A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development von Eising, Else, Carrion-Castillo, Amaia, Vino, Arianna, Strand, Edythe A., Jakielski, Kathy J., Scerri, Thomas S., Hildebrand, Michael S., Webster, Richard, Ma, Alan, Mazoyer, Bernard, Francks, Clyde, Bahlo, Melanie, Scheffer, Ingrid E., Morgan, Angela T., Shriberg, Lawrence D., Fisher, Simon E.

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Common variants in left/right asymmetry genes and pathways are associated with relative hand skill von 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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A common variant associated with dyslexia reduces expression of the KIAA0319 gene von Dennis, Megan Y, Paracchini, Silvia, Scerri, Thomas S, Prokunina-Olsson, Ludmila, Knight, Julian C, Wade-Martins, Richard, Coggill, Penny, Beck, Stephan, Green, Eric D, Monaco, Anthony P

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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure von Scerri, Thomas S, Darki, Fahimeh, Newbury, Dianne F, Whitehouse, Andrew J O, Peyrard-Janvid, Myriam, Matsson, Hans, Ang, Qi W, Pennell, Craig E, Ring, Susan, Stein, John, Morris, Andrew P, Monaco, Anthony P, Kere, Juha, Talcott, Joel B, Klingberg, Torkel, Paracchini, Silvia

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Identification of candidate genes for dyslexia susceptibility on chromosome 18 von Scerri, Thomas S, Paracchini, Silvia, Morris, Andrew, MacPhie, I Laurence, Talcott, Joel, Stein, John, Smith, Shelley D, Pennington, Bruce F, Olson, Richard K, DeFries, John C, Monaco, Anthony P, Richardson, Alex J

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Genetics of developmental dyslexia von Scerri, Thomas S., Schulte-Körne, Gerd

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Genome-wide analyses identify common variants associated with macular telangiectasia type 2 von Scerri, Thomas S, Quaglieri, Anna, Cai, Carolyn, Zernant, Jana, Matsunami, Nori, Baird, Lisa, Scheppke, Lea, Bonelli, Roberto, Yannuzzi, Lawrence A, Friedlander, Martin, Egan, Catherine A, Fruttiger, Marcus, Leppert, Mark, Allikmets, Rando, Bahlo, Melanie

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Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation von Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Van Reyk, Olivia, Coleman, Matthew, Braden, Ruth O., Turner, Samantha, Rigbye, Kristin A., Boys, Amber, Barton, Sarah, Webster, Richard, Fahey, Michael, Saunders, Kerryn, Parry-Fielder, Bronwyn, Paxton, Georgia, Hayman, Michael, Coman, David, Goel, Himanshu, Baxter, Anne, Ma, Alan, Davis, Noni, Reilly, Sheena, Delatycki, Martin, Liégeois, Frederique J., Connelly, Alan, Gecz, Jozef, Fisher, Simon E., Amor, David J., Scheffer, Ingrid E., Bahlo, Melanie, Morgan, Angela T.

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An α-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer von Majewski, Ian J, Kluijt, Irma, Cats, Annemieke, Scerri, Thomas S, de Jong, Daphne, Kluin, Roelof JC, Hansford, Samantha, Hogervorst, Frans BL, Bosma, Astrid J, Hofland, Ingrid, Winter, Marcel, Huntsman, David, Jonkers, Jos, Bahlo, Melanie, Bernards, René

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Atypical development of Broca's area in a large family with inherited stuttering von Thompson-Lake, Daisy G Y, Scerri, Thomas S, Block, Susan, Turner, Samantha J, Reilly, Sheena, Kefalianos, Elaina, Bonthrone, Alexandra F, Helbig, Ingo, Bahlo, Melanie, Scheffer, Ingrid E, Hildebrand, Michael S, Liégeois, Frédérique J, Morgan, Angela T

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Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40 von Morgan, Angela T, Scerri, Thomas S, Vogel, Adam P, Reid, Christopher A, Quach, Mara, Jackson, Victoria E, McKenzie, Chaseley, Burrows, Emma L, Bennett, Mark F, Turner, Samantha J, Reilly, Sheena, Horton, Sarah E, Block, Susan, Kefalianos, Elaina, Frigerio-Domingues, Carlos, Sainz, Eduardo, Rigbye, Kristin A, Featherby, Travis J, Richards, Kay L, Kueh, Andrew, Herold, Marco J, Corbett, Mark A, Gecz, Jozef, Helbig, Ingo, Thompson-Lake, Daisy G Y, Liégeois, Frédérique J, Morell, Robert J, Hung, Andrew, Drayna, Dennis, Scheffer, Ingrid E, Wright, David K, Bahlo, Melanie, Hildebrand, Michael S

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PCSK6 is associated with handedness in individuals with dyslexia von 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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Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia von Khan, Kamal, Zech, Michael, Morgan, Angela T., Amor, David J., Skorvanek, Matej, Khan, Tahir N., Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Coleman, Matthew, Rigbye, Kristin A., Scheffer, Ingrid E., Bahlo, Melanie, Wagner, Matias, Lam, Daniel D., Berutti, Riccardo, Havránková, Petra, Fečíková, Anna, Strom, Tim M., Han, Vladimir, Dosekova, Petra, Gdovinova, Zuzana, Laccone, Franco, Jameel, Muhammad, Mooney, Marie R., Baig, Shahid M., Jech, Robert, Davis, Erica E., Katsanis, Nicholas, Winkelmann, Juliane

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Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia von 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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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia von Simpson, Nuala H, Addis, Laura, Brandler, William M, Slonims, Vicky, Clark, Ann, Watson, Jocelynne, Scerri, Thomas S, Hennessy, Elizabeth R, Bolton, Patrick F, Conti‐Ramsden, Gina, Fairfax, Benjamin P, Knight, Julian C, Stein, John, Talcott, Joel B, O'Hare, Anne, Baird, Gillian, Paracchini, Silvia, Fisher, Simon E, Newbury, Dianne F, Consortium, SLI

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Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18 von Scerri, Thomas S., Paracchini, Silvia, Morris, Andrew, MacPhie, I. Laurence, Talcott, Joel, Stein, John, Smith, Shelley D., Pennington, Bruce F., Olson, Richard K., DeFries, John C., Monaco, Anthony P., Richardson, Alex J.

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Genetics of developmental dyslexia: Unraveling the molecular genetic basis of child and adolescent psychiatric disorders von SCERRI, Thomas S, SCHULTE-KÖRNE, Gerd

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An [alpha]-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer von Majewski, Ian J, Kluijt, Irma, Cats, Annemieke, Scerri, Thomas S, Jong, Daphne, Kluin, Roelof JC, Hansford, Samantha, Hogervorst, Frans BL, Bosma, Astrid J, Hofland, Ingrid, Winter, Marcel, Huntsman, David, Jonkers, Jos, Bahlo, Melanie, Bernards, René

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Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill: e1003751 von Brandler, William M, Morris, Andrew P, Evans, David M, Scerri, Thomas S, Kemp, John P, Timpson, Nicholas J, Pourcain, Beate St, 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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A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene: e1000436 von Dennis, Megan Y, Paracchini, Silvia, Scerri, Thomas S, Prokunina-Olsson, Ludmila, Knight, Julian C, Wade-Martins, Richard, Coggill, Penny, Beck, Stephan, Green, Eric D, Monaco, Anthony P

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