Operative list of genes associated with autism and neurodevelopmental disorders based on database review von Leblond, Claire S., Le, Thuy-Linh, Malesys, Simon, Cliquet, Freddy, Tabet, Anne-Claude, Delorme, Richard, Rolland, Thomas, Bourgeron, Thomas

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SMPD1 mutations, activity, and α‐synuclein accumulation in Parkinson's disease von Alcalay, Roy N., Mallett, Victoria, Vanderperre, Benoît, Tavassoly, Omid, Dauvilliers, Yves, Wu, Richard Y.J., Ruskey, Jennifer A., Leblond, Claire S., Ambalavanan, Amirthagowri, Laurent, Sandra B., Spiegelman, Dan, Dionne‐Laporte, Alexandre, Liong, Christopher, Levy, Oren A., Fahn, Stanley, Waters, Cheryl, Kuo, Sheng‐Han, Chung, Wendy K., Ford, Blair, Marder, Karen S., Kang, Un Jung, Hassin‐Baer, Sharon, Greenbaum, Lior, Trempe, Jean‐Francois, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Clark, Lorraine N., Langlois, Melanie, Dion, Patrick A., Fon, Edward A., Dupre, Nicolas, Rouleau, Guy A., Gan‐Or, Ziv

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Dissection of genetic factors associated with amyotrophic lateral sclerosis von Leblond, Claire S., Kaneb, Hannah M., Dion, Patrick A., Rouleau, Guy A.

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Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism von Pretzsch, Charlotte M., Floris, Dorothea L., Schäfer, Tim, Bletsch, Anke, Gurr, Caroline, Lombardo, Michael V., Chatham, Chris H., Tillmann, Julian, Charman, Tony, Arenella, Martina, Jones, Emily, Ambrosino, Sara, Bourgeron, Thomas, Dumas, Guillaume, Cliquet, Freddy, Leblond, Claire S., Loth, Eva, Oakley, Bethany, Buitelaar, Jan K., Baron-Cohen, Simon, Beckmann, Christian F., Persico, Antonio M., Banaschewski, Tobias, Durston, Sarah, Freitag, Christine M., Murphy, Declan G. M., Ecker, Christine

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SHANK1 Deletions in Males with Autism Spectrum Disorder von Sato, Daisuke, Lionel, Anath C., Leblond, Claire S., Prasad, Aparna, Pinto, Dalila, Walker, Susan, O'Connor, Irene, Russell, Carolyn, Drmic, Irene E., Hamdan, Fadi F., Michaud, Jacques L., Endris, Volker, Roeth, Ralph, Delorme, Richard, Huguet, Guillaume, Leboyer, Marion, Rastam, Maria, Gillberg, Christopher, Lathrop, Mark, Stavropoulos, Dimitri J., Anagnostou, Evdokia, Weksberg, Rosanna, Fombonne, Eric, Zwaigenbaum, Lonnie, Fernandez, Bridget A., Roberts, Wendy, Rappold, Gudrun A., Marshall, Christian R., Bourgeron, Thomas, Szatmari, Peter, Scherer, Stephen W.

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Heritability of the melatonin synthesis variability in autism spectrum disorders von Benabou, Marion, Rolland, Thomas, Leblond, Claire S., Millot, Gaël A., Huguet, Guillaume, Delorme, Richard, Leboyer, Marion, Pagan, Cécile, Callebert, Jacques, Maronde, Erik, Bourgeron, Thomas

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The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations von Ey, Elodie, Torquet, Nicolas, Le Sourd, Anne-Marie, Leblond, Claire S., Boeckers, Tobias M., Faure, Philippe, Bourgeron, Thomas

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Stratifying the autistic phenotype using electrophysiological indices of social perception von Mason, L, Moessnang, C, Chatham, C, Ham, L, Tillmann, J, Dumas, G, Ellis, C, Leblond, CS, Cliquet, F, Bourgeron, T

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Neurobiological Correlates of Change in Adaptive Behavior in Autism von Pretzsch, Charlotte M, Schäfer, Tim, Lombardo, Michael V, Warrier, Varun, Mann, Caroline, Bletsch, Anke, Chatham, Chris H, Floris, Dorothea L, Tillmann, Julian, Yousaf, Afsheen, Jones, Emily, Charman, Tony, Ambrosino, Sara, Bourgeron, Thomas, Dumas, Guillaume, Loth, Eva, Oakley, Bethany, Buitelaar, Jan K, Cliquet, Freddy, Leblond, Claire S, Baron-Cohen, Simon, Beckmann, Christian F, Banaschewski, Tobias, Durston, Sarah, Freitag, Christine M, Murphy, Declan G.M, Ecker, Christine

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Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis von 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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Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2 von Schmeisser, Michael J., Ey, Elodie, Wegener, Stephanie, Bockmann, Juergen, Stempel, A. Vanessa, Kuebler, Angelika, Janssen, Anna-Lena, Udvardi, Patrick T., Shiban, Ehab, Spilker, Christina, Balschun, Detlef, Skryabin, Boris V., Dieck, Susanne tom, Smalla, Karl-Heinz, Montag, Dirk, Leblond, Claire S., Faure, Philippe, Torquet, Nicolas, Le Sourd, Anne-Marie, Toro, Roberto, Grabrucker, Andreas M., Shoichet, Sarah A., Schmitz, Dietmar, Kreutz, Michael R., Bourgeron, Thomas, Gundelfinger, Eckart D., Boeckers, Tobias M.

