Novel de novo SHANK3 mutation in autistic patients von Gauthier, Julie, Spiegelman, Dan, Piton, Amélie, Lafrenière, Ronald G., Laurent, Sandra, St-Onge, Judith, Lapointe, Line, Hamdan, Fadi F., Cossette, Patrick, Mottron, Laurent, Fombonne, Éric, Joober, Ridha, Marineau, Claude, Drapeau, Pierre, Rouleau, Guy A.

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De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy von Hamdan, Fadi F., Piton, Amélie, Gauthier, Julie, Lortie, Anne, Dubeau, François, Dobrzeniecka, Sylvia, Spiegelman, Dan, Noreau, Anne, Pellerin, Stéphanie, Côté, Mélanie, Henrion, Edouard, Fombonne, Éric, Mottron, Laurent, Marineau, Claude, Drapeau, Pierre, Lafrenière, Ronald G., Lacaille, Jean Claude, Rouleau, Guy A., Michaud, Jacques L.

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Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 von Rouleau, Guy A, Merel, Philippe, Lutchman, Mohini, Sanson, Marc, Zucman, Jessica, Marineau, Claude, Hoang-Xuan, Khé, Demczuk, Suzanne, Desmaze, Chantal, Plougastel, Béatrice, Pulst, Stefan M, Lenoir, Gilbert, Bijlsma, Emilia, Fashold, Raimund, Dumanski, Jan, Jong, Pieter de, Parry, Dilys, Eldrige, Roswell, Aurias, Alain, Delattre, Olivier, Thomas, Gilles

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Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability von Hamdan, Fadi F., Gauthier, Julie, Araki, Yoichi, Lin, Da-Ting, Yoshizawa, Yuhki, Higashi, Kyohei, Park, A-Reum, Spiegelman, Dan, Dobrzeniecka, Sylvia, Piton, Amélie, Tomitori, Hideyuki, Daoud, Hussein, Massicotte, Christine, Henrion, Edouard, Diallo, Ousmane, Shekarabi, Masoud, Marineau, Claude, Shevell, Michael, Maranda, Bruno, Mitchell, Grant, Nadeau, Amélie, D'Anjou, Guy, Vanasse, Michel, Srour, Myriam, Lafrenière, Ronald G., Drapeau, Pierre, Lacaille, Jean Claude, Kim, Eunjoon, Lee, Jae-Ran, Igarashi, Kazuei, Huganir, Richard L., Rouleau, Guy A., Michaud, Jacques L.

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Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation von Hamdan, Fadi F, Gauthier, Julie, Spiegelman, Dan, Noreau, Anne, Yang, Yan, Pellerin, Stéphanie, Dobrzeniecka, Sylvia, Côté, Mélanie, Perreau-Linck, Elizabeth, Carmant, Lionel, D'Anjou, Guy, Fombonne, Éric, Addington, Anjene M, Rapoport, Judith L, Delisi, Lynn E, Krebs, Marie-Odile, Mouaffak, Faycal, Joober, Ridha, Mottron, Laurent, Drapeau, Pierre, Marineau, Claude, Lafrenière, Ronald G, Lacaille, Jean Claude, Rouleau, Guy A, Michaud, Jacques L

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Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia von 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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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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Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts von Awadalla, Philip, Gauthier, Julie, Myers, Rachel A., Casals, Ferran, Hamdan, Fadi F., Griffing, Alexander R., Côté, Mélanie, Henrion, Edouard, Spiegelman, Dan, Tarabeux, Julien, Piton, Amélie, Yang, Yan, Boyko, Adam, Bustamante, Carlos, Xiong, Lan, Rapoport, Judith L., Addington, Anjené M., DeLisi, J. Lynn E., Krebs, Marie-Odile, Joober, Ridha, Millet, Bruno, Fombonne, Éric, Mottron, Laurent, Zilversmit, Martine, Keebler, Jon, Daoud, Hussein, Marineau, Claude, Roy-Gagnon, Marie-Hélène, Dubé, Marie-Pierre, Eyre-Walker, Adam, Drapeau, Pierre, Stone, Eric A., Lafrenière, Ronald G., Rouleau, Guy A.

