CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations by Verlaan, Dominique J., Laurent, Sandra B., Rochefort, Daniel L., Liquori, Christina L., Marchuk, Douglas A., Siegel, Adrian M., Rouleau, Guy A.

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Isolation and genomic structure of a human homolog of the yeast periodic tryptophan protein 2 (PWP2) gene mapping to 21q22.3 by Lafrenière, R G, Rochefort, D L, Chrétien, N, Neville, C E, Korneluk, R G, Zuo, L, Wei, Y, Lichter, J, Rouleau, G A

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Genomic structure of the human GT334 ( EHOC-1) gene mapping to 21q22.3 by Lafrenière, Ronald G., Kibar, Zoha, Rochefort, Daniel L., Fei-Yu Han, Fon, Edward A., Dubé, Marie-Pierre, Kang, Xiaolin, Baird, Stephen, Korneluk, Robert G., Rommens, Johanna M., Rouleau, Guy A.

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Development of Direction Selectivity in Mouse Cortical Neurons by Rochefort, Nathalie L., Narushima, Madoka, Grienberger, Christine, Marandi, Nima, Hill, Daniel N., Konnerth, Arthur

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Staged decline of neuronal function in vivo in an animal model of Alzheimer's disease by Grienberger, Christine, Rochefort, Nathalie L, Adelsberger, Helmuth, Henning, Horst A, Hill, Daniel N, Reichwald, Julia, Staufenbiel, Matthias, Konnerth, Arthur

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Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo by Kabashi, Edor, Lin, Li, Tradewell, Miranda L., Dion, Patrick A., Bercier, Valérie, Bourgouin, Patrick, Rochefort, Daniel, Bel Hadj, Samar, Durham, Heather D., Velde, Christine Vande, Rouleau, Guy A., Drapeau, Pierre

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Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis by Kaneb, Hannah M, Folkmann, Andrew W, Belzil, Véronique V, Jao, Li-En, Leblond, Claire S, Girard, Simon L, Daoud, Hussein, Noreau, Anne, Rochefort, Daniel, Hince, Pascale, Szuto, Anna, Levert, Annie, Vidal, Sabrina, André-Guimont, Catherine, Camu, William, Bouchard, Jean-Pierre, Dupré, Nicolas, Rouleau, Guy A, Wente, Susan R, Dion, Patrick A

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Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia by Tarabeux, J, Kebir, O, Gauthier, J, Hamdan, F F, Xiong, L, Piton, A, Spiegelman, D, Henrion, É, Millet, B, Fathalli, F, Joober, R, Rapoport, J L, DeLisi, L E, Fombonne, É, Mottron, L, Forget-Dubois, N, Boivin, M, Michaud, J L, Drapeau, P, Lafrenière, R G, Rouleau, G A, Krebs, M-O

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De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia by Gauthier, Julie, Champagne, Nathalie, Lafrenière, Ronald G., Xiong, Lan, Spiegelman, Dan, Brustein, Edna, Lapointe, Mathieu, Peng, Huashan, Côté, Mélanie, Noreau, Anne, Hamdan, Fadi F., Addington, Anjené M., Rapoport, Judith L., DeLisi, Lynn E., Krebs, Marie-Odile, Joober, Ridha, Fathalli, Ferid, Mouaffak, Fayçal, Haghighi, Ali P., Néri, Christian, Dubé, Marie-Pierre, Samuels, Mark E., Marineau, Claude, Stone, Eric A., Awadalla, Philip, Barker, Philip A., Carbonetto, Salvatore, Drapeau, Pierre, Rouleau, Guy A., the S2D Team, Housman, David E.

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Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency by Berryer, Martin H., Hamdan, Fadi F., Klitten, Laura L., Møller, Rikke S., Carmant, Lionel, Schwartzentruber, Jeremy, Patry, Lysanne, Dobrzeniecka, Sylvia, Rochefort, Daniel, Neugnot-Cerioli, Mathilde, Lacaille, Jean-Claude, Niu, Zhiyv, Eng, Christine M., Yang, Yaping, Palardy, Sylvain, Belhumeur, Céline, Rouleau, Guy A., Tommerup, Niels, Immken, LaDonna, Beauchamp, Miriam H., Patel, Gayle Simpson, Majewski, Jacek, Tarnopolsky, Mark A., Scheffzek, Klaus, Hjalgrim, Helle, Michaud, Jacques L., Di Cristo, Graziella

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De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment by Hamdan, Fadi F., Daoud, Hussein, Rochefort, Daniel, Piton, Amélie, Gauthier, Julie, Langlois, Mathieu, Foomani, Gila, Dobrzeniecka, Sylvia, Krebs, Marie-Odile, Joober, Ridha, Lafrenière, Ronald G., Lacaille, Jean-Claude, Mottron, Laurent, Drapeau, Pierre, Beauchamp, Miriam H., Phillips, Michael S., Fombonne, Eric, Rouleau, Guy A., Michaud, Jacques L.

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Exome sequencing of sporadic childhood‐onset schizophrenia suggests the contribution of X‐linked genes in males by Ambalavanan, Amirthagowri, Chaumette, Boris, Zhou, Sirui, Xie, Pingxing, He, Qin, Spiegelman, Dan, Dionne‐Laporte, Alexandre, Bourassa, Cynthia V., Therrien, Martine, Rochefort, Daniel, Xiong, Lan, Dion, Patrick A., Joober, Ridha, Rapoport, Judith L., Girard, Simon L., Rouleau, Guy A.

