Two‐year seizure reduction in adults with medically intractable partial onset epilepsy treated with responsive neurostimulation: final results of the RNS System Pivotal trial CN Heck, D King‐Stephens, AD Massey, DR Nair, BC Jobst, GL Barkley, ... Epilepsia 55 (3), 432-441, 2014 | 666 | 2014 |
Long-term treatment with responsive brain stimulation in adults with refractory partial seizures GK Bergey, MJ Morrell, EM Mizrahi, A Goldman, D King-Stephens, D Nair, ... Neurology 84 (8), 810-817, 2015 | 616 | 2015 |
Silent hippocampal seizures and spikes identified by foramen ovale electrodes in Alzheimer's disease AD Lam, G Deck, A Goldman, EN Eskandar, J Noebels, AJ Cole Nature medicine 23 (6), 678-680, 2017 | 352 | 2017 |
Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy T Klassen, C Davis, A Goldman, D Burgess, T Chen, D Wheeler, ... Cell 145 (7), 1036-1048, 2011 | 352 | 2011 |
Nine-year prospective efficacy and safety of brain-responsive neurostimulation for focal epilepsy DR Nair, KD Laxer, PB Weber, AM Murro, YD Park, GL Barkley, BJ Smith, ... Neurology 95 (9), e1244-e1256, 2020 | 322 | 2020 |
Brain‐responsive neurostimulation in patients with medically intractable seizures arising from eloquent and other neocortical areas BC Jobst, R Kapur, GL Barkley, CW Bazil, MJ Berg, GK Bergey, JG Boggs, ... Epilepsia 58 (6), 1005-1014, 2017 | 222 | 2017 |
Lateralization of mesial temporal lobe epilepsy with chronic ambulatory electrocorticography D King‐Stephens, E Mirro, PB Weber, KD Laxer, PC Van Ness, ... Epilepsia 56 (6), 959-967, 2015 | 176 | 2015 |
To share or not to share: a randomized trial of consent for data sharing in genome research AL McGuire, JM Oliver, MJ Slashinski, JL Graves, T Wang, PA Kelly, ... Genetics in Medicine 13 (11), 948-955, 2011 | 143 | 2011 |
DNA data sharing: research participants' perspectives AL McGuire, JA Hamilton, R Lunstroth, LB McCullough, A Goldman Genetics in Medicine 10 (1), 46-53, 2008 | 134 | 2008 |
Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention AM Goldman, ER Behr, C Semsarian, RD Bagnall, S Sisodiya, PN Cooper Epilepsia 57, 17-25, 2016 | 114 | 2016 |
Genetic generalized epilepsies SA Mullen, SF Berkovic, ILAE Genetics Commission, SF Berkovic, ... Epilepsia 59 (6), 1148-1153, 2018 | 106 | 2018 |
Brainstem network disruption: a pathway to sudden unexplained death in epilepsy? SG Mueller, M Nei, LM Bateman, R Knowlton, KD Laxer, D Friedman, ... Human brain mapping 39 (12), 4820-4830, 2018 | 99 | 2018 |
SCN1A testing for epilepsy: Application in clinical practice S Hirose, IE Scheffer, C Marini, P De Jonghe, E Andermann, AM Goldman, ... Epilepsia 54 (5), 946-952, 2013 | 94 | 2013 |
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes W Bi, J Yan, X Shi, LA Yuva-Paylor, BA Antalffy, A Goldman, JW Yoo, ... Human molecular genetics 16 (15), 1802-1813, 2007 | 93 | 2007 |
Mechanisms of sudden unexplained death in epilepsy AM Goldman Current opinion in neurology 28 (2), 166, 2015 | 70 | 2015 |
Channelopathy as a SUDEP biomarker in Dravet syndrome patient-derived cardiac myocytes CR Frasier, H Zhang, J Offord, LT Dang, DS Auerbach, H Shi, C Chen, ... Stem Cell Reports 11 (3), 626-634, 2018 | 53 | 2018 |
Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy TT Chen, TL Klassen, AM Goldman, C Marini, R Guerrini, JL Noebels Neurology 80 (12), 1078-1085, 2013 | 51 | 2013 |
Topical Review: Epilepsy and Chromosomal Rearrangements in Smith-Magenis Syndrome [del (17)(p11. 2p11. 2)] AM Goldman, L Potocki, K Walz, JK Lynch, DG Glaze, JR Lupski, ... Journal of child neurology 21 (2), 93-98, 2006 | 43 | 2006 |
De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures NA Batzir, PK Bhagwat, TN Eble, P Liu, CM Eng, SH Elsea, LA Robak, ... Molecular Case Studies 5 (3), a003673, 2019 | 39 | 2019 |
Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome D Marafi, B Suter, R Schultz, D Glaze, VN Pavlik, AM Goldman Neurology 92 (2), e108-e114, 2019 | 37 | 2019 |