Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia
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
Published in Molecular psychiatry (01.08.2011)
Published in Molecular psychiatry (01.08.2011)
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A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French-Canadian population
Martin, C., Meloche, C., Rioux, M.-F., Nguyen, D.K., Carmant, L., Andermann, E., Gravel, M., Cossette, P.
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Published in Clinical genetics (01.12.2014)
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TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia
Paradis, C., Cadieux-Dion, M., Meloche, C., Gravel, M., Paradis, J., Des Roches, A., Leclerc, G., Cossette, P., Begin, P.
Published in Journal of clinical immunology (01.01.2019)
Published in Journal of clinical immunology (01.01.2019)
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Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease
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
Published in Clinical genetics (01.06.2013)
Published in Clinical genetics (01.06.2013)
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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
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
Published in Journal of paleontology (01.11.2020)
Published in Journal of paleontology (01.11.2020)
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Clinical significance of isolated hippocampal volume asymmetry in childhood epilepsy
Major, P, Décarie, J-C, Nadeau, A, Diadori, P, Lortie, A, Nguyen, D, Cossette, P, Carmant, L
Published in Neurology (26.10.2004)
Published in Neurology (26.10.2004)
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Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis
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
Published in Human molecular genetics (01.04.2013)
Published in Human molecular genetics (01.04.2013)
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Variants in CHRNB2 and CHRNA4 Identified in Patients with Insular Epilepsy
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
Published in Canadian journal of neurological sciences (01.11.2020)
Published in Canadian journal of neurological sciences (01.11.2020)
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Mutations in the calcium-related gene IL1RAPL1 are associated with autism
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.
Published in Human molecular genetics (15.12.2008)
Published in Human molecular genetics (15.12.2008)
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B.06 Two definite sudden unexpected deaths in epilepsy in a family with a DEPDC5 mutation
Nascimento, FA, Borlot, F, Cossette, P, Minassian, B, Andrade, D
Published in Canadian journal of neurological sciences (01.06.2016)
Published in Canadian journal of neurological sciences (01.06.2016)
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