Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects
Newbury, D. F., Paracchini, S., Scerri, T. S., Winchester, L., Addis, L., Richardson, Alex J., Walter, J., Stein, J. F., Talcott, J. B., Monaco, A. P.
Published in Behavior genetics (01.01.2011)
Published in Behavior genetics (01.01.2011)
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Journal Article
FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment
Newbury, D.F., Bonora, E., Lamb, J.A., Fisher, S.E., Lai, C.S.L., Baird, G., Jannoun, L., Slonims, V., Stott, C.M., Merricks, M.J., Bolton, P.F., Bailey, A.J., Monaco, A.P.
Published in American journal of human genetics (01.05.2002)
Published in American journal of human genetics (01.05.2002)
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Journal Article
Genetic and phenotypic effects of phonological short‐term memory and grammatical morphology in specific language impairment
Falcaro, M., Pickles, A., Newbury, D. F., Addis, L., Banfield, E., Fisher, S. E., Monaco, A. P., Simkin, Z., Conti‐Ramsden, G.
Published in Genes, brain and behavior (01.06.2008)
Published in Genes, brain and behavior (01.06.2008)
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Journal Article
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
Devanna, P, Chen, X S, Ho, J, Gajewski, D, Smith, S D, Gialluisi, A, Francks, C, Fisher, S E, Newbury, D F, Vernes, S C
Published in Molecular psychiatry (01.05.2018)
Published in Molecular psychiatry (01.05.2018)
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Journal Article
Genome‐wide screening for DNA variants associated with reading and language traits
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., Luciano, M., Evans, D. M., Bates, T. C., Stein, J. F., Talcott, J. B., Monaco, A. P., Paracchini, S., Francks, C., Fisher, S. E.
Published in Genes, brain and behavior (01.09.2014)
Published in Genes, brain and behavior (01.09.2014)
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Journal Article
Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment
Nudel, R., Simpson, N. H., Baird, G., O'Hare, A., Conti‐Ramsden, G., Bolton, P. F., Hennessy, E. R., Ring, S. M., Davey Smith, G., Francks, C., Paracchini, S., Monaco, A. P., Fisher, S. E., Newbury, D. F.
Published in Genes, brain and behavior (01.04.2014)
Published in Genes, brain and behavior (01.04.2014)
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Journal Article
Challenges for implementation in diverse settings: reflections on two randomised controlled trials of educational interventions in South American communities
Newbury, DF, Mesa, C, Puglisi, M, Nash, M, Nag, S, Hulme, C, Snowling, MJ
Published in Research papers in education (02.11.2023)
Published in Research papers in education (02.11.2023)
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Journal Article
Lack of replication for the myosin‐18B association with mathematical ability in independent cohorts
Pettigrew, K. A., Fajutrao Valles, S. F., Moll, K., Northstone, K., Ring, S., Pennell, C., Wang, C., Leavett, R., Hayiou‐Thomas, M. E., Thompson, P., Simpson, N. H., Fisher, S. E., Whitehouse, A. J. O., Snowling, M. J., Newbury, D. F., Paracchini, S.
Published in Genes, brain and behavior (01.04.2015)
Published in Genes, brain and behavior (01.04.2015)
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Journal Article
A genomewide scan identifies two novel loci involved in specific language impairment
Published in American journal of human genetics
(01.02.2002)
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Journal Article
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31‐q14.3
Addis, L., Friederici, A. D., Kotz, S. A., Sabisch, B., Barry, J., Richter, N., Ludwig, A. A., Rübsamen, R., Albert, F. W., Pääbo, S., Newbury, D. F., Monaco, A. P.
Published in Genes, brain and behavior (01.08.2010)
Published in Genes, brain and behavior (01.08.2010)
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Journal Article
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
Richardson, Alex J, Fisher, Simon E, Pennington, Bruce F, Stein, John F, Cardon, Lon R, Marlow, Angela J, Gayán, Javier, Francks, Clyde, Ishikawa-Brush, Yumiko, MacPhie, I. Laurence, Talcott, Joel B, Newbury, Dianne F, DeFries, John C, Monaco, Anthony P, Smith, Shelley D, Olson, Richard K
Published in Nature genetics (01.01.2002)
Published in Nature genetics (01.01.2002)
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Journal Article
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications
Wincent, J., Bruno, D.L., van Bon, B.W.M., Bremer, A., Stewart, H., Bongers, E.M.H.F., Ockeloen, C.W., Willemsen, M.H., Keays, D.A.D., Baird, G., Newbury, D.F., Kleefstra, T., Marcelis, C., Kini, U., Stark, Z., Savarirayan, R., Sheffield, L.J., Zuffardi, O., Slater, H.R., de Vries, B.B., Knight, S.J.L., Anderlid, B.-M., Schoumans, J.
Published in Molecular syndromology (01.01.2010)
Published in Molecular syndromology (01.01.2010)
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Journal Article
Mutation-specific pathophysiological mechanisms in a new SATB1-associated neurodevelopmental disorder
den Hoed, J., de Boer, E., Voisin, N., Guex, N., Blok, L. Snijders, Chrast, J., Manwaring, L., Willing, M., Waheeb, A., Osmond, M., Mcwalter, K., Vitobello, A., Demurger, F., Lavillaureix, A., Odent, S., Mazel, B., Faivre, L., Thiffault, I., Schwager, C., Amudhavalli, S. M., Rosenfeld, J. A., Radtke, K., Preiksaitiene, E., Ranza, E., Depienne, C., Kuechler, A., Mohammed, S., Abedi, Y. Hamzavi, Bonagura, V. R., Zuccarelli, B., Horist, B., Krishnamurthy, V., Kattentidt-Mouravieva, A. A., Granger, L., Petersen, A., Jones, K. L., Sinnema, M., Stegmann, A. P. A., Newbury-Ecob, R., Kini, U., Newbury, D. F., Gilissen, C., Brunner, H., Kleefstra, T., Reymond, A., Vissers, L. E. L. M., Fisher, S. E.
Published in European journal of human genetics : EJHG (2020)
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Published in European journal of human genetics : EJHG (2020)
Journal Article
Genetic influences on language impairment and phonological short-term memory
Newbury, Dianne F., Bishop, Dorothy V.M., Monaco, Anthony P.
Published in Trends in cognitive sciences (01.11.2005)
Published in Trends in cognitive sciences (01.11.2005)
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Journal Article
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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Journal Article
Highly Significant Linkage to the SLI1 Locus in an Expanded Sample of Individuals Affected by Specific Language Impairment
Published in American journal of human genetics
(01.06.2004)
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Journal Article
A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder
Fisher, Simon E., Francks, Clyde, McCracken, James T., McGough, James J., Marlow, Angela J., MacPhie, I. Laurence, Newbury, Dianne F., Crawford, Lori R., Palmer, Christina G.S., Woodward, J. Arthur, Del’Homme, Melissa, Cantwell, Dennis P., Nelson, Stanley F., Monaco, Anthony P., Smalley, Susan L.
Published in American journal of human genetics (01.05.2002)
Published in American journal of human genetics (01.05.2002)
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