المؤلفون: Durkin, K., Conti-Ramsden, G., Walker, A. J.

المصدر: Journal of Computer Assisted Learning. Feb 2011 27(1):49-57.

Peer Reviewed: Y

Page Count: 9

Descriptors: Language Impairments, Adolescents, Reading Ability, Educational Technology, Literacy, Written Language, Telecommunications, Cognitive Ability, Language Skills, Correlation

المؤلفون: Botting, N., Simkin, Z, Conti-Ramsden, G.

المصدر: Reading and Writing: An Interdisciplinary Journal. Feb 2006 19(1):77-98.

Peer Reviewed: Y

Page Count: 22

Descriptors: Reading Skills, Children, Language Impairments, Emergent Literacy, Reading Tests, Age, Intelligence Quotient, Early Reading, Phonology, Syntax, Student Evaluation, Dyslexia

المؤلفون: Riches, N. G., Faragher, B., Conti-Ramsden, G.

المصدر: International Journal of Language and Communication Disorders. Mar-Apr 2006 41(2):117-135.

Peer Reviewed: Y

Page Count: 19

Descriptors: Verbs, Sentences, Nouns, Language Impairments, Children, Schemata (Cognition), Language Usage, Linguistic Input, Hypothesis Testing

URL الوصول: http://taylorandfrancis.metapress.com/link.asp?target=contribution&id=X128728074R4Q432

المؤلفون: Botting, N., Simkin, Z., Conti-Ramsden, G.

المصدر: Reading and Writing: An Interdisciplinary Journal. 02 2006 19(1):77-98

المؤلفون: Ceroni, F., Simpson, N.H., Francks, C., Baird, G., Conti-Ramsden, G., Clark, A., Bolton, P.F., Hennessy, E.R., Donnelly, P, Bentley, D.R., Martin, H., Parr, J., Pagnamenta, A.T., Maestrini, E., Bacchelli, E., Fisher, S.E., Newbury, D.F., Imgsac, ., Consortium, S.L.I., Consortium, W.G.S.

المصدر: European Journal of Human Genetics, 22, 10, pp. 1165-1171
European Journal of Human Genetics, 22, 1165-1171

مصطلحات موضوعية: Neuroinformatics

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5dcbf4b861adf2766c945278cbd6a197
https://doi.org/10.1038/ejhg.2014.4

المؤلفون: Simpson N. H., Ceroni F., Reader R. H., Covill L. E., Knight J. C., Hennessy E. R., Bolton P. F., Conti-Ramsden G., O'Hare A., Baird G., Fisher S. E., Newbury D. F., Nudel R., Monaco A. P., Simonoff E., Pickles A., Slonims V., Dworzynski K., Everitt A., Clark A., Watson J., Seckl J., Cowie H., Cohen W., Nasir J., Bishop D. V. M., Simkin Z.

المساهمون: Simpson N.H., Ceroni F., Reader R.H., Covill L.E., Knight J.C., Nudel R., Monaco A.P., Simonoff E., Pickles A., Slonims V., Dworzynski K., Everitt A., Clark A., Watson J., Seckl J., Cowie H., Cohen W., Nasir J., Bishop D.V.M., Simkin Z, Hennessy E.R., Bolton P.F., Conti-Ramsden G., O'Hare A., Baird G., Fisher S.E., Newbury D.F.

المصدر: European Journal of Human Genetics

مصطلحات موضوعية: Male, Language Disorders, Genome, DNA Copy Number Variations, Specific Language Impairment, Polymorphism, Single Nucleotide, Article, Copy Number Variations, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Aged, Genome-Wide Association Study, Language

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8d60e84bcb5b946a4c3d402f5d2fc50d
https://pubmed.ncbi.nlm.nih.gov/25585696

المؤلفون: Simpson, N, Addis, L, Brandler, WM, Slonims, V, Clark, A, Watson, J, Scerri, T, Hennessy, E, Bolton, P, Conti-Ramsden, G, Fairfax, B, Knight, J, Stein, J, Talcott, J, O'Hare, A, Baird, G, Paracchini, S, Fisher, SE, Newbury, D, Nudel, R, Monaco, A, Simonoff, E, Pickles, A, Everitt, A, Seckl, J

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1064::6e70613db3fe7874e25249d2dc5649e2
https://ora.ox.ac.uk/objects/uuid:d25e55ca-771b-495f-9989-04f85be2b81f

المؤلفون: Nudel, R., Simpson, N., Baird, G., O’Hare, A., Conti-Ramsden, G., Bolton, P., Hennessy, E., The SLli consortium, Ring, S., Smith, G., Francks, C., Paracchini, S., Monaco, A., Fisher, S., Newbury, D.

المساهمون: The Royal Society, University of St Andrews. School of Medicine, University of St Andrews. Biomedical Sciences Research Complex

المصدر: Genes, Brain and Behavior
Genes, Brain, and Behavior

مصطلحات موضوعية: Adult, Male, Genotype, Apraxias, Quantitative Trait Loci, QH426 Genetics, Polymorphism, Single Nucleotide, Genomic Imprinting, Neurodevelopmental disorder, RZ, Chromosomes, Human, Guanine Nucleotide Exchange Factors, Humans, GWAS, Child, QH426, Adaptor Proteins, Signal Transducing, Tumor Suppressor Proteins, RNA-Binding Proteins, Imprinting, Original Articles, ALSPAC, neurodevelopmental disorder, specific language impairment, Specific language impairment, RC0321, Female, imprinting, Apoptosis Regulatory Proteins, Receptors, Prostaglandin E, EP4 Subtype, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::336807296491e2f20459442ce6500f2f
https://ora.ox.ac.uk/objects/uuid:3c7de768-93bf-40f7-bff0-13bb7d05adf1

المؤلفون: Simpson, NH, Ceroni, F, Reader, RH, Covill, LE, Knight, JC, Hennessy, ER, Bolton, PF, Conti-Ramsden, G, O'Hare, A, Baird, G, Fisher, SE, Newbury, DF

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::22e358a90cad9df847226341beba90ca
https://ora.ox.ac.uk/objects/uuid:6abd09e5-d5ba-4000-b317-a6ac2dacf2d7

المؤلفون: Simpson, NH, Addis, L, Brandler, WM, Slonims, V, Clark, A, Watson, J, Scerri, TS, Hennessy, ER, Bolton, PF, Conti-Ramsden, G, Fairfax, BP, Knight, JC, Stein, J, Talcott, JB, O'Hare, A, Baird, G, Paracchini, S, Fisher, SE, Newbury, DF

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e86b41de9404a37a0eb15da12924ead2
https://ora.ox.ac.uk/objects/uuid:35f3b9a1-9f64-4867-a8f3-46271d28c7ac