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Number of items: 9.


Allen, Andrew S, Berkovic, Samuel F, Bridgers, Joshua, Cossette, Patrick, Dlugos, Dennis, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Heinzen, Erin L, Jiang, Yu
et al (show 104 more authors) (2017) Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (7). pp. 894-899.


Gleichgerrcht, Ezequiel, Drane, Daniel L, Keller, Simon S ORCID: 0000-0001-5247-9795, Davis, Kathryn A, Gross, Robert, Willie, Jon T, Pedersen, Nigel, de Bezenac, Christophe, Jensen, Jens, Kuzniecky, Ruben
et al (show 1 more authors) (2022) Association Between Anatomical Location of Surgically Induced Lesions and Postoperative Seizure Outcome in Temporal Lobe Epilepsy. NEUROLOGY, 98 (2). E141-E151.


Gleichgerrcht, Ezequiel, Kellermann, Tanja S, Drane, Daniel L, Keller, Simon S ORCID: 0000-0001-5247-9795, McDonald, Carrie R, Rorden, Chris, Jensen, Jens, Weber, Bernd, Davis, Kathryn A, Kuzniecky, Ruben
et al (show 1 more authors) (2021) Cortical disconnection in temporal lobe epilepsy. Epilepsy & Behavior, 123. p. 108231.


Myers, Candace T, McMahon, Jacinta M, Schneider, Amy L, Petrovski, Slave, Allen, Andrew S, Carvill, Gemma L, Zemel, Matthew, Say-Kally, Julia E, LaCroix, Amy J, Heinzen, Erin L
et al (show 34 more authors) (2016) De Novo Mutations in <i>SLC1A2</i> and <i>CACNA1A</i> Are Important Causes of Epileptic Encephalopathies. AMERICAN JOURNAL OF HUMAN GENETICS, 99 (2). pp. 287-298.


Abou-Khalil, Bassel, Afawi, Zaid, Allen, Andrew S, Bautista, Jocelyn F, Bellows, Susannah T, Berkovic, Samuel F, Bluvstein, Judith, Burgess, Rosemary, Cascino, Gregory, Cops, Elisa J
et al (show 58 more authors) (2017) Phenotypic analysis of 303 multiplex families with common epilepsies. BRAIN, 140 (8). pp. 2144-2156.


Gleichgerrcht, Ezequiel, Munsell, Brent, Keller, Simon S ORCID: 0000-0001-5247-9795, Drane, Daniel L, Jensen, Jens H, Spampinato, M Vittoria, Pedersen, Nigel P, Weber, Bernd, Kuzniecky, Ruben, McDonald, Carrie
et al (show 1 more authors) (2022) Radiological identification of temporal lobe epilepsy using artificial intelligence: a feasibility study. Brain Communications, 4 (2). fcab284-.


Mirza, Nasir, Stevelink, Remi, Taweel, Basel ORCID: 0000-0002-6157-2438, Koeleman, Bobby PC, Marson, Anthony G, Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J
et al (show 151 more authors) (2021) Using common genetic variants to find drugs for common epilepsies. Brain Communications, 3 (4). fcab287-.


Altmann, Andre ORCID: 0000-0002-9265-2393, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa ORCID: 0000-0002-9578-018X, Tolomeo, Daniele, Reynolds, Regina, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo
et al (show 88 more authors) (2018) A systems-level analysis highlights microglial activation as a modifying factor in common forms of human epilepsy. Unknown.


Altmann, Andre, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa, Tolomeo, Daniele, Reynolds, Regina H, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo
et al (show 90 more authors) (2022) A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies. Neuropathology and Applied Neurobiology, 48 (1). e12758-.

This list was generated on Sat Mar 9 21:18:36 2024 GMT.