Analysis of Three Deletion Breakpoints in Xp21.1 and the Further Localization of RP3 by Brown, John, Dry, Katherine L., Edgar, Alexander J., Pryde, Fiona E., Hardwick, Lee J., Aldred, Micheala A., Lester, Douglas H., Boyle, Shelagh, Kaplan, Josseline, Dufier, Jean-Louis, Ho, Meng-Fatt, Monaco, Anthony M., Musarella, Maria A., Wright, Alan F.

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Common variants in left/right asymmetry genes and pathways are associated with relative hand skill by Brandler, William M, Morris, Andrew P, Evans, David M, Scerri, Thomas S, Kemp, John P, Timpson, Nicholas J, St Pourcain, Beate, Smith, George Davey, Ring, Susan M, Stein, John, Monaco, Anthony P, Talcott, Joel B, Fisher, Simon E, Webber, Caleb, Paracchini, Silvia

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Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments by Leblond, Claire S, Nava, Caroline, Polge, Anne, Gauthier, Julie, Huguet, Guillaume, Lumbroso, Serge, Giuliano, Fabienne, Stordeur, Coline, Depienne, Christel, Mouzat, Kevin, Pinto, Dalila, Howe, Jennifer, Lemière, Nathalie, Durand, Christelle M, Guibert, Jessica, Ey, Elodie, Toro, Roberto, Peyre, Hugo, Mathieu, Alexandre, Amsellem, Frédérique, Rastam, Maria, Gillberg, I Carina, Rappold, Gudrun A, Holt, Richard, Monaco, Anthony P, Maestrini, Elena, Galan, Pilar, Heron, Delphine, Jacquette, Aurélia, Afenjar, Alexandra, Rastetter, Agnès, Brice, Alexis, Devillard, Françoise, Assouline, Brigitte, Laffargue, Fanny, Lespinasse, James, Chiesa, Jean, Rivier, François, Bonneau, Dominique, Regnault, Beatrice, Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Sanlaville, Damien, Schluth-Bolard, Caroline, Edery, Patrick, Perrin, Laurence, Tabet, Anne Claude, Schmeisser, Michael J, Boeckers, Tobias M, Coleman, Mary, Sato, Daisuke, Szatmari, Peter, Scherer, Stephen W, Rouleau, Guy A, Betancur, Catalina, Leboyer, Marion, Gillberg, Christopher, Delorme, Richard, Bourgeron, Thomas

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Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility by Yeshaw, Wondwossen M, van der Zwaag, Marianne, Pinto, Francesco, Lahaye, Liza L, Faber, Anita Ie, Gómez-Sánchez, Rubén, Dolga, Amalia M, Poland, Conor, Monaco, Anthony P, van IJzendoorn, Sven Cd, Grzeschik, Nicola A, Velayos-Baeza, Antonio, Sibon, Ody Cm

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Impact of Fine Particulate Matter (PM2.5) Exposure During Wildfires on Cardiovascular Health Outcomes by Haikerwal, Anjali, Akram, Muhammad, Del Monaco, Anthony, Smith, Karen, Sim, Malcolm R, Meyer, Mick, Tonkin, Andrew M, Abramson, Michael J, Dennekamp, Martine

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Environmental enrichment promotes robust functional and histological benefits in female rats after controlled cortical impact injury by Monaco, Christina M., Mattiola, Vincent V., Folweiler, Kaitlin A., Tay, Justin K., Yelleswarapu, Narayana K., Curatolo, Lauren M., Matter, Ashley M., Cheng, Jeffrey P., Kline, Anthony E.

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Molecular evolution of FOXP2, a gene involved in speech and language by Enard, Wolfgang, Przeworski, Molly, Fisher, Simon E., Lai, Cecilia S. L., Wiebe, Victor, Kitano, Takashi, Monaco, Anthony P., Pääbo, Svante

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Forest Fire Smoke Exposures and Out-of-Hospital Cardiac Arrests in Melbourne, Australia: A Case-Crossover Study by Dennekamp, Martine, Straney, Lahn D, Erbas, Bircan, Abramson, Michael J, Keywood, Melita, Smith, Karen, Sim, Malcolm R, Glass, Deborah C, Del Monaco, Anthony, Haikerwal, Anjali, Tonkin, Andrew M

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Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits by MacDermot, Kay D., Bonora, Elena, Sykes, Nuala, Coupe, Anne-Marie, Lai, Cecilia S.L., Vernes, Sonja C., Vargha-Khadem, Faraneh, McKenzie, Fiona, Smith, Robert L., Monaco, Anthony P., Fisher, Simon E.