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Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability von Hamdan, Fadi F., Gauthier, Julie, Araki, Yoichi, Lin, Da-Ting, Yoshizawa, Yuhki, Higashi, Kyohei, Park, A-reum, Spiegelman, Dan, Dobrzeniecka, Sylvia, Piton, Amélie, Tomitori, Hideyuki, Daoud, Hussein, Massicotte, Christine, Henrion, Edouard, Diallo, Ousmane, Shekarabi, Masoud, Marineau, Claude, Shevell, Michael, Maranda, Bruno, Mitchell, Grant, Nadeau, Amélie, D'Anjou, Guy, Vanasse, Michel, Srour, Myriam, Lafrenière, Ronald G., Drapeau, Pierre, Lacaille, Jean Claude, Kim, Eunjoon, Lee, Jae-Ran, Igarashi, Kazuei, Huganir, Richard L., Rouleau, Guy A., Michaud, Jacques L.

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Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental RetardationBrief Report von Hamdan, Fadi F, Gauthier, Julie, Spiegelman, Dan, Noreau, Anne, Yang, Yan, Pellerin, Stéphanie, Dobrzeniecka, Sylvia, Côté, Mélanie, Perreau-Linck, Elizabeth, Carmant, Lionel, D'Anjou, Guy, Fombonne, Éric, Addington, Anjene M, Rapoport, Judith L, Delisi, Lynn E, Krebs, Marie-Odile, Mouaffak, Faycal, Joober, Ridha, Mottron, Laurent, Drapeau, Pierre, Marineau, Claude, Lafrenière, Ronald G, Lacaille, Jean Claude, Rouleau, Guy A, Michaud, Jacques L

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novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia von 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

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Molecular cloning and analysis of cDNA encoding a plant tryptophan decarboxylase: comparison with animal dopa decarboxylases von De Luca, V, Marineau, C, Brisson, N

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The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q von CASAUBON, L. K, MELANSON, M, ROULEAU, G. A, LOPES-CENDES, I, MARINEAU, C, ANDERMANN, E, ANDERMANN, F, WEISSENBACH, J, PREVOST, C, BOUCHARD, J.-P, MATHIEU, J

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Novel De Novo SHANK3 Mutation in Autistic Patients von GAUTHIER, Julie, SPIEGELMAN, Dan, FOMBONNE, Eric, JOOBER, Ridha, MARINEAU, Claude, DRAPEAU, Pierre, ROULEAU, Guy A, PITON, Amélie, LAFRENIERE, Ronald G, LAURENT, Sandra, ST-ONGE, Judith, LAPOINTE, Line, HAMDAN, Fadi F, COSSETTE, Patrick, MOTTRON, Laurent

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Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus von Sanson, Marc, Marineau, Claude, Desmaze, Chantale, Lutchman, Mohini, Ruttledge, Martin, Baron, Chantal, Narod, Steven, Delattre, Olivier, Lenoir, Gilbert, Thomas, Gilles, Aurlas, Alain, Rouleau, Guy A.

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The mouse homologue of the neurofibromatosis type 2 gene is highly conserved von O.Claudio, Jaime, Marineau, Claude, A.Rouleau, Guy

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Dinucleotide repeat polymorphism at the D22S268 locus von Marineau, Claude, Baron, Chantal, Delattre, Olivier, Zucman, Jessica, Thomas, Gilles, Rouleau, Guy A.

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Dinucleotide repeat polymorphism at the human CRYB2 gene locus (22q11.2) von Marineau, Claude, Rouleau, Guy A.

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Dinucleotide repeat polymorphism at the D22S264 locus von Marineau, Claude, Aubry, Muriel, Julien, Jean-Pierre, Rouleau, Guy A.

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METHODS OF STRATIFYING, PROGNOSING AND DIAGNOSING SCHIZOPHRENIA, MUTANT NUCLEIC ACID MOLECULES AND POLYPEPTIDES von GAUTHIER, MARTINE, ROULEAU, GUY, A, DRAPEAU, PIERRE, MARINEAU, CLAUDE

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