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Testing association of rare genetic variants with resistance to three common antiseizure medications
Authors:Stefan Wolking  Claudia Moreau  Anne T. Nies  Elke Schaeffeler  Mark McCormack  Pauls Auce  Andreja Avbersek  Felicitas Becker  Martin Krenn  Rikke S. Møller  Marina Nikanorova  Yvonne G. Weber  Sarah Weckhuysen  Gianpiero L. Cavalleri  Norman Delanty  Chantal Depondt  Michael R. Johnson  Bobby P.C. Koeleman  Wolfram S. Kunz  Anthony G. Marson  Josemir W. Sander  Graeme J. Sills  Pasquale Striano  Federico Zara  Fritz Zimprich  Matthias Schwab  Roland Krause  Sanjay M. Sisodiya  Patrick Cossette  Simon L. Girard  Holger Lerche  EpiPGX Consortium
Affiliation:1. Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany;2. Department of Applied Sciences, University of Quebec in Chicoutimi, Saguenay, Canada;3. Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany;4. Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany

University of Tübingen, Tübingen, Germany;5. Molecular and Cellular Therapeutics, Royal College of Surgeons in Ireland, Dublin, Ireland;6. Walton Centre NHS Foundation Trust, Liverpool, UK;7. Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK

Chalfont Centre for Epilepsy, London, UK;8. Department of Neurology, Medical University of Vienna, Vienna, Austria;9. Danish Epilepsy Centre - Filadelfia, Dianalund, Denmark;10. Department of Regional Health Research, University of Southern Denmark, Odense, Denmark;11. Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany

Department of Epileptology and Neurology, University of Aachen, Aachen, Germany;12. Neurogenetics Group, VIB-UAntwerp, Center for Molecular Neurology, Antwerp, Belgium

Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium

Department of Neurology, Antwerp University Hospital, Antwerp, Belgium;13. Department of Neurology, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium;14. Division of Brain Sciences, Imperial College Faculty of Medicine, London, UK;15. Department of Genetics, University Medical Center Utrecht, Utrecht, Netherlands;16. Institute of Experimental Epileptology and Cognition Research and Department of Epileptology, University of Bonn, Bonn, Germany;17. Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK;18. Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK

Chalfont Centre for Epilepsy, London, UK

Stichting Epilepsie Instellingen Nederland (SEIN), Heemstede, Netherlands;19. IRCCS "G. Gaslini" Institute, Genova, Italy;20. Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy;21. Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany

University of Tübingen, Tübingen, Germany

Department of Clinical Pharmacology, Pharmacy and Biochemistry, University Tübingen, Tübingen, Germany;22. Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg;23. Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK;24. Department of Neurosciences, Research Center of the University of Montreal Hospital Center (CRCHUM), University of Montreal, Montreal, Canada

Abstract:
Keywords:burden analysis  lamotrigine  levetiracetam  pharmacogenomics  rare variants  valproic acid
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