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Number of items: 15.


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, Munsell, Brent C, Alhusaini, Saud, Alvim, Marina KM, Bargalló, Núria, Bender, Benjamin, Bernasconi, Andrea, Bernasconi, Neda, Bernhardt, Boris, Blackmon, Karen
et al (show 56 more authors) (2021) Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: a worldwide ENIGMA-Epilepsy study. NeuroImage: Clinical, 31. p. 102765.


Wolking, Stefan, Moreau, Claudia, McCormack, Mark, Krause, Roland, Krenn, Martin, Berkovic, Samuel, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Johnson, Michael R
et al (show 14 more authors) (2021) Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy. ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 8 (7). pp. 1376-1387.


Silvennoinen, Katri, de Lange, Nikola, Zagaglia, Sara, Balestrini, Simona, Androsova, Ganna, Wassenaar, Merel, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Berghuis, Bianca
et al (show 21 more authors) (2019) Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy. EPILEPSIA OPEN, 4 (3). pp. 420-430.


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.


Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L, Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Bruenger, Tobias, Thomas, Rhys H
et al (show 313 more authors) (2023) Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals. NATURE COMMUNICATIONS, 14 (1). 4392-.


Kerestes, Rebecca ORCID: 0000-0003-1298-9904, Perry, Andrew, Vivash, Lucy ORCID: 0000-0002-1182-0907, O'Brien, Terence J ORCID: 0000-0002-7198-8621, Alvim, Marina KM ORCID: 0000-0002-6780-0761, Arienzo, Donatello, Aventurato, Ítalo K, Ballerini, Alice ORCID: 0000-0002-0544-1599, Baltazar, Gabriel F, Bargalló, Núria
et al (show 55 more authors) (2023) Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study. [Preprint]


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.


Boothman, Isabelle, Clayton, Lisa M, Mccormack, Mark, Driscoll, Alexandra McKibben, Stevelink, Remi, Moloney, Patrick, Krause, Roland, Kunz, Wolfram S, Diehl, Sarah, O'Brien, Terence J
et al (show 17 more authors) (2023) Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin. FRONTIERS IN NEUROSCIENCE, 17. 1156362-.


Park, Bo-yong, Lariviere, Sara, Rodriguez-Cruces, Raul, Royer, Jessica, Tavakol, Shahin, Wang, Yezhou, Caciagli, Lorenzo, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis
et al (show 77 more authors) (2022) Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy. BRAIN, 145 (4). pp. 1285-1298.


von Wrede, Randi, Witt, Juri-Alexander, Auvin, Stephane, Devlin, Anita, Lagae, Lieven, Marson, Anthony ORCID: 0000-0002-6861-8806, Meador, Kimford J, O'Brien, Terence J, Park, Jun, Surges, Rainer
et al (show 3 more authors) (2023) Unjustified allegation on cancer risks in children of mothers with epilepsy taking high-dose folic acid during pregnancy-No proof of a causal relationship. EPILEPSIA, 64 (9). pp. 2239-2243.


Hatton, Sean N, Huynh, Khoa H, Bonilha, Leonardo, Abela, Eugenio, Alhusaini, Saud, Altmann, Andre, Alvim, Marina KM, Balachandra, Akshara R, Bartolini, Emanuele, Bender, Benjamin
et al (show 66 more authors) (2020) White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study. Brain, 143 (8). pp. 2454-2473.


Hatton, Sean N ORCID: 0000-0002-9149-8726, Huynh, Khoa H, Bonilha, Leonardo, Abela, Eugenio ORCID: 0000-0002-9356-1450, Alhusaini, Saud, Altmann, Andre ORCID: 0000-0002-9265-2393, Alvim, Marina KM, Balachandra, Akshara R, Bartolini, Emanuele, Bender, Benjamin
et al (show 66 more authors) (2020) White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study. Brain : a journal of neurology, 143 (8). 2454 - 2473.


Berghuis, Bianca, Stapleton, Caragh, Sonsma, Anja CM, Hulst, Janic, de Haan, Gerrit-Jan, Lindhout, Dick, Demurtas, Rita, EpiPGX Consortium, , Krause, Roland, Depondt, Chantal
et al (show 17 more authors) (2019) A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Epilepsia Open, 4 (1). pp. 102-109.


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 Mon Feb 12 05:49:46 2024 GMT.