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Number of items: 28.

2019

Talcott, Joel B, Patel, Tulpesh, Griffiths, Gareth, Kelly, Deirdre and Beath, Sue V. (2019). Long-term Effects of Cholestatic Liver Disease in Childhood on Neuropsychological Outcomes and Neurochemistry. Journal of Pediatric Gastroenterology and Nutrition, 69 (2), pp. 145-151.

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 and Schulte-körne, Gerd (2019). Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational psychiatry, 9 (1), p. 77.

Murphy, Kelly, Talcott, Joel B and Jogia, Jigar R (2019). On the neural basis of word reading:A meta-analysis of fMRI evidence using activation likelihood estimation. Journal of Neurolinguistics, 49 , pp. 71-83.

2017

Phan, Thanh Vân, Smeets, Dirk, Talcott, Joel B. and Vandermosten, Maaike (2017). Processing of structural neuroimaging data in young children:bridging the gap between current practice and state-of-the-art methods. Developmental Cognitive Neuroscience, Early ,

Scerri, T S, Macpherson, E, Martinelli, A, Wa, W C, Monaco, A P, Stein, J, Zheng, M, Suk-Han Ho, C, McBride, C, Snowling, M, Hulme, C, Hayiou-Thomas, M E, Waye, M M Y, Talcott, Joel B and Paracchini, S (2017). The DCDC2 deletion is not a risk factor for dyslexia. Translational psychiatry, 7 ,

Eckert, Mark A., Vaden Jr., Kenneth I., Maxwell, Amanda B., Cute, Stephanie L., Gebregziabher, Mulugeta, Berninger, Virginia W., Talcott, J. and Wandell, B. (2017). Common brain structure findings across children with varied reading disability profiles. Scientific Reports, 7 ,

Witton, Caroline, Talcott, Joel B. and Henning, G. Bruce (2017). Psychophysical measurements in children:challenges, pitfalls, and considerations. PeerJ, 2017 (5),

2016

Pettigrew, Kerry A., Frinton, Emily, Nudel, Ron, Chan, May T.M., Thompson, Paul, Hayiou-Thomas, Marianna E., Talcott, Joel B., Stein, John, Monaco, Anthony P., Hulme, Charles, Snowling, Margaret J., Newbury, Dianne F. and Paracchini, Silvia (2016). Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes. Journal of Neurodevelopmental Disorders, 8 ,

Shore, Robert, Covill, Laura, Pettigrew, Kerry A., Brandler, William M., Diaz, Rebeca, Xu, Yiwang, Tello, Javier A., Talcott, Joel B., Newbury, Dianne F., Stein, John, Monaco, Anthony P. and Paracchini, Silvia (2016). The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts. Human Molecular Genetics, 25 (9), pp. 1771-1779.

2015

Cunningham, Anna J., Witton, Caroline, Talcott, Joel B., Burgess, Adrian P. and Shapiro, Laura R. (2015). Deconstructing phonological tasks:the contribution of stimulus and response type to the prediction of early decoding skills. Cognition, 143 , pp. 178-186.

Ivanova, Masha Y., Achenbach, Thomas M., Rescorla, Leslie A., Turner, Lori V., Ahmeti-Pronaj, Adelina, Au, Alma, Avila Maese, Carmen, Bellina, Monica, Caldas, J. Carlos, Chen, Yi-Chuen, Csemy, Ladislav, da Rocha, Marina M., Decoster, Jeroen, Dobrean, Anca, Ezpeleta, Lourdes, Fontaine, Johnny R.J., Funabiki, Yasuko, Guðmundsson, Halldór S., Harder, Valerie S., Leiner de la Cabada, Marie, Leung, Patrick, Liu, Jianghong, Mahr, Safia, Malykh, Sergey, Srdanovic Maras, Jelena, Markovic, Jasminka, Ndetei, David M., Oh, Kyung Ja, Petot, Jean-Michel, Riad, Geylan, Sakarya, Direnc, Samaniego, Virginia C., Sebre, Sandra, Shahini, Mimoza, Silvares, Edwiges, Simulioniene, Roma, Sokoli, Elvisa, Talcott, Joel B., Vázquez, Natalia and Zasępa, Ewa (2015). Syndromes of self-reported psychopathology for ages 18-59 in 29 societies. Journal of Psychopathology and Behavioral Assessment, 37 (2), pp. 171-183.

Ivanova, Masha Y., Achenbach, Thomas M., Rescorla, Leslie A., Turner, Lori V., Árnadóttir, Hervör Alma, Au, Alma, Caldas, J. Carlos, Chaalal, Nebia, Chen, Yi Chuen, da Rocha, Marina M., Decoster, Jeroen, Fontaine, Johnny R.J., Funabiki, Yasuko, Guðmundsson, Halldór S., Kim, Young Ah, Leung, Patrick, Liu, Jianghong, Malykh, Sergey, Marković, Jasminka, Oh, Kyung Ja, Petot, Jean-Michel, Samaniego, Virginia C., Ferreira de Mattos Silvares, Edwiges, Šimulionienė, Roma, Šobot, Valentina, Sokoli, Elvisa, Sun, Guiju, Talcott, Joel B., Vázquez, Natalia and Zasępa, Ewa (2015). Syndromes of collateral-reported psychopathology for ages 18-59 in 18 societies. International Journal of Clinical and Health Psychology, 15 (1), pp. 18-28.

