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| | Publication Year | Title | Author(s) |
| 121 | 30-Oct-2014 | Conceptualizing lennox-gastaut syndrome as a secondary network epilepsy. | Archer, John S ; Warren, Aaron E L; Jackson, Graeme D ; Abbott, David F |
| 122 | 26-Dec-2001 | Concussion: the history of clinical and pathophysiological concepts and misconceptions. | McCrory, Paul; Berkovic, Samuel F |
| 123 | 5-Jan-2015 | Constructing Carbon Fiber Motion-Detection Loops for Simultaneous EEG-fMRI. | Abbott, David F ; Masterton, Richard A J; Archer, John S ; Fleming, Steven W; Warren, Aaron E L; Jackson, Graeme D |
| 124 | 2021 | Contribution of rare genetic variants to drug response in absence epilepsy. | Myers, Kenneth A; Bennett, Mark F ; Grinton, Bronwyn E; Dabscheck, Gabriel; Chan, Eunice K; Bello-Espinosa, Luis E; Sadleir, Lynette G; D'Alfonso, Sabrina; Schneider, Amy L ; Damiano, John A; Hildebrand, Michael S ; Bahlo, Melanie; Berkovic, Samuel F ; Buchhalter, Jeffrey; Scheffer, Ingrid E |
| 125 | 1-Jun-2023 | Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy. | Khoshkhoo, Sattar; Wang, Yilan; Chahine, Yasmine; Erson-Omay, E Zeynep; Robert, Stephanie M; Kiziltug, Emre; Damisah, Eyiyemisi C; Nelson-Williams, Carol; Zhu, Guangya; Kong, Wenna; Huang, August Yue; Stronge, Edward; Phillips, H Westley; Chhouk, Brian H; Bizzotto, Sara; Chen, Ming Hui; Adikari, Thiuni N; Ye, Zimeng; Witkowski, Tom ; Lai, Dulcie; Lee, Nadine; Lokan, Julie ; Scheffer, Ingrid E ; Berkovic, Samuel F ; Haider, Shozeb; Hildebrand, Michael S ; Yang, Edward; Gunel, Murat; Lifton, Richard P; Richardson, R Mark; Blümcke, Ingmar; Alexandrescu, Sanda; Huttner, Anita; Heinzen, Erin L; Zhu, Jidong; Poduri, Annapurna; DeLanerolle, Nihal; Spencer, Dennis D; Lee, Eunjung Alice; Walsh, Christopher A; Kahle, Kristopher T |
| 6 | 25-Sep-2013 | Copy number variants are frequent in genetic generalized epilepsy with intellectual disability. | Mullen, Saul A ; Carvill, Gemma L; Bellows, Susannah; Bayly, Marta A; Trucks, Holger; Lal, Dennis; Sander, Thoman; Berkovic, Samuel F ; Dibbens, Leanne M; Scheffer, Ingrid E ; Mefford, Heather C |
| 7 | 1-Jan-2010 | Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies. | Scheffer, Ingrid E ; Berkovic, Samuel F |
| 8 | 11-Aug-2010 | The core network in absence epilepsy. Differences in cortical and thalamic BOLD response. | Carney, Patrick W ; Masterton, Richard A J; Harvey, A Simon; Scheffer, Ingrid E ; Berkovic, Samuel F ; Jackson, Graeme D |
| 9 | 4-Dec-2019 | Correction to: Serum sodium and intracranial pressure changes after desmopressin therapy in severe traumatic brain injury patients: a multi-centre cohort study. | Harrois, A; Anstey, J R; Taccone, F S; Udy, A A; Citerio, G; Duranteau, J; Ichai, C; Badenes, R; Prowle, J R; Ercole, A; Oddo, M; Schneider, A ; van der Jagt, M; Wolf, S; Helbok, R; Nelson, D W; Skrifvars, M B; Cooper, D J; Bellomo, Rinaldo |
| 10 | 10-Aug-2018 | Corrigendum to "Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome" [Epilepsy Res. 140 (2018) 166-170]. | Myers, Kenneth A; White, Susan M; Mohammed, Shehla; Metcalfe, Kay A; Fry, Andrew E; Wraige, Elisabeth; Vasudevan, Pradeep C; Balasubramanian, Meena; Scheffer, Ingrid E |
| 11 | Oct-2020 | Cortex leads the thalamic centromedian nucleus in generalized epileptic discharges in Lennox-Gastaut syndrome. | Dalic, Linda J ; Warren, Aaron E L; Young, James C; Thevathasan, Wesley; Roten, Annie ; Bulluss, Kristian J ; Archer, John S |
