Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia von Piton, A, Gauthier, J, Hamdan, F F, Lafrenière, R G, Yang, Y, Henrion, E, Laurent, S, Noreau, A, Thibodeau, P, Karemera, L, Spiegelman, D, Kuku, F, Duguay, J, Destroismaisons, L, Jolivet, P, Côté, M, Lachapelle, K, Diallo, O, Raymond, A, Marineau, C, Champagne, N, Xiong, L, Gaspar, C, Rivière, J-B, Tarabeux, J, Cossette, P, Krebs, M-O, Rapoport, J L, Addington, A, DeLisi, L E, Mottron, L, Joober, R, Fombonne, E, Drapeau, P, Rouleau, G A

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The neural substrates for the rewarding and dopamine-releasing effects of medial forebrain bundle stimulation have partially discrepant frequency responses von Cossette, M.-P., Conover, K., Shizgal, P.

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High Oestradiol Replacement Reverses Response Memory Bias in Ovariectomised Female Rats Regardless of Dopamine Levels in the Dorsal Striatum von Hussain, D., Cossette, M.-P., Brake, W. G.

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A new species of Bottosaurus (Alligatoroidea: Caimaninae) from the Black Peaks Formation (Palaeocene) of Texas indicates an early radiation of North American caimanines von Cossette, Adam P

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A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French-Canadian population von Martin, C., Meloche, C., Rioux, M.-F., Nguyen, D.K., Carmant, L., Andermann, E., Gravel, M., Cossette, P.

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TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia von Paradis, C., Cadieux-Dion, M., Meloche, C., Gravel, M., Paradis, J., Des Roches, A., Leclerc, G., Cossette, P., Begin, P.

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A Systematic Review of the Giant Alligatoroid Deinosuchus from the Campanian of North America and Its Implications for the Relationships at the Root of Crocodylia von Cossette, Adam P, Brochu, Christopher A

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Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease von Cadieux-Dion, M, Andermann, E, Lachance-Touchette, P, Ansorge, O, Meloche, C, Barnabé, A, Kuzniecky, RI, Andermann, F, Faught, E, Leonberg, S, Damiano, JA, Berkovic, SF, Rouleau, GA, Cossette, P

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The contribution of ontogenetic growth trajectories on the divergent evolution of the crocodylian skull table von Cossette, Adam P., Grass, Andy D., DeGuzman, Thomas

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A New Specimen of the Alligatoroid Bottosaurus harlani and the Early History of Character Evolution in Alligatorids von Cossette, Adam P, Brochu, Christopher A

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A new crocodylid from the middle Miocene of Kenya and the timing of crocodylian faunal change in the late Cenozoic of Africa von Cossette, Adam P, Adams, Amanda J, Drumheller, Stephanie K, Nestler, Jennifer H, Benefit, Brenda R, McCrossin, Monte L, Manthi, Frederick K, Juma, Rose Nyaboke, Brochu, Christopher A

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Research Integrity: An Exploratory Survey of Administrative Science Faculties von Cossette, Pierre

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Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis von Smith, Katherine R, Dahl, Hans-Henrik M, Canafoglia, Laura, Andermann, Eva, Damiano, John, Morbin, Michela, Bruni, Amalia C, Giaccone, Giorgio, Cossette, Patrick, Saftig, Paul, Grötzinger, Joachim, Schwake, Michael, Andermann, Frederick, Staropoli, John F, Sims, Katherine B, Mole, Sara E, Franceschetti, Silvana, Alexander, Noreen A, Cooper, Jonathan D, Chapman, Harold A, Carpenter, Stirling, Berkovic, Samuel F, Bahlo, Melanie

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Mutations in the calcium-related gene IL1RAPL1 are associated with autism von Piton, Amélie, Michaud, Jacques L., Peng, Huashan, Aradhya, Swaroop, Gauthier, Julie, Mottron, Laurent, Champagne, Nathalie, Lafrenière, Ronald G., Hamdan, Fadi F., Joober, Ridha, Fombonne, Eric, Marineau, Claude, Cossette, Patrick, Dubé, Marie-Pierre, Haghighi, Pejmun, Drapeau, Pierre, Barker, Philip A., Carbonetto, Salvatore, Rouleau, Guy A.

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Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy von Brisebois, Katéri, Lortie, Anne, Vanasse, Michel, Carmant, Lionel, Rouleau, Guy A, Verner, Andrei, Cossette, Patrick, Tian Wang, Yu, Liu, Lidong, Lu, Wei-Yang, Saint-Hilaire, Jean-Marc, Dong, Haiheng

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Variants in CHRNB2 and CHRNA4 Identified in Patients with Insular Epilepsy von Cadieux-Dion, Maxime, Meneghini, Simone, Villa, Chiara, Toffa, Dènahin Hinnoutondji, Wickstrom, Ronny, Bouthillier, Alain, Sandvik, Ulrika, Gustavsson, Bengt, Mohamed, Ismail, Cossette, Patrick, Combi, Romina, Becchetti, Andrea, Nguyen, Dang Khoa

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Insulinoma misdiagnosed as intractable epilepsy von DION, M.-H, COSSETTE, P, ST-HILAIRE, J.-M, RASIO, E, NGUYEN, D. K

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CS3.1 Genetic aspects of generalised epilepsies von Cossette, P.

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A SYSTEMATIC REVIEW OF THE GIANT ALLIGATOROID DEINOSUCHUS FROM THE CAMPANIAN OF NORTH AMERICA AND ITS IMPLICATIONS FOR THE RELATIONSHIPS AT THE ROOT OF CROCODYLIA von COSSETTE, ADAM P., BROCHU, CHRISTOPHER A.

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Clinical significance of isolated hippocampal volume asymmetry in childhood epilepsy von MAJOR, P, DECARIE, J.-C, NADEAU, A, DIADORI, P, LORTIE, A, NGUYEN, D, COSSETTE, P, CARMANT, L

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