2014

Cassim, Rizan, Talcott, Joel and Moores, Elisabeth (2014). Adults with dyslexia demonstrate large effects of crowding and detrimental effects of distractors in a visual tilt discrimination task. PLoS ONE, 9 (9),

Gialluisi, A., Newbury, D.F., Wilcutt, E.G., Olson, R.K., DeFries, J.C., Brandler, W.M., Pennington, B.F., Smith, S.D., Scerri, T.S., Simpson, N.H., SLI Consortium, Luciano, M., Evans, D.M., Bates, T.C., Stein, J.F., Talcott, J.B., Monaco, A.P., Paracchini, S., Francks, C. and Fisher, S.E. (2014). Genome-wide screening for DNA variants associated with reading and language traits. Genes, Brain and Behavior, 13 (7), 686–701.

Loras, Håvard, Sigmundsson, Hermundur, Stensdotter, Ann-Katrin and Talcott, Joel B. (2014). Postural control is not systematically related to reading skills:implications for the assessment of balance as a risk factor for developmental dyslexia. PLoS ONE, 9 (6),

Becker, Jessica, Czamara, Darina, Scerri, Tom S., Ramus, Franck, Csépe, Valéria, Talcott, Joel B., Stein, John, Morris, Andrew, Ludwig, Kerstin U., Hoffmann, Per, Honbolygó, Ferenc, Tóth, Dénes, Fauchereau, Fabien, Bogliotti, Caroline, Iannuzzi, Stéphanie, Chaix, Yves, Valdois, Sylviane, Billard, Catherine, George, Florence, Soares-Boucaud, Isabelle, Gérard, Christophe-Loïc, van der Mark, Sanne, Schulz, Enrico, Vaessen, Anniek, Maurer, Urs, Lohvansuu, Kaisa, Lyytinen, Heikki, Zucchelli, Marco, Brandeis, Daniel, Blomert, Leo, Leppänen, Paavo H.T., Bruder, Jennifer, Monaco, Anthony P., Müller-Myhsok, Bertram, Kere, Juha, Landerl, Karin, Nöthen, Markus M., Schulte-Körne, Gerd, Paracchini, Silvia, Peyrard-Janvid, Myriam and Schumacher, Johannes (2014). Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. European Journal of Human Genetics, 22 (5), pp. 675-680.

Patel, Tulpesh, Blyth, Jacqueline C., Griffiths, Gareth, Kelly, Deirdre and Talcott, Joel B. (2014). Moderate relationships between NAA and cognitive ability in healthy adults:implications for cognitive spectroscopy. Frontiers in Human Neuroscience, 8 ,

2013

Brandler, William M., Morris, Andrew P., Evans, David M., Scerri, Thomas S., Kemp, John P., Timpson, Nicholas J., St Pourcain, Beate, Smith, George D., Ring, Susan M., Stein, John, Monaco, Anthony P., Talcott, Joel B., Fisher, Simon E., Webber, Caleb and Paracchini, Silvia (2013). Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. PLoS Genetics, 9 (9),

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 F., Talcott, Joel B., O'Hare, Anne, Baird, Gillian, Paracchini, Silvia, Fisher, Simon E., Newbury, Dianne F. and SLI Consortium (2013). Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine and Child Neurology, 56 (4), pp. 346-353.

2012

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, Klingberg, Torkel and Paracchini, Silvia (2012). The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. PLoS ONE, 7 (11),

Birkett, Emma and Talcott, Joel (2012). Interval timing in children:effects of auditory and visual pacing stimuli and relationships with reading and attention variables. PLoS ONE, 7 (8),

Cunningham, Anna, Shapiro, Laura, Witton, Caroline, Talcott, Joel, Rochelle, Kim and Burgess, Adrian (2012). Speech and non-speech skills in the prediction of letter-knowledge:the influence of task. IN: 2nd meeting of the EARLI SIG Neuroscience and Education. Institute of Education, 2012-05-24 - 2012-05-26. (Unpublished)

2011

Moores, Elisabeth, Cassim, Rizan and Talcott, Joel B. (2011). Adults with dyslexia exhibit large effects of crowding, increased dependence on cues, and detrimental effects of distractors in visual search tasks. Neuropsychologia, 49 (14), pp. 3881-3890.

Scerri, Thomas S., Brandler, William M., Paracchini, Silvia, Morris, Andrew P., Ring, Susan M., Richardson, Alex J., Talcott, Joel B., Stein, John F. and Monaco, Anthony P. (2011). PCSK6 is associated with handedness in individuals with dyslexia. Human Molecular Genetics, 20 (3), pp. 608-614.

Newbury, D.F., Paracchini, S., Scerri, T.S., Winchester, L., Addis, L., Richardson, A.J., Walter, J., Stein, J.F., Talcott, J.B. and Monaco, A.P. (2011). Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behavior Genetics, 41 (1), pp. 90-104.

2010

Scerri, Thomas S., Paracchini, Silvia, Morris, Andrew, MacPhie, I. Laurence, Talcott, Joel B., Stein, John F., Smith, Shelley D., Pennington, Bruce F., Olson, Richard K., DeFries, John C., Monaco, Anthony P. and Richardson, Alex J. (2010). Identification of candidate genes for dyslexia susceptibility on chromosome 18. PLoS ONE, 5 (10),

2006

Rochelle, Kim S. H. and Talcott, Joel B. (2006). Impaired balance in developmental dyslexia? A meta-analysis of the contending evidence. Journal of Child Psychology and Psychiatry, 47 (11), pp. 1159-1166.

2002

Rae, Caroline, Harasty, Jenny A., Dzendrowskyj, Theresa E., Talcott, Joel B., Simpson, Judy M., Blamire, Andrew M., Dixon, Ruth M., Lee, Martin A., Thompson, Campbell H., Styles, Peter, Richardson, Alex J. and Stein, John F. (2002). Cerebellar morphology in developmental dyslexia. Neuropsychologia, 40 (8), pp. 1285-1292.

This list was generated on Tue Aug 20 02:58:42 2019 BST.