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Hits 21 – 40 of 54

21	Comorbidities in preschool children at family risk of dyslexia.
	Gooch, D; Hulme, C; Nash, HM...
	In: J Child Psychol Psychiatry , 55 (3) 237 - 246. (2014) (2014)
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22	Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism
	El-Kordi, Ahmed; Winkler, Daniela; Hammerschmidt, Kurt...
	In: ISSN: 0166-4328 ; EISSN: 1872-7549 ; Behavioural Brain Research ; https://hal-pasteur.archives-ouvertes.fr/pasteur-01580131 ; Behavioural Brain Research, Elsevier, 2013, 251 (1), pp.41 - 49. ⟨10.1016/j.bbr.2012.11.016⟩ (2013)
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23	The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies.
	Steinberg, J; Webber, C
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013)
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24	Cerebral asymmetry and language development: cause, correlate, or consequence?
	Bishop, DV
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013)
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25	TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.
	Wiszniewski, W; Hunter, JV; Hanchard, NA...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013)
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26	New insight on the Xq28 association with systemic sclerosis.
	Carmona, FD; Cénit, MC; Diaz-Gallo, LM...
	In: Ann Rheum Dis , 72 (12) 2032 - 2038. (2013) (2013)
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27	A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci
	J. Martin; S. Assassi; L. Diaz-Gallo. - : Oxford University Press, 2013
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28	Individual common variants exert weak effects on the risk for autism spectrum disorders.
	Anney, Richard; Klei, Lambertus; Pinto, Dalila...
	In: Human molecular genetics, vol 21, iss 21 (2012)
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29	Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
	Anney, R; Klei, L; Pinto, D...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef ; ORA review team (2012)
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30	Child and parental literacy levels within families with a history of dyslexia.
	van der Leij, A; Plakas, A; Maassen, B...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Scopus (http://www.scopus.com/home.url) ; CrossRef ; ORA review team (2012)
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31	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
	Gorlova, Olga; Martin, Jose-Ezequiel; Rueda, Blanca...
	In: PLoS genetics, vol 7, iss 7 (2011)
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32	Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
	Newbury, DF; Paracchini, S; Scerri, TS...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011)
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33	Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.
	Villanueva, P; Newbury, DF; Jara, L...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011)
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34	CNTNAP2 variants affect early language development in the general population.
	Whitehouse, AJ; Bishop, DV; Fisher, SE...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef ; ORA review team (2011)
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35	A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.
	Addis, L; Friederici, AD; Kotz, SA...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2010)
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36	A specific pathway can be identified between genetic characteristics and behaviour profiles in Prader-Willi syndrome via cognitive, environmental and physiological mechanisms.
	Woodcock, KA; Oliver, C; Humphreys, GW
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009)
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37	Relations among speech, language, and reading disorders.
	Pennington, BF; Bishop, DV
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009)
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38	Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.
	Falcaro, M; Pickles, A; Newbury, DF...
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2008)
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39	AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review.
	Braissant, O.; Henry, H.
	In: Journal of Inherited Metabolic Disease, vol. 31, no. 2, pp. 230-239 (2008)
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40	The broader language phenotype of autism: a comparison with specific language impairment.
	Whitehouse, AJ; Barry, JG; Bishop, DV
	In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2007)
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