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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