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2022
Campbell, Ciaran 
ORCID: 0000-0001-8267-5252, Leu, Costin, Feng, Yen-Chen Anne, Wolking, Stefan ORCID: 0000-0002-1460-6623, Moreau, Claudia ORCID: 0000-0002-1480-3045, Ellis, Colin, Ganesan, Shiva, Martins, Helena, Oliver, Karen, Boothman, Isabelle ORCID: 0000-0002-3056-9121, Benson, Katherine, Molloy, Anne, Brody, Lawrence, Michaud, Jacques L., Hamdan, Fadi F., Minassian, Berge A., Lerche, Holger, Scheffer, Ingrid E., Sisodiya, Sanjay, Girard, Simon, Cosette, Patrick, Delanty, Norman, Lal, Dennis and Cavalleri, Gianpiero L.
(2022).
The role of common genetic variation in presumed monogenic epilepsies.
EBioMedicine, 81.
AMSTERDAM:
ELSEVIER.
ISSN 2352-3964
2020
Wolking, Stefan ORCID: 0000-0002-1460-6623, Schulz, Herbert, Nies, Anne T., McCormack, Mark, Schaeffeler, Elke, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Klein, Karl M., Krenn, Martin, Moller, Rikke S., Nikanorova, Marina, Weckhuysen, Sarah ORCID: 0000-0003-2878-1147, Cavalleri, Gianpiero L., Delanty, Norman, Depondt, Chantal, Johnson, Michael R., Koeleman, Bobby P. C., Kunz, Wolfram S., Marson, Anthony G., Sander, Josemir W., Sills, Graeme J., Striano, Pasquale ORCID: 0000-0002-6065-1476, Zara, Federico, Zimprich, Fritz, Weber, Yvonne G., Krause, Roland, Sisodiya, Sanjay, Schwab, Matthias, Sander, Thomas and Lerche, Holger
(2020).
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
Pharmacogenomics, 21 (5).
S. 325 - 336.
LONDON:
FUTURE MEDICINE LTD.
ISSN 1744-8042