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Koko, Mahmoud ORCID: 0000-0001-9512-0184, Motelow, Joshua E ORCID: 0000-0002-4367-4182, Stanley, Kate E ORCID: 0000-0002-2861-9660, Bobbili, Dheeraj R ORCID: 0000-0002-1368-9623, Dhindsa, Ryan S ORCID: 0000-0002-8965-0813, May, Patrick ORCID: 0000-0001-8698-3770, Canadian Epilepsy Network, , Epi4K Consortium, , Epilepsy Phenome/Genome Project, , EpiPGX Consortium, et al (show 1 more authors) and EuroEPINOMICS-CoGIE Consortium, (2022) Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia, 63 (3). pp. 723-735.

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Domenighetti, Cloe, Douillard, Venceslas, Sugier, Pierre-Emmanuel, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep, May, Patrick, Bobbili, Dheeraj R, Radivojkov-Blagojevic, Milena, Lichtner, Peter et al (show 70 more authors) , Singleton, Andrew B, Hernandez, Dena G, Edsall, Connor, Gourraud, Pierre-Antoine, Mellick, George D, Zimprich, Alexander, Pirker, Walter, Rogaeva, Ekaterina, Lang, Anthony E, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugenie, Brockmann, Kathrin, Deutschlander, Angela B, Hadjigeorgiou, Georges M, Dardiotis, Efthimos, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Duga, Stefano, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Matsuo, Hirotaka, Nakayama, Akiyoshi, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Kolber, Pierre, van de Warrenburg, Bart PC, Bloem, Bastiaan R, Aasly, Jan, Toft, Mathias, Pihlstrom, Lasse, Correia Guedes, Leonor, Ferreira, Joaquim J, Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy L, Ran, Caroline, Belin, Andrea C, Puschmann, Andreas, Ygland Rodstrom, Emil, Clarke, Carl E, Morrison, Karen E, Tan, Manuela, KraincMD, Dimitri, Burbulla, Lena F, Farrer, Matt J, Kruger, Rejko, Gasser, Thomas, Sharma, Manu, Vince, Nicolas and Elbaz, Alexis (2022) The Interaction between <i>HLA-DRB1</i> and Smoking in Parkinson's Disease Revisited. MOVEMENT DISORDERS, 37 (9). pp. 1929-1937.

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May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline et al (show 88 more authors) , Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-Lopez, Rosa, Baulac, Stephanie, Marini, Carla, Thiele, Holger, Altmueller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestele, Sandrine, Terragni, Benedetta, Coombs, Ian D, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Everett, Kate, Moller, Rikke S, Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, De Jonghe, Peter, Sisodiya, Sanjay M, Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S, Trenite, Dorothee Kasteleijn-Nolst, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, Francois, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clement, Jean-Francois, Cieuta-Walti, Cecile, Sills, Graeme J ORCID: 0000-0002-3389-8713, Auce, Pauls, Francis, Ben ORCID: 0000-0002-2130-5976, Johnson, Michael R, Marson, Anthony G ORCID: 0000-0002-6861-8806, Berghuis, Bianca, Sander, Josemir W, Avbersek, Andreja, McCormack, Mark, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Krenn, Martin, Zimprich, Fritz, Peter, Sarah, Nikanorova, Marina, Kraaij, Robert, van Rooij, Jeroen, Balling, Rudi, Ikram, M Arfan, Uitterlinden, Andre G, Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby PC, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nuernberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland and Lerche, Holger (2018) Rare coding variants in genes encoding GABA_A receptors in genetic generalised epilepsies: an exome-based case-control study. LANCET NEUROLOGY, 17 (8). pp. 699-708.