Milí kolegové a kolegyně,
chtěli bychom vás srdečně pozvat na další přednášku semináře, která se koná ve středu 11.4.2018 od 17:20 v posluchárně S4.
Hostem na semináři bude Dr Viorica Chelban z University College London a téma přednášky bude
Disease discovery in neurogenetics: from patient to pathways and therapies
Těšíme se srdečně na vaši účast!
Za všechny organizátory semináře s pozdravem, Petr Daněček
Stránky semináře http://bioinformatika.mff.cuni.cz/seminar/
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Dr. Viorica Chelban is a neurologist and a Member of the Royal College of Physicians UK doing her research at the National Hospital for Neurology and Neurosurgery and the Institute of Neurology, University College London. Having recently described several new genetic disorders Dr Chelban was awarded a Clinical Research Fellowship by the Association of British Neurologists for her work in neurogenetics and rare diseases.
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Viorica Chelban
Institute of Neurology, University College London
In this talk I will speak about neurogenetics and its methods. Neurogenetics combines bioinformatics with functional and clinical work as a means of discovery of new mechanisms in human neurological conditions. Genetic methods are increasingly used in diagnosis and treatment. The aim of the talk is to raise interest and awareness of the complex relationships in human genetics, pitfalls and challenges of handling the millions of data points involved in genetic studies of diseases and the complexity of validation of such results in patients.
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