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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 Hits 1 – 20 of 21 1 The trans-ancestral genomic architecture of glycemic traits. Chen, J.; Spracklen, C.N.; Marenne, G.... In: Nature genetics, vol. 53, no. 6, pp. 840-860 (2021) BASE Show details 2 Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay. Ansar, M.; Riazuddin, S.; Sarwar, M.T.... In: Genetics in medicine, vol. 20, no. 7, pp. 778-784 (2018) BASE Show details 3 Unexpected Island Effects at an Extreme: Reduced Y Chromosome and Mitochondrial DNA Diversity in Nias van Oven, Mannis; Hammerle, Johannes M.; van Schoor, Marja... In: Molecular Biology and Evolution (2015) BASE Show details 4 Unexpected Island Effects at an Extreme: Reduced Y Chromosome and Mitochondrial DNA Diversity in Nias van Oven, Mannis; Hammerle, Johannes M.; van Schoor, Marja... In: Molecular Biology and Evolution (2015) BASE Show details 5 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) BASE Show details 6 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) BASE Show details 7 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) BASE Show details 8 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) BASE Show details 9 Fuzzy association rules for biological data analysis: A case study on yeast López Domingo, Francisco Javier; Blanco Morón, Armando; García Alcalde, Fernando. - : Biomed Central, 2008 BASE Show details 10 Molecular windows into speech and language disorders. 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 (2007) BASE Show details 11 Y-chromosomal diversity in the population of Guinea-Bissau: a multiethnic perspective Rosa, Alexandra; Ornelas, Carolina; Jobling, Mark A.. - : BMC, 2007 BASE Show details 12 Generalist genes and cognitive neuroscience Butcher, LM; Kennedy, JK; Plomin, R In: Curr.Opin.Neurobiol. , 16 (2) pp. 145-151. (2006) (2006) BASE Show details 13 Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression. Parr, JR; Lamb, JA; Bailey, AJ... 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 (2006) BASE Show details 14 Genetic influences on language impairment and phonological short-term memory. Monaco, AP; Bishop, DV; 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 (2005) BASE Show details 15 A genome-wide scan for childhood obesity-associated traits in French families shows significant linkage on chromosome 6q22.31-q23.2. Meyre, David; Lecoeur, Cécile; Delplanque, Jérôme... In: ISSN: 0012-1797 ; EISSN: 0012-1797 ; Diabetes ; https://hal.archives-ouvertes.fr/hal-00174547 ; Diabetes, American Diabetes Association, 2004, 53 (3), pp.803-11 (2004) BASE Show details 16 Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment. In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; ORA review team (2004) BASE Show details 17 Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits. Smith, M; Woodroffe, A; Smith, R... In: Cytogenetic and genome research, vol 98, iss 4 (2002) BASE Show details 18 A genomewide scan identifies two novel loci involved in specific language impairment. 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) ; ORA review team (2002) BASE Show details 19 Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Fisher, SE; Francks, C; Marlow, AJ... 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 (2002) BASE Show details 20 The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. Lai, CS; Fisher, SE; Hurst, JA... 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 (2000) BASE Show details Page: 1 2

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