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CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment by Newbury, Dianne F., Winchester, Laura, Addis, Laura, Paracchini, Silvia, Buckingham, Lyn-Louise, Clark, Ann, Cohen, Wendy, Cowie, Hilary, Dworzynski, Katharina, Everitt, Andrea, Goodyer, Ian M., Hennessy, Elizabeth, Kindley, A. David, Miller, Laura L., Nasir, Jamal, O'Hare, Anne, Shaw, Duncan, Simkin, Zoe, Simonoff, Emily, Slonims, Vicky, Watson, Jocelynne, Ragoussis, Jiannis, Fisher, Simon E., Seckl, Jonathon R., Helms, Peter J., Bolton, Patrick F., Pickles, Andrew, Conti-Ramsden, Gina, Baird, Gillian, Bishop, Dorothy V.M., Monaco, Anthony P.

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The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on by Guidi, Luiz G., Velayos‐Baeza, Antonio, Martinez‐Garay, Isabel, Monaco, Anthony P., Paracchini, Silvia, Bishop, Dorothy V. M., Molnár, Zoltán

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Functional impact of global rare copy number variation in autism spectrum disorders by Anney, Richard, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R., Almeida, Joana, Berney, Tom, Bölte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Bryson, Susan E., Carson, Andrew R., Casey, Jillian, Crawford, Emily L., Cytrynbaum, Cheryl, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Freitag, Christine M., Gilbert, John, Glessner, Joseph T., Goldberg, Jeremy, Green, Andrew, Green, Jonathan, Guter, Stephen J., Heron, Elizabeth A., Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Klauck, Sabine M., Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Le Couteur, Ann, Leventhal, Bennett L., Lord, Catherine, Maestrini, Elena, Mahoney, William, McConachie, Helen, McDougle, Christopher J., Merikangas, Alison, Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Noor, Abdul, Nygren, Gudrun, Papanikolaou, Katerina, Parrini, Barbara, Paton, Tara, Piven, Joseph, Ponting, Chris P., Roberts, Wendy, Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Senman, Lili, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Stein, Olaf, Sykes, Nuala, Stoppioni, Vera, Strawbridge, Christina, Thompson, Ann P., Tsiantis, John, Van Engeland, Herman, Volkmar, Fred, Wallace, Simon, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Webber, Caleb, Weksberg, Rosanna, Wood, Shawn, Wu, Jing, Yaspan, Brian L., Zwaigenbaum, Lonnie, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Cuccaro, Michael L., Devlin, Bernie, Ennis, Sean, Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Miller, Judith, Monaco, Anthony P., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica J., Scherer, Stephen W., Sutcliffe, James S., Betancur, Catalina

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Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia by Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Brandler, William, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd

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Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders by Leblond, Claire S, Heinrich, Jutta, Delorme, Richard, Proepper, Christian, Betancur, Catalina, Huguet, Guillaume, Konyukh, Marina, Chaste, Pauline, Ey, Elodie, Rastam, Maria, Anckarsäter, Henrik, Nygren, Gudrun, Gillberg, I Carina, Melke, Jonas, Toro, Roberto, Regnault, Beatrice, Fauchereau, Fabien, Mercati, Oriane, Lemière, Nathalie, Skuse, David, Poot, Martin, Holt, Richard, Monaco, Anthony P, Järvelä, Irma, Kantojärvi, Katri, Vanhala, Raija, Curran, Sarah, Collier, David A, Bolton, Patrick, Chiocchetti, Andreas, Klauck, Sabine M, Poustka, Fritz, Freitag, Christine M, Waltes, Regina, Kopp, Marnie, Duketis, Eftichia, Bacchelli, Elena, Minopoli, Fiorella, Ruta, Liliana, Battaglia, Agatino, Mazzone, Luigi, Maestrini, Elena, Sequeira, Ana F, Oliveira, Barbara, Vicente, Astrid, Oliveira, Guiomar, Pinto, Dalila, Scherer, Stephen W, Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Bonneau, Dominique, Guinchat, Vincent, Devillard, Françoise, Assouline, Brigitte, Mouren, Marie-Christine, Leboyer, Marion, Gillberg, Christopher, Boeckers, Tobias M, Bourgeron, Thomas

