PCSK6 is associated with handedness in individuals with dyslexia

Por 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.
Publicado em 2011

A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene

Por 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.
Publicado em 2009

Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18

Por 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.
Publicado em 2010

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18

Por 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.
Publicado em 2010

Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR

Por Leventer, Richard J., Scerri, Thomas, Marsh, Ashley P.L., Pope, Kate, Gillies, Greta, Maixner, Wirginia, MacGregor, Duncan, Harvey, A. Simon, Delatycki, Martin B., Amor, David J., Crino, Peter, Bahlo, Melanie, Lockhart, Paul J.
Publicado no Neurology (2015)

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure

Por 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
Publicado em 2012

Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill

Por 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
Publicado em 2013

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

Por 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
Publicado no Dev Med Child Neurol (2014)

Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5

Por Scerri, Thomas, Riseley, Jessica R, Gillies, Greta, Pope, Kate, Burgess, Rosemary, Mandelstam, Simone A, Dibbens, Leanne, Chow, Chung W, Maixner, Wirginia, Harvey, Anthony Simon, Jackson, Graeme D, Amor, David J, Delatycki, Martin B, Crino, Peter B, Berkovic, Samuel F, Scheffer, Ingrid E, Bahlo, Melanie, Lockhart, Paul J, Leventer, Richard J
Publicado no Ann Clin Transl Neurol (2015)

Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency

Por Fliegauf, Manfred, L. Bryant, Vanessa, Frede, Natalie, Slade, Charlotte, Woon, See-Tarn, Lehnert, Klaus, Winzer, Sandra, Bulashevska, Alla, Scerri, Thomas, Leung, Euphemia, Jordan, Anthony, Keller, Baerbel, de Vries, Esther, Cao, Hongzhi, Yang, Fang, Schäffer, Alejandro A., Warnatz, Klaus, Browett, Peter, Douglass, Jo, Ameratunga, Rohan V., van der Meer, Jos W.M., Grimbacher, Bodo
Publicado no Am J Hum Genet (2015)

Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

Por de Vos, Ivo J H M, Tao, Evelyn Yaqiong, Ong, Sheena Li Ming, Goggi, Julian L, Scerri, Thomas, Wilson, Gabrielle R, Low, Chernis Guai Mun, Wong, Arnette Shi Wei, Grussu, Dominic, Stegmann, Alexander P A, van Geel, Michel, Janssen, Renske, Amor, David J, Bahlo, Melanie, Dunn, Norris R, Carney, Thomas J, Lockhart, Paul J, Coull, Barry J, van Steensel, Maurice A M
Publicado no Hum Mol Genet (2018)

Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

Por 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.
Publicado em 2010