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Number of items: 15.


Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer
et al (show 561 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313-+.


Sisodiya, Sanjay M, Whelan, Christopher D, Hatton, Sean N, Huynh, Khoa, Altmann, Andre, Ryten, Mina, Vezzani, Annamaria, Caligiuri, Maria Eugenia, Labate, Angelo, Gambardella, Antonio
et al (show 62 more authors) (2022) The ENIGMA-Epilepsy working group: Mapping disease from large data sets. HUMAN BRAIN MAPPING, 43 (1). pp. 113-128.


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.


Walton, E, Hibar, D, Yilmaz, Z, Jahanshad, N, Cheung, J, Batury, V-L, Seitz, J, Bulik, CM, Thompson, PM, Ehrlich, Stefan
et al (show 500 more authors) (2019) Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. MOLECULAR NEUROBIOLOGY, 56 (7). pp. 5146-5156.


Satizabal, Claudia L, Adams, Hieab HH, Hibar, Derrek P, White, Charles C, Knol, Maria J, Stein, Jason L, Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V
et al (show 279 more authors) (2019) Genetic architecture of subcortical brain structures in 38,851 individuals. NATURE GENETICS, 51 (11). 1624-+.


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.


Hibar, Derrek P, Adams, Hieab HH, Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L, Hofer, Edith, Renteria, Miguel E, Bis, Joshua C, Arias-Vasquez, Alejandro, Ikram, M Kamran
et al (show 322 more authors) (2017) Novel genetic loci associated with hippocampal volume. NATURE COMMUNICATIONS, 8 (1). 13624-.


Whelan, Christopher D, Altmann,, Andre, Botia, Juan A, Jahanshad, Neda, Hibar, Derrek P, Absil, Julie, Alhusaini, Saud, Alvim, Marina KM, Auvinen, Pia, Bartolini, Emanuele
et al (show 2 more authors) (2018) Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study. Brain, 141 (2). pp. 391-408.


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.


Grasby, Katrina L, Jahanshad, Neda, Painter, Jodie N, Colodro-Conde, Lucia, Bralten, Janita, Hibar, Derrek P, Lind, Penelope A, Pizzagalli, Fabrizio, Ching, Christopher RK, McMahon, Mary Agnes B
et al (show 350 more authors) (2020) The genetic architecture of the human cerebral cortex. SCIENCE, 367 (6484). 1340-+.


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 Wed Feb 7 20:36:44 2024 GMT.