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Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease von Ross, Jay P, Dupre, Nicolas, Dauvilliers, Yves, Strong, Stephanie, Ambalavanan, Amirthagowri, Spiegelman, Dan, Dionne-Laporte, Alexandre, Pourcher, Emanuelle, Langlois, Melanie, Boivin, Michel, Leblond, Claire S, Dion, Patrick A, Rouleau, Guy A, Gan-Or, Ziv

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Behavioral profiles of mouse models for autism spectrum disorders von Ey, Elodie, Leblond, Claire S., Bourgeron, Thomas

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Phenotypic effects of genetic variants associated with autism von Rolland, Thomas, Cliquet, Freddy, Anney, Richard J. L., Moreau, Clara, Traut, Nicolas, Mathieu, Alexandre, Huguet, Guillaume, Duan, Jinjie, Warrier, Varun, Portalier, Swan, Dry, Louise, Leblond, Claire S., Douard, Elise, Amsellem, Frédérique, Malesys, Simon, Maruani, Anna, Toro, Roberto, Børglum, Anders D., Grove, Jakob, Baron-Cohen, Simon, Packer, Alan, Chung, Wendy K., Jacquemont, Sébastien, Delorme, Richard, Bourgeron, Thomas

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A Genetic Bridge Between Medicine and Neurodiversity for Autism von Leblond, Claire S, Rolland, Thomas, Barthome, Eli, Mougin, Zakaria, Fleury, Mathis, Ecker, Christine, Bonnot-Briey, Stéf, Cliquet, Freddy, Tabet, Anne-Claude, Maruani, Anna, Chaumette, Boris, Green, Jonathan, Delorme, Richard, Bourgeron, Thomas

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Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome von Vitrac, Aline, Leblond, Claire S., Rolland, Thomas, Cliquet, Freddy, Mathieu, Alexandre, Maruani, Anna, Delorme, Richard, Schön, Michael, Grabrucker, Andreas M., van Ravenswaaij-Arts, Conny, Phelan, Katy, Tabet, Anne-Claude, Bourgeron, Thomas

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Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients von Gonzalez-Perez, Paloma, Woehlbier, Ute, Chian, Ru-Ju, Sapp, Peter, Rouleau, Guy A., Leblond, Claire S., Daoud, Hussein, Dion, Patrick A., Landers, John E., Hetz, Claudio, Brown, Robert H.

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Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder von Li, Jiao, Ruskey, Jennifer A., Arnulf, Isabelle, Dauvilliers, Yves, Hu, Michele T.M., Högl, Birgit, Leblond, Claire S., Zhou, Sirui, Ambalavanan, Amirthagowri, Ross, Jay P., Bourassa, Cynthia V., Spiegelman, Dan, Laurent, Sandra B, Stefani, Ambra, Charley Monaca, Christelle, Cochen De Cock, Valérie, Boivin, Michel, Ferini‐Strambi, Luigi, Plazzi, Giuseppe, Antelmi, Elena, Young, Peter, Heidbreder, Anna, Labbe, Catherine, Ferman, Tanis J., Dion, Patrick A., Fan, Dongsheng, Desautels, Alex, Gagnon, Jean‐François, Dupré, Nicolas, Fon, Edward A., Montplaisir, Jacques Y., Boeve, Bradley F., Postuma, Ronald B., Rouleau, Guy A., Ross, Owen A., Gan‐Or, Ziv

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Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis von Leblond, Claire S, Gan-Or, Ziv, Spiegelman, Dan, Laurent, Sandra B, Szuto, Anna, Hodgkinson, Alan, Dionne-Laporte, Alexandre, Provencher, Pierre, de Carvalho, Mamede, Orrù, Sandro, Brunet, Denis, Bouchard, Jean-Pierre, Awadalla, Philip, Dupré, Nicolas, Dion, Patrick A, Rouleau, Guy A

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Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations von Gouder, Laura, Vitrac, Aline, Goubran-Botros, Hany, Danckaert, Anne, Tinevez, Jean-Yves, André-Leroux, Gwenaëlle, Atanasova, Ekaterina, Lemière, Nathalie, Biton, Anne, Leblond, Claire S., Poulet, Aurélie, Boland, Anne, Deleuze, Jean-François, Benchoua, Alexandra, Delorme, Richard, Bourgeron, Thomas, Cloëz-Tayarani, Isabelle

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