| The genetic landscape of the epileptic encephalopathies of infancy and childhood A McTague, KB Howell, JH Cross, MA Kurian, IE Scheffer The Lancet Neurology 15 (3), 304-316, 2016 | 629 | 2016 |
| Drug management for acute tonic‐clonic convulsions including convulsive status epilepticus in children A McTague, T Martland, R Appleton Cochrane Database of Systematic Reviews, 2018 | 385 | 2018 |
| Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis N Trump, A McTague, H Brittain, A Papandreou, E Meyer, A Ngoh, ... Journal of medical genetics 53 (5), 310-317, 2016 | 233 | 2016 |
| Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures T Stödberg, A McTague, AJ Ruiz, H Hirata, J Zhen, P Long, I Farabella, ... Nature communications 6 (1), 8038, 2015 | 162 | 2015 |
| Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum A McTague, R Appleton, S Avula, JH Cross, MD King, TS Jacques, ... Brain 136 (5), 1578-1591, 2013 | 150 | 2013 |
| Epilepsy and developmental disorders: Next generation sequencing in the clinic JD Symonds, A McTague European Journal of Paediatric Neurology 24, 15-23, 2020 | 132 | 2020 |
| Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial FJK O'Callaghan, SW Edwards, FD Alber, MC Borja, E Hancock, ... The Lancet Child & Adolescent Health 2 (10), 715-725, 2018 | 130 | 2018 |
| The genetic landscape of epilepsy of infancy with migrating focal seizures R Burgess, S Wang, A McTague, KE Boysen, X Yang, Q Zeng, KA Myers, ... Annals of neurology 86 (6), 821-831, 2019 | 118 | 2019 |
| Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy A McTague, U Nair, S Malhotra, E Meyer, N Trump, EV Gazina, ... Neurology 90 (1), e55-e66, 2018 | 117 | 2018 |
| GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome FR Danti, S Galosi, M Romani, M Montomoli, KJ Carss, FL Raymond, ... Neurology: Genetics 3 (2), e143, 2017 | 107 | 2017 |
| SLC25A22 is a novel gene for migrating partial seizures in infancy A Poduri, EL Heinzen, V Chitsazzadeh, FM Lasorsa, PC Elhosary, ... Annals of neurology 74 (6), 873-882, 2013 | 103 | 2013 |
| Treatment of epileptic encephalopathies A McTague, JH Cross CNS drugs 27, 175-184, 2013 | 98 | 2013 |
| Intravenous levetiracetam in acute repetitive seizures and status epilepticus in children: experience from a children's hospital A McTague, R Kneen, R Kumar, S Spinty, R Appleton Seizure 21 (7), 529-534, 2012 | 80 | 2012 |
| GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy A Papandreou, A McTague, N Trump, G Ambegaonkar, A Ngoh, E Meyer, ... Developmental Medicine & Child Neurology 58 (4), 416-420, 2016 | 77 | 2016 |
| The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications A Brunklaus, T Brünger, T Feng, C Fons, A Lehikoinen, E Panagiotakaki, ... Brain 145 (11), 3816-3831, 2022 | 65 | 2022 |
| Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia KM Gorman, E Meyer, D Grozeva, E Spinelli, A McTague, A Sanchis-Juan, ... The American Journal of Human Genetics 104 (5), 948-956, 2019 | 60 | 2019 |
| Delineation of the movement disorders associated with FOXG1 mutations A Papandreou, RB Schneider, EF Augustine, J Ng, K Mankad, E Meyer, ... Neurology 86 (19), 1794-1800, 2016 | 59 | 2016 |
| The expanding spectrum of movement disorders in genetic epilepsies A Papandreou, FR Danti, R Spaull, V Leuzzi, A Mctague, MA Kurian Developmental Medicine & Child Neurology 62 (2), 178-191, 2020 | 45 | 2020 |
| Genome editing in iPSC-based neural systems: from disease models to future therapeutic strategies A McTague, G Rossignoli, A Ferrini, S Barral, MA Kurian Frontiers in Genome Editing 3, 630600, 2021 | 38 | 2021 |
| The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction L Lenaerts, S Reynhout, I Verbinnen, F Laumonnier, A Toutain, ... Genetics in Medicine 23 (2), 352-362, 2021 | 33 | 2021 |
