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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 Hits 1 – 16 of 16 1 Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Bigdeli, Tim B; Genovese, Giulio; Georgakopoulos, Penelope... In: Molecular psychiatry, vol 25, iss 10 (2020) BASE Show details 2 Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Bigdeli, Tim B; Genovese, Giulio; Georgakopoulos, Penelope... In: Molecular psychiatry, vol 25, iss 10 (2020) BASE Show details 3 Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis. Kuiper, Jonas JW; Setten, Jessica van; Devall, Matthew... In: Human molecular genetics, vol 27, iss 24 (2018) BASE Show details 4 Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Savage, Jeanne E; Jansen, Philip R; Stringer, Sven... In: Nature genetics, vol 50, iss 7 (2018) BASE Show details 5 Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018). Lam, Max; Trampush, Joey W; Yu, Jin... In: Twin research and human genetics : the official journal of the International Society for Twin Studies, vol 21, iss 5 (2018) BASE Show details 6 GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. Trampush, JW; Yang, MLZ; Yu, J... In: Molecular psychiatry, vol 22, iss 3 (2017) BASE Show details 