| Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature S Wolking, E Schaeffeler, H Lerche, M Schwab, AT Nies Clinical pharmacokinetics 54, 709-735, 2015 | 295 | 2015 |
| Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019 | 262 | 2019 |
| Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study P May, S Girard, M Harrer, DR Bobbili, J Schubert, S Wolking, F Becker, ... The Lancet Neurology 17 (8), 699-708, 2018 | 95 | 2018 |
| Carbamazepine‐and oxcarbazepine‐induced hyponatremia in people with epilepsy B Berghuis, J van der Palen, GJ de Haan, D Lindhout, BPC Koeleman, ... Epilepsia 58 (7), 1227-1233, 2017 | 87 | 2017 |
| Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies MF Dohrn, N Glöckle, L Mulahasanovic, C Heller, J Mohr, C Bauer, ... Journal of neurochemistry 143 (5), 507-522, 2017 | 80 | 2017 |
| Antagonism of the mammalian target of rapamycin selectively mediates metabolic effects of epidermal growth factor receptor inhibition and protects human malignant glioma cells … MW Ronellenfitsch, DP Brucker, MC Burger, S Wolking, F Tritschler, ... Brain 132 (6), 1509-1522, 2009 | 64 | 2009 |
| Clinical spectrum of STX1B-related epileptic disorders S Wolking, P May, D Mei, RS Møller, S Balestrini, KL Helbig, CD Altuzarra, ... Neurology 92 (11), e1238-e1249, 2019 | 63 | 2019 |
| Early-onset familial hemiplegic migraine due to a novel SCN1A mutation C Fan, S Wolking, F Lehmann-Horn, UBS Hedrich, T Freilinger, H Lerche, ... Cephalalgia 36 (13), 1238-1247, 2016 | 60 | 2016 |
| The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathies A Grimm, M Rasenack, IM Athanasopoulou, NM Dammeier, C Lipski, ... Journal of neurology 263, 221-230, 2016 | 54 | 2016 |
| Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients M McCormack, H Gui, A Ingason, D Speed, GEB Wright, EJ Zhang, ... Neurology 90 (4), e332-e341, 2018 | 49 | 2018 |
| Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals JE Motelow, G Povysil, RS Dhindsa, KE Stanley, AS Allen, YCA Feng, ... The American Journal of Human Genetics 108 (6), 965-982, 2021 | 45 | 2021 |
| Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy K Silvennoinen, N de Lange, S Zagaglia, S Balestrini, G Androsova, ... Epilepsia Open 4 (3), 420-430, 2019 | 44 | 2019 |
| Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis G Androsova, R Krause, M Borghei, M Wassenaar, P Auce, A Avbersek, ... Epilepsia 58 (10), 1734-1741, 2017 | 44 | 2017 |
| Focal epilepsy in glucose transporter type 1 (Glut1) defects: case reports and a review of literature S Wolking, F Becker, T Bast, A Wiemer-Kruel, T Mayer, H Lerche, ... Journal of neurology 261, 1881-1886, 2014 | 36 | 2014 |
| Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study S Wolking, H Schulz, AT Nies, M McCormack, E Schaeffeler, P Auce, ... Pharmacogenomics 21 (5), 325-335, 2020 | 31 | 2020 |
| Testing association of rare genetic variants with resistance to three common antiseizure medications S Wolking, C Moreau, AT Nies, E Schaeffeler, M McCormack, P Auce, ... Epilepsia 61 (4), 657-666, 2020 | 29 | 2020 |
| Polygenic risk scores of several subtypes of epilepsies in a founder population C Moreau, RM Rébillard, S Wolking, J Michaud, F Tremblay, A Girard, ... Neurology: Genetics 6 (3), e416, 2020 | 27 | 2020 |
| The role of common genetic variation in presumed monogenic epilepsies C Campbell, C Leu, YCA Feng, S Wolking, C Moreau, C Ellis, S Ganesan, ... EBioMedicine 81, 2022 | 24 | 2022 |
| Genetic testing before epilepsy surgery–An exploratory survey and case collection from German epilepsy centers CM Boßelmann, V San Antonio-Arce, A Schulze-Bonhage, S Fauser, ... Seizure 95, 4-10, 2022 | 24 | 2022 |
| Assessing the role of rare genetic variants in drug‐resistant, non‐lesional focal epilepsy S Wolking, C Moreau, M McCormack, R Krause, M Krenn, ... Annals of clinical and translational neurology 8 (7), 1376-1387, 2021 | 23 | 2021 |