| 12 | 3-Dec-2012 | Cortical excitability and refractory epilepsy: a three-year longitudinal transcranial magnetic stimulation study. | Badawy, Radwa A B; Jackson, Graeme D ; Berkovic, Samuel F ; Macdonell, Richard A L |
| 13 | 1-Jan-1993 | Cortical hyperexcitability in progressive myoclonus epilepsy: a study with transcranial magnetic stimulation. | Reutens, David C; Puce, Aina; Berkovic, Samuel F |
| 14 | 4-Mar-2015 | Cortical microarchitecture changes in genetic epilepsy. | Wimmer, Verena C; Li, Melody Y-S; Berkovic, Samuel F ; Petrou, Steven |
| 15 | 2022 | COVID-19 vaccine in patients with Dravet syndrome: Observations and real-world experiences. | Hood, Veronica; Berg, Anne T; Knupp, Kelly G; Koh, Sookyong; Laux, Linda; Meskis, Mary Anne; Zulfiqar-Ali, Quratulain; Perry, M Scott; Scheffer, Ingrid E ; Sullivan, Joseph; Wirrell, Elaine; Andrade, Danielle M |
| 16 | 2021 | Cutting Edge Approaches to Detecting Brain Mosaicism Associated with Common Focal Epilepsies: Implications for Diagnosis and Potential therapies. | Ye, Zimeng; Bennett, Mark F ; Bahlo, Melanie; Scheffer, Ingrid E ; Berkovic, Samuel F ; Perucca, Piero ; Hildebrand, Michael S |
| 17 | Jul-2020 | Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy. | Carvill, Gemma L; Helbig, Katherine L; Myers, Candace T; Scala, Marcello; Huether, Robert; Lewis, Sara; Kruer, Tyler N; Guida, Brandon S; Bakhtiari, Somayeh; Sebe, Joy; Tang, Sha; Stickney, Heather; Oktay, Sehribani Ulusoy; Bhandiwad, Ashwin A; Ramsey, Keri; Narayanan, Vinodh; Feyma, Timothy; Rohena, Luis O; Accogli, Andrea; Severino, Mariasavina; Hollingsworth, Georgina; Gill, Deepak; Depienne, Christel; Nava, Caroline; Sadleir, Lynette G; Caruso, Paul A; Lin, Angela E; Jansen, Floor E; Koeleman, Bobby; Brilstra, Eva; Willemsen, Marjolein H; Kleefstra, Tjitske; Sa, Joaquim; Mathieu, Marie-Laure; Perrin, Laurine; Lesca, Gaetan; Striano, Pasquale; Casari, Giorgio; Scheffer, Ingrid E ; Raible, David; Sattlegger, Evelyn; Capra, Valeria; Padilla-Lopez, Sergio; Mefford, Heather C; Kruer, Michael C |
| 18 | Feb-2022 | DBS of thalamic centromedian nucleus for Lennox-Gastaut syndrome (ESTEL trial). | Dalic, Linda J ; Warren, Aaron E L; Bulluss, Kristian J ; Thevathasan, Wesley; Roten, Annie ; Churilov, Leonid ; Archer, John S |
| 19 | 2-Aug-2018 | De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. | Gregor, Anne; Sadleir, Lynette G; Asadollahi, Reza; Azzarello-Burri, Silvia; Battaglia, Agatino; Ousager, Lilian Bomme; Boonsawat, Paranchai; Bruel, Ange-Line; Buchert, Rebecca; Calpena, Eduardo; Cogné, Benjamin; Dallapiccola, Bruno; Distelmaier, Felix; Elmslie, Frances; Faivre, Laurence; Haack, Tobias B; Harrison, Victoria; Henderson, Alex; Hunt, David; Isidor, Bertrand; Joset, Pascal; Kumada, Satoko; Lachmeijer, Augusta M A; Lees, Melissa; Lynch, Sally Ann; Martinez, Francisco; Matsumoto, Naomichi; McDougall, Carey; Mefford, Heather C; Miyake, Noriko; Myers, Candace T; Moutton, Sébastien; Nesbitt, Addie; Novelli, Antonio; Orellana, Carmen; Rauch, Anita; Rosello, Monica; Saida, Ken; Santani, Avni B; Sarkar, Ajoy; Scheffer, Ingrid E ; Shinawi, Marwan; Steindl, Katharina; Symonds, Joseph D; Zackai, Elaine H; Reis, André; Sticht, Heinrich; Zweier, Christiane |
| 20 | 1-Jun-2006 | De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study. | Berkovic, Samuel F ; Harkin, Louise A; McMahon, Jacinta M; Pelekanos, James T; Zuberi, Sameer M; Wirrell, Elaine C; Gill, Deepak S; Iona, Xenia; Mulley, John C; Scheffer, Ingrid E |