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A Variant in XPNPEP2 Is Associated with Angioedema Induced by Angiotensin I–Converting Enzyme Inhibitors by Duan, Qing Ling, Nikpoor, Borzoo, Dubé, Marie-Pierre, Molinaro, Giuseppe, Meijer, Inge A., Dion, Patrick, Rochefort, Daniel, Saint-Onge, Judith, Flury, Leah, Brown, Nancy J., Gainer, James V., Rouleau, Jean L., Agostoni, Angelo, Cugno, Massimo, Simon, Pierre, Clavel, Pierre, Potier, Jacky, Wehbe, Bassem, Benarbia, Seddik, Marc-Aurèle, Julien, Chanard, Jacques, Foroud, Tatiana, Adam, Albert, Rouleau, Guy A.

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Determining the Immigration Potential of Plants Colonizing Disturbed Environments: The Case of Milled Peatlands in Quebec by Campbell, Daniel R., Rochefort, Line, Lavoie, Claude

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Comprehensive inventory of true flies (Diptera) at a tropical site by Brown, Brian V, Borkent, Art, Adler, Peter H, Amorim, Dalton de Souza, Barber, Kevin, Bickel, Daniel, Boucher, Stephanie, Brooks, Scott E, Burger, John, Burington, Zelia L, Capellari, Renato S, Costa, Daniel N R, Cumming, Jeffrey M, Curler, Greg, Dick, Carl W, Epler, John H, Fisher, Eric, Gaimari, Stephen D, Gelhaus, Jon, Grimaldi, David A, Hash, John, Hauser, Martin, Hippa, Heikki, Ibáñez-Bernal, Sergio, Jaschhof, Mathias, Kameneva, Elena P, Kerr, Peter H, Korneyev, Valery, Korytkowski, Cheslavo A, Kung, Giar-Ann, Kvifte, Gunnar Mikalsen, Lonsdale, Owen, Marshall, Stephen A, Mathis, Wayne, Michelsen, Verner, Naglis, Stefan, Norrbom, Allen L, Paiero, Steven, Pape, Thomas, Pereira-Colavite, Alessandre, Pollet, Marc, Rochefort, Sabrina, Rung, Alessandra, Runyon, Justin B, Savage, Jade, Silva, Vera C, Sinclair, Bradley J, Skevington, Jeffrey H, Stireman Iii, John O, Swann, John, Thompson, F Christian, Vilkamaa, Pekka, Wheeler, Terry, Whitworth, Terry, Wong, Maria, Wood, D Monty, Woodley, Norman, Yau, Tiffany, Zavortink, Thomas J, Zumbado, Manuel A

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Recombinant Congenic Strains Derived from A/J and C57BL/6J: A Tool for Genetic Dissection of Complex Traits by Fortin, Anny, Diez, Eduardo, Rochefort, Daniel, Laroche, Line, Malo, Danielle, Rouleau, Guy A., Gros, Philippe, Skamene, Emil

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Comparison of intravenous/oral ciprofloxacin plus metronidazole versus piperacillin/tazobactam in the treatment of complicated intraabdominal infections by COHN, S. M, LIPSETT, P. A, KOWALSKY, S. F, BUCHMAN, T. G, CHEADLE, W. G, MILSOM, J. W, O'MARRO, S, YELLIN, A. E, JUNGERWIRTH, S, ROCHEFORT, E. V, HAVERSTOCK, D. C

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Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo by Kabashi, Edor, Lin, Li, Tradewell, Miranda L., Dion, Patrick A., Bercier, Valérie, Bourgouin, Patrick, Rochefort, Daniel, Hadj, Samar Bel, Durham, Heather D., Velde, Christine Vande, Rouleau, Guy A., Drapeau, Pierre

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Global arthropod beta-diversity is spatially and temporally structured by latitude by Seymour, Mathew, Roslin, Tomas, deWaard, Jeremy R, Perez, Kate H J, D'Souza, Michelle L, Ratnasingham, Sujeevan, Ashfaq, Muhammad, Levesque-Beaudin, Valerie, Blagoev, Gergin A, Bukowski, Belén, Cale, Peter, Crosbie, Denise, Decaëns, Thibaud, deWaard, Stephanie L, Ekrem, Torbjørn, El-Ansary, Hosam O, Evouna Ondo, Fidèle, Fraser, David, Geiger, Matthias F, Hajibabaei, Mehrdad, Hallwachs, Winnie, Hanisch, Priscila E, Hausmann, Axel, Heath, Mark, Hogg, Ian D, Janzen, Daniel H, Kinnaird, Margaret, Kohn, Joshua R, Larrivée, Maxim, Lees, David C, León-Règagnon, Virginia, Liddell, Michael, Lijtmaer, Darío A, Lipinskaya, Tatsiana, Locke, Sean A, Manjunath, Ramya, Martins, Dino J, Martins, Marlúcia B, Mazumdar, Santosh, McKeown, Jaclyn T A, Anderson-Teixeria, Kristina, Miller, Scott E, Milton, Megan A, Miskie, Renee, Morinière, Jérôme, Mutanen, Marko, Naik, Suresh, Nichols, Becky, Noguera, Felipe A, Novotny, Vojtech, Penev, Lyubomir, Pentinsaari, Mikko, Quinn, Jenna, Ramsay, Leah, Rochefort, Regina, Schmidt, Stefan, Smith, M Alex, Sobel, Crystal N, Somervuo, Panu, Sones, Jayme E, Staude, Hermann S, St Jaques, Brianne, Stur, Elisabeth, Telfer, Angela C, Tubaro, Pablo L, Wardlaw, Tim J, Worcester, Robyn, Yang, Zhaofu, Young, Monica R, Zemlak, Tyler, Zakharov, Evgeny V, Zlotnick, Bradley, Ovaskainen, Otso, Hebert, Paul D N

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Wind erosion and surface stability in abandoned milled peatlands by Campbell, D.R, Lavoie, C, Rochefort, L

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