University
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about the online application form, please check the frequently asked questions or send an email to jobs@uantwerpen.be . Questions about the scientific content of the position can be asked to Prof. Joke
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, please check the frequently asked questions or send an email to jobs@uantwerpen.be . If you have any questions about the job itself, please contact Dr. Julia Heinemann (Julia.heinemann@uantwerpen.be
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about the online application form, please check the frequently asked questions or send an email to jobs@uantwerpen.be . If you have any questions about the job itself or for additional information
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. If you have any questions about the online application form, please check the frequently asked questions or send an email to jobs@uantwerpen.be . If you have any questions about the job itself, please