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| | Publication Year | Title | Author(s) |
| 361 | 22-Jan-2023 | GABAA receptor neurotransmission & epilepsy: principles, disease mechanisms & pharmacotherapy. | Bryson, Alexander ; Reid, Christopher; Petrou, Steven |
| 362 | 12-Mar-2014 | GABRA1 and STXBP1: novel genetic causes of Dravet syndrome. | Carvill, Gemma L; Weckhuysen, Sarah; McMahon, Jacinta M; Hartmann, Corinna; Møller, Rikke S; Hjalgrim, Helle; Cook, Joseph; Geraghty, Eileen; O'Roak, Brian J; Petrou, Steven; Clarke, Alison; Gill, Deepak S; Sadleir, Lynette G; Muhle, Hiltrud; von Spiczak, Sarah; Nikanorova, Marina; Hodgson, Bree L; Gazina, Elena V; Suls, Arvid; Shendure, Jay; Dibbens, Leanne M; De Jonghe, Peter; Helbig, Ingo; Berkovic, Samuel F ; Scheffer, Ingrid E ; Mefford, Heather C |
| 363 | Feb-2018 | Gain-of-function HCN2 variants in genetic epilepsy. | Li, Melody; Maljevic, Snezana; Phillips, A Marie; Petrovski, Slave; Hildebrand, Michael S ; Burgess, Rosemary; Mount, Therese; Zara, Federico; Striano, Pasquale; Schubert, Julian; Thiele, Holger; Nürnberg, Peter; Wong, Michael; Weisenberg, Judith L; Thio, Liu Lin; Lerche, Holger; Scheffer, Ingrid E ; Berkovic, Samuel F ; Petrou, Steven; Reid, Christopher A |
| 24 | 24-Apr-2008 | Gene expression analysis in absence epilepsy using a monozygotic twin design. | Helbig, Ingo; Matigian, Nicholas A; Vadlamudi, Lata; Lawrence, Kate M; Bayly, Marta A; Bain, Sharon M; Diyagama, Dileepa; Scheffer, Ingrid E ; Mulley, John C; Holloway, Andrew J; Dibbens, Leanne M; Berkovic, Samuel F ; Hayward, Nicholas K |
| 25 | 1-Jan-1999 | Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome. | Singh, R; Scheffer, Ingrid E ; Crossland, K; Berkovic, Samuel F |
| 26 | Dec-2020 | Generalized, focal, and combined epilepsies in families: New evidence for distinct genetic factors. | Ellis, Colin A; Ottman, Ruth; Epstein, Michael P; Berkovic, Samuel F |
| 27 | Aug-2019 | Genetic absence epilepsy: Effective connectivity from piriform cortex to mediodorsal thalamus. | Young, James C; Paolini, Antonio G; Pedersen, Mangor; Jackson, Graeme D |
| 28 | 1-Aug-2014 | Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases. | Bagnall, Richard D; Crompton, Douglas E; Cutmore, Carina; Regan, Brigid M; Berkovic, Samuel F ; Scheffer, Ingrid E ; Semsarian, Christopher |
| 29 | 1-May-2004 | Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families. | Marini, Carla; Scheffer, Ingrid E ; Crossland, Kathryn M; Grinton, Bronwyn E; Phillips, Fiona L; McMahon, Jacinta M; Turner, Samantha J; Dean, Joanne T; Kivity, Sara; Mazarib, Aziz; Neufeld, Miriam Y; Korczyn, Amos D; Harkin, Louise A; Dibbens, Leanne M; Wallace, Robyn H; Mulley, John C; Berkovic, Samuel F |
| 30 | 2016 | Genetic Associations With White Matter Hyperintensities Confer Risk of Lacunar Stroke. | Traylor, Matthew; Rutten-Jacobs, Loes C A; Thijs, Vincent N ; Holliday, Elizabeth G; Levi, Chris; Bevan, Steve; Malik, Rainer; Boncoraglio, Giorgio; Sudlow, Cathie; Rothwell, Peter M; Dichgans, Martin; Markus, Hugh S |
| 31 | 26-Aug-2020 | Genetic characterisation identifies bottom-of-sulcus dysplasia as an mTORopathy. | Lee, Wei Shern; Stephenson, Sarah Em; Pope, Kate; Gillies, Greta; Maixner, Wirginia; Macdonald-Laurs, Emma; MacGregor, Duncan; D'Arcy, Colleen; Jackson, Graeme D ; Harvey, A Simon; Leventer, Richard J; Lockhart, Paul J |
