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

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

المؤلفون: HOOPER, E., SIMKIN, Z., ABRAMS, H., CAMACHO, E., CHARALAMBOUS, A. P., COLLIN, Fideline, CONSTANTINIDOU, F., DAWES, P., ELLIOTT, R., FALKINGHAM, S., FRISON, Éric, HANN, M., HELMER, Catherine, HIMMELSBACH, I., HUSSAIN, H., MARIE, S., MONTECELO, S., REEVES, D., REGAN, J., THODI, C., WOLSKI, L., LEROI, I.

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______9631::f1e5aa6bf83806007edd72cb9286573b
http://hdl.handle.net/20.500.12278/39043

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: Falcaro, M., Pickles, A., Newbury, D., Addis, L., Banfield, E., Fisher, S., Monaco, A., Simkin, Z., Conti-Ramsden, G., Consortium

المصدر: Genes, Brain and Behavior

مصطلحات موضوعية: Male, Genotype, Genetic Linkage, DNA Mutational Analysis, Short-term memory, Verb, Specific language impairment, Past tense, Behavioral Neuroscience, Chromosome 16, Genetic linkage, Chromosome 19, Genetics, medicine, Humans, Genetic Predisposition to Disease, Language Development Disorders, Genetic Testing, Child, Language, Memory Disorders, Language Tests, Learning Disabilities, Verbal Behavior, Family aggregation, Chromosome Mapping, medicine.disease, Memory, Short-Term, Phenotype, Neurology, Female, Psychology, Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 16

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c36d6fda09c082624891e3f77319810
https://doi.org/10.1111/j.1601-183x.2007.00364.x

المؤلفون: Simpson, Nuala H, Ceroni, Fabiola, Reader, Rose H, Covill, Laura E, Knight, Julian C, Nudel, R, Monaco, A P, Simonoff, E, Bolton, P F, Pickles, A, Slonims, V, Dworzynski, K, Everitt, A, Clark, A, Watson, J, Seckl, J, Cowie, H, Cohen, W, Nasir, Jamal, Bishop, D V M, Simkin, Z, Hennessy, Elizabeth R, Bolton, Patrick F, Conti-Ramsden, Gina, O'Hare, Anne, Baird, Gillian, Fisher, Simon E, Newbury, Dianne F

المصدر: 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, Bolton, P F, 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 2015, ' Genome-wide analysis identifies a role for common copy number variants in specific language impairment ', European journal of human genetics : EJHG, vol. 23, no. 10, pp. 1370-1377 . https://doi.org/10.1038/ejhg.2014.296

مصطلحات موضوعية: RZ, A100, QH426

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::82e6936c4f6efe1d1b8b76790816c347
https://strathprints.strath.ac.uk/55421/1/Simpson_etal_EJHG_2016_Genome_wide_analysis_identifies_a_role_for_common_copy_number_variants_in_specific.pdf

المؤلفون: 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., Nudel, R., Monaco, A. P., Francks, C., Baird, G., Slonims, V., Dworzynski, K., Bolton, P. F., Simonoff, E., O'Hare, A., Seckl, J., Cowie, H., Clark, A., Watson, J., Nasir, J., Cohen, W., Everitt, A., Hennessy, E. R., Shaw, D., Helms, P. J., Simkin, Z., Conti, G., Ramsden, D., Bishop, D. V M, Pickles, A.

مصطلحات موضوعية: RM

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::e21fcf510e07074fb271fd3fb7edea4d
https://strathprints.strath.ac.uk/53033/1/Pettigrew_etal_GBB_2015_Lack_of_replication_for_the_myosin_18B_association_with_mathematical.pdf

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, Nudel, R, Monaco, AP, Simonoff, E, Pickles, A, Everitt, A, Seckl, J, Cowie, H, Cohen, W, Nasir, J, Bishop, DVM, Simkin, Z

المصدر: Developmental Medicine and Child Neurology. 56(4)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1064::c3993d789321c9e5de7e1e90a70ff92c
http://ora.ox.ac.uk/objects/uuid:d25e55ca-771b-495f-9989-04f85be2b81f

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