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DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits by Scerri, Tom S, Morris, Andrew P, Buckingham, Lyn-Louise, Newbury, Dianne F, Miller, Laura L, Monaco, Anthony P, Bishop, Dorothy V.M, Paracchini, Silvia

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Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia by Pagnamenta, Alistair T, Bacchelli, Elena, de Jonge, Maretha V, Mirza, Ghazala, Scerri, Thomas S, Minopoli, Fiorella, Chiocchetti, Andreas, Ludwig, Kerstin U, Hoffmann, Per, Paracchini, Silvia, Lowy, Ernesto, Harold, Denise H, Chapman, Jade A, Klauck, Sabine M, Poustka, Fritz, Houben, Renske H, Staal, Wouter G, Ophoff, Roel A, O'Donovan, Michael C, Williams, Julie, Nöthen, Markus M, Schulte-Körne, Gerd, Deloukas, Panos, Ragoussis, Jiannis, Bailey, Anthony J, Maestrini, Elena, Monaco, Anthony P

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Multiple courses of antenatal corticosteroids for preterm birth (MACS): a randomised controlled trial by Murphy, Kellie E, Dr, Hannah, Mary E, Prof, Willan, Andrew R, Prof, Hewson, Sheila A, BA, Ohlsson, Arne, Prof, Kelly, Edmond N, MB, Matthews, Stephen G, Prof, Saigal, Saroj, Prof, Asztalos, Elizabeth, MD, Ross, Susan, Prof, Delisle, Marie-France, MD, Amankwah, Kofi, Prof, Guselle, Patricia, MSc, Gafni, Amiram, Prof, Lee, Shoo K, Prof, Armson, B Anthony, Prof

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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia by The Psychiatric Genomics Consortium, The Autism Spectrum Disorders Working Group Of, Anney, Richard J L, Ripke, Stephan, Anttila, Verneri, Grove, Jakob, Holmans, Peter, Huang, Hailiang, Klei, Lambertus, Lee, Phil H, Medland, Sarah E, Neale, Benjamin, Robinson, Elise, Weiss, Lauren A, Zwaigenbaum, Lonnie, Yu, Timothy W, Wittemeyer, Kerstin, Willsey, a Jeremy, Wijsman, Ellen M, Werge, Thomas, Wassink, Thomas H, Waltes, Regina, Walsh, Christopher A, Wallace, Simon, Vorstman, Jacob a S, Vieland, Veronica J, Vicente, Astrid M, Vanengeland, Herman, Tsang, Kathryn, Thompson, Ann P, Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W, Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W, Schellenberg, Gerard D, Sandin, Sven, Sanders, Stephan J, Saemundsen, Evald, Rouleau, Guy A, Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S, Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A, Pejovic-Milovancevic, Milica, Pedersen, Marianne Giørtz, Pedersen, Carsten Bøcker, Paterson, Andrew D, Parr, Jeremy R, Pagnamenta, Alistair T, Oliveira, Guiomar, Nurnberger, John I, Nordentoft, Merete, Murtha, Michael T, Mouga, Susana, Mortensen, Preben Bo, Mors, Ole, Morrow, Eric M, Moreno-De-Luca, Daniel, Monaco, Anthony P, Minshew, Nancy, Merikangas, Alison, Mcmahon, William M, Mcgrew, Susan G, Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M, Mane, Shrikant M, Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K, Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H, Leboyer, Marion, Lecouteur, Ann S, Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M, Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M, Hougaard, David M, Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine Søholm, Haines, Jonathan L

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The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling by Franquinho, Filipa, Nogueira-Rodrigues, Joana, Duarte, Joana M, Esteves, Sofia S, Carter-Su, Christin, Monaco, Anthony P, Molnár, Zoltán, Velayos-Baeza, Antonio, Brites, Pedro, Sousa, Mónica M

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PCSK6 is associated with handedness in individuals with dyslexia by SCERRI, Thomas S, BRANDLER, William M, PARACCHINI, Silvia, MORRIS, Andrew P, RING, Susan M, RICHARDSON, Alex J, TALCOTT, Joel B, STEIN, John, MONACO, Anthony P

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