A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
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.
Published in Molecular psychiatry (01.07.2019)
Published in Molecular psychiatry (01.07.2019)
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Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
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
Published in PLoS genetics (01.09.2013)
Published in PLoS genetics (01.09.2013)
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A common variant associated with dyslexia reduces expression of the KIAA0319 gene
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
Published in PLoS genetics (01.03.2009)
Published in PLoS genetics (01.03.2009)
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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
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
Published in PloS one (28.11.2012)
Published in PloS one (28.11.2012)
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Identification of candidate genes for dyslexia susceptibility on chromosome 18
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
Published in PloS one (28.10.2010)
Published in PloS one (28.10.2010)
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Journal Article
Genetics of developmental dyslexia
Scerri, Thomas S., Schulte-Körne, Gerd
Published in European child & adolescent psychiatry (01.03.2010)
Published in European child & adolescent psychiatry (01.03.2010)
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Genome-wide analyses identify common variants associated with macular telangiectasia type 2
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
Published in Nature genetics (01.04.2017)
Published in Nature genetics (01.04.2017)
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Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation
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
Published in Neurology (19.05.2020)
Published in Neurology (19.05.2020)
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An α-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer
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
Published in The Journal of pathology (01.03.2013)
Published in The Journal of pathology (01.03.2013)
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Journal Article
Atypical development of Broca's area in a large family with inherited stuttering
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
Published in Brain (London, England : 1878) (29.04.2022)
Published in Brain (London, England : 1878) (29.04.2022)
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Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40
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
Published in Brain (London, England : 1878) (01.12.2023)
Published in Brain (London, England : 1878) (01.12.2023)
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Journal Article
PCSK6 is associated with handedness in individuals with dyslexia
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
Published in Human molecular genetics (01.02.2011)
Published in Human molecular genetics (01.02.2011)
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Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia
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
Published in Genetics in medicine (01.11.2019)
Published in Genetics in medicine (01.11.2019)
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Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
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
Published in Biological psychiatry (1969) (15.08.2010)
Published in Biological psychiatry (1969) (15.08.2010)
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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
Published in Developmental medicine and child neurology (01.04.2014)
Published in Developmental medicine and child neurology (01.04.2014)
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Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18
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.
Published in PloS one (15.12.2010)
Published in PloS one (15.12.2010)
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Journal Article
An [alpha]-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer
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
Published in The Journal of pathology (01.03.2013)
Published in The Journal of pathology (01.03.2013)
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Journal Article
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill: e1003751
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
Published in PLoS genetics (01.09.2013)
Published in PLoS genetics (01.09.2013)
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Journal Article
A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene: e1000436
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
Published in PLoS genetics (01.03.2009)
Published in PLoS genetics (01.03.2009)
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Journal Article