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| | Publication Year | Title | Author(s) |
| 21 | Nov-2015 | Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy | Damiano, John A; Mullen, Saul A ; Hildebrand, Michael S ; Bellows, Susannah T; Lawrence, Kate M; Arsov, Todor; Dibbens, Leanne M; Major, Heather; Dahl, Hans-Henrik M; Mefford, Heather C; Darbro, Benjamin W; Scheffer, Ingrid E ; Berkovic, Samuel F |
| 22 | 17-Mar-2015 | CHD2 variants are a risk factor for photosensitivity in epilepsy. | Galizia, Elizabeth C; Myers, Candace T; Leu, Costin; de Kovel, Carolien G F; Afrikanova, Tatiana; Cordero-Maldonado, Maria Lorena; Martins, Teresa G; Jacmin, Maxime; Drury, Suzanne; Krishna Chinthapalli, V; Muhle, Hiltrud; Pendziwiat, Manuela; Sander, Thomas; Ruppert, Ann-Kathrin; Møller, Rikke S; Thiele, Holger; Krause, Roland; Schubert, Julian; Lehesjoki, Anna-Elina; Nürnberg, Peter; Lerche, Holger; Palotie, Aarno; Coppola, Antonietta; Striano, Salvatore; Gaudio, Luigi Del; Boustred, Christopher; Schneider, Amy L ; Lench, Nicholas; Jocic-Jakubi, Bosanka; Covanis, Athanasios; Capovilla, Giuseppe; Veggiotti, Pierangelo; Piccioli, Marta; Parisi, Pasquale; Cantonetti, Laura; Sadleir, Lynette G; Mullen, Saul A ; Berkovic, Samuel F ; Stephani, Ulrich; Helbig, Ingo; Crawford, Alexander D; Esguerra, Camila V; Kasteleijn-Nolst Trenité, Dorothee G A; Koeleman, Bobby P C; Mefford, Heather C; Scheffer, Ingrid E ; Sisodiya, Sanjay M |
| 23 | 22-Sep-2014 | Lamotrigine can be beneficial in patients with Dravet syndrome. | Dalic, Linda; Mullen, Saul A ; Roulet Perez, Eliane; Scheffer, Ingrid E |
| 24 | 31-Jan-2014 | Glucose metabolism transporters and epilepsy: only GLUT1 has an established role. | Hildebrand, Michael S ; Damiano, John Anthony; Mullen, Saul A ; Bellows, Susannah T; Oliver, Karen L; Dahl, Hans-Henrik M; Scheffer, Ingrid E ; Berkovic, Samuel F |
| 25 | 10-Jan-2014 | Does variation in NIPA2 contribute to genetic generalized epilepsy? | Hildebrand, Michael S ; Damiano, John Anthony; Mullen, Saul A ; Bellows, Susannah T; Scheffer, Ingrid E ; Berkovic, Samuel F |
| 26 | 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 | 8-Jan-2013 | Epilepsy in 2012: Advances in epilepsy shed light on key questions. | Scheffer, Ingrid E ; Mullen, Saul A |
| 8 | 1-Nov-2012 | Glucose transporter 1 deficiency in the idiopathic generalized epilepsies. | Arsov, Todor; Mullen, Saul A ; Rogers, Sue; Phillips, A Marie; Lawrence, Kate M; Damiano, John Anthony; Goldberg-Stern, Hadassa; Afawi, Zaid; Kivity, Sara; Trager, Chantal; Petrou, Steven; Berkovic, Samuel F ; Scheffer, Ingrid E |
| 9 | 25-Oct-2012 | Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency. | Arsov, Todor; Mullen, Saul A ; Damiano, John Anthony; Lawrence, Kate M; Huh, Linda L; Nolan, Melinda; Young, Helen ; Thouin, Anaïs; Dahl, Hans-Henrik M; Berkovic, Samuel F ; Crompton, Douglas E; Sadleir, Lynette G; Scheffer, Ingrid E |
| 10 | 5-May-2011 | Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6. | Arsov, Todor; Smith, Katherine R; Damiano, John Anthony; Franceschetti, Silvana; Canafoglia, Laura; Bromhead, Catherine J; Andermann, Eva; Vears, Danya F; Cossette, Patrick; Rajagopalan, Sulekha; McDougall, Alan; Sofia, Vito; Farrell, Michael; Aguglia, Umberto; Zini, Andrea; Meletti, Stefano; Morbin, Michela; Mullen, Saul A ; Andermann, Frederick; Mole, Sara E; Bahlo, Melanie; Berkovic, Samuel F |
| 11 | 23-Jun-2010 | Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency. | Mullen, Saul A ; Suls, A; De Jonghe, Peter; Berkovic, Samuel F ; Scheffer, Ingrid E |
| 12 | 10-Feb-2009 | A neurologist's guide to genome-wide association studies. | Mullen, Saul A ; Crompton, Douglas E; Carney, Patrick W ; Helbig, Ingo; Berkovic, Samuel F |
| 13 | 1-Jan-2009 | Translational research in epilepsy genetics: sodium channels in man to interneuronopathy in mouse. | Mullen, Saul A ; Scheffer, Ingrid E |
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