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Number of items: 14.


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.


Lopez, Seymour M, Aksman, Leon M, Oxtoby, Neil P, Vos, Sjoerd B, Rao, Jun, Kaestner, Erik, Alhusaini, Saud, Alvim, Marina, Bender, Benjamin, Bernasconi, Andrea
et al (show 66 more authors) (2022) Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data. EPILEPSIA, 63 (8). pp. 2081-2095.


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-.


Larivière, Sara, Rodríguez-Cruces, Raúl, Royer, Jessica, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon S ORCID: 0000-0001-5247-9795, Cendes, Fernando, Yasuda, Clarissa, Bonilha, Leonardo
et al (show 52 more authors) (2020) Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study. Science Advances, 6 (47). eabc6457-eabc6457.


Larivière, Sara, Rodríguez-Cruces, Raúl, Royer, Jessica, Caligiuri, Maria Eugenia ORCID: 0000-0002-2030-5552, Gambardella, Antonio ORCID: 0000-0001-7384-3074, Concha, Luis, Keller, Simon ORCID: 0000-0001-5247-9795, Cendes, Fernando, Yasuda, Clarissa, Bonilha, Leonardo
et al (show 52 more authors) (2020) Network-based atrophy modelling in the common epilepsies: a worldwide ENIGMA study. Science advances.


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.


Larivière, Sara, Royer, Jessica, Rodríguez-Cruces, Raúl, Paquola, Casey, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon S ORCID: 0000-0001-5247-9795, Cendes, Fernando, Yasuda, Clarissa L
et al (show 64 more authors) (2022) Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression. Nature Communications, 13 (1). 4320-.


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.


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-.


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.


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 Tue Jan 16 06:14:03 2024 GMT.