| 32 | 29-Sep-2020 | Genetic Contributions to Acquired Epilepsies. | Perucca, Piero ; Scheffer, Ingrid E |
| 33 | 19-Sep-2017 | Genetic epilepsy with febrile seizures plus: refining the spectrum | Zhang, Yue-Hua; Burgess, Rosemary; Malone, Jodie P; Glubb, Georgie C; Helbig, Katherine L; Vadlamudi, Lata; Kivity, Sara; Afawi, Zaid; Bleasel, Andrew; Grattan-Smith, Padraic; Grinton, Bronwyn E; Bellows, Susannah T; Vears, Danya F; Damiano, John A; Goldberg-Stern, Hadassa; Korczyn, Amos D; Dibbens, Leanne M; Ruzzo, Elizabeth K; Hildebrand, Michael S ; Berkovic, Samuel F ; Scheffer, Ingrid E |
| 34 | 6-May-2022 | Genetic factors and shared environment contribute equally to objective singing ability. | Yeom, Daniel; Tan, Yi Ting; Haslam, Nick; Mosing, Miriam A; Yap, Valerie M Z; Fraser, Trisnasari; Hildebrand, Michael S ; Berkovic, Samuel F ; McPherson, Gary E; Peretz, Isabelle; Wilson, Sarah J |
| 35 | Jun-2018 | Genetic generalized epilepsies. | Mullen, Saul A ; Berkovic, Samuel F |
| 36 | Feb-2019 | Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke. | Pfeiffer, Dorothea; Chen, Bowang; Schlicht, Kristina; Ginsbach, Philip; Abboud, Sherine; Bersano, Anna; Bevan, Steve; Brandt, Tobias; Caso, Valeria; Debette, Stéphanie; Erhart, Philipp; Freitag-Wolf, Sandra; Giacalone, Giacomo; Grau, Armin J; Hayani, Eyad; Jern, Christina; Jiménez-Conde, Jordi; Kloss, Manja; Krawczak, Michael; Lee, Jin-Moo; Lemmens, Robin; Leys, Didier; Lichy, Christoph; Maguire, Jane M; Martin, Juan J; Metso, Antti J; Metso, Tiina M; Mitchell, Braxton D; Pezzini, Alessandro; Rosand, Jonathan; Rost, Natalia S; Stenman, Martin; Tatlisumak, Turgut; Thijs, Vincent N ; Touzé, Emmanuel; Traenka, Christopher; Werner, Inge; Woo, Daniel; Del Zotto, Elisabetta; Engelter, Stefan T; Kittner, Steven J; Cole, John W; Grond-Ginsbach, Caspar; Lyrer, Philippe A; Lindgren, Arne |
| 37 | 3-Oct-2023 | Genetic Insights on the Relation of Vascular Risk Factors and Cervical Artery Dissection. | Le Grand, Quentin; Ecker Ferreira, Leslie; Metso, Tiina M; Schilling, Sabrina; Tatlisumak, Turgut; Grond-Ginsbach, Caspar; Engelter, Stefan T; Lyrer, Philippe; Majersik, Jennifer J; Worrall, Bradford B; Southerland, Andrew M; Markus, Hugh S; Lathrop, Mark; Thijs, Vincent N ; Leys, Didier; Amouyel, Philippe; Dallongeville, Jean; Dichgans, Martin; Pezzini, Alessandro; Bersano, Anna; Sargurupremraj, Muralidharan; Debette, Stéphanie |
| 38 | 1-Aug-2018 | Genetic literacy series: genetic epilepsy with febrile seizures plus. | Myers, Kenneth A; Scheffer, Ingrid E ; Berkovic, Samuel F |
| 39 | Feb-2019 | Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226). | Traylor, Matthew; Tozer, Daniel J; Croall, Iain D; Lisiecka Ford, Danuta M; Olorunda, Abiodun Olubunmi; Boncoraglio, Giorgio; Dichgans, Martin; Lemmens, Robin; Rosand, Jonathan; Rost, Natalia S; Rothwell, Peter M; Sudlow, Cathie L M; Thijs, Vincent N ; Rutten-Jacobs, Loes; Markus, Hugh S |
| 40 | 2019 | Genetically Determined Risk of Depression and Functional Outcome After Ischemic Stroke. | Gill, Dipender; James, Nicole E; Monori, Grace; Lorentzen, Erik; Fernandez-Cadenas, Israel; Lemmens, Robin; Thijs, Vincent N ; Rost, Natalia S; Scott, Rodney; Hankey, Graeme J; Lindgren, Arne; Jern, Christina; Maguire, Jane M |
