| De novo mutations in epileptic encephalopathies AS Allen, SF Berkovic, P Cossette, N Delanty, D Dlugos, EE Eichler, ... Nature 501 (7466), 217, 2013 | 632 | 2013 |
| Somatic mutation, genomic variation, and neurological disease A Poduri, GD Evrony, X Cai, CA Walsh Science 341 (6141), 1237758, 2013 | 379 | 2013 |
| Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain GD Evrony, X Cai, E Lee, LB Hills, PC Elhosary, HS Lehmann, JJ Parker, ... Cell 151 (3), 483-496, 2012 | 376 | 2012 |
| De novo mutations in epileptic encephalopathies KC Epi, PE Phenome, AS Allen, SF Berkovic, P Cossette, N Delanty, ... Nature 501 (7466), 217-221, 2013 | 368 | 2013 |
| Using whole-exome sequencing to identify inherited causes of autism WY Timothy, MH Chahrour, ME Coulter, S Jiralerspong, K Okamura-Ikeda, ... Neuron 77 (2), 259-273, 2013 | 354 | 2013 |
| Somatic activation of AKT3 causes hemispheric developmental brain malformations A Poduri, GD Evrony, X Cai, PC Elhosary, R Beroukhim, MK Lehtinen, ... Neuron 74 (1), 41-48, 2012 | 316 | 2012 |
| Microdeletion/duplication at 15q13. 2q13. 3 among individuals with features of autism and other neuropsychiatric disorders DT Miller, Y Shen, LA Weiss, J Korn, I Anselm, C Bridgemohan, GF Cox, ... Journal of medical genetics 46 (4), 242-248, 2009 | 310 | 2009 |
| Somatic mutations in cerebral cortical malformations SS Jamuar, ATN Lam, M Kircher, AM D’Gama, J Wang, BJ Barry, X Zhang, ... New England Journal of Medicine 371 (8), 733-743, 2014 | 201 | 2014 |
| De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ... The American Journal of Human Genetics 95 (4), 360-370, 2014 | 190 | 2014 |
| Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain X Cai, GD Evrony, HS Lehmann, PC Elhosary, BK Mehta, A Poduri, ... Cell reports 8 (5), 1280-1289, 2014 | 184 | 2014 |
| Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia AM D'Gama, Y Geng, JA Couto, B Martin, EA Boyle, CM LaCoursiere, ... Annals of neurology 77 (4), 720-725, 2015 | 151 | 2015 |
| Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients S Weckhuysen, V Ivanovic, R Hendrickx, R Van Coster, H Hjalgrim, ... Neurology 81 (19), 1697-1703, 2013 | 128 | 2013 |
| Epilepsy genetics—past, present, and future A Poduri, D Lowenstein Current opinion in genetics & development 21 (3), 325-332, 2011 | 124 | 2011 |
| Copy number variation plays an important role in clinical epilepsy H Olson, Y Shen, J Avallone, BR Sheidley, R Pinsky, AM Bergin, GT Berry, ... Annals of neurology 75 (6), 943-958, 2014 | 112 | 2014 |
| SCN2A encephalopathy: a major cause of epilepsy of infancy with migrating focal seizures KB Howell, JM McMahon, GL Carvill, D Tambunan, MT Mackay, ... Neurology 85 (11), 958-966, 2015 | 105 | 2015 |
| Trends in resource utilization by children with neurological impairment in the United States inpatient health care system: a repeat cross-sectional study JG Berry, A Poduri, JL Bonkowsky, J Zhou, DA Graham, C Welch, ... PLoS medicine 9 (1), e1001158, 2012 | 98 | 2012 |
| De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies CT Myers, JM McMahon, AL Schneider, S Petrovski, AS Allen, GL Carvill, ... The American Journal of Human Genetics 99 (2), 287-298, 2016 | 90 | 2016 |
| Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures X Zhang, J Ling, G Barcia, L Jing, J Wu, BJ Barry, GH Mochida, RS Hill, ... The American Journal of Human Genetics 94 (4), 547-558, 2014 | 89 | 2014 |
| Altered inhibition in tuberous sclerosis and type IIb cortical dysplasia DM Talos, H Sun, B Kosaras, A Joseph, RD Folkerth, A Poduri, ... Annals of neurology 71 (4), 539-551, 2012 | 86 | 2012 |
| Apolipoprotein E4 and beta amyloid in senile plaques and cerebral blood vessels of aged rhesus monkeys. A Poduri, M Gearing, GW Rebeck, SS Mirra, J Tigges, BT Hyman The American journal of pathology 144 (6), 1183, 1994 | 86 | 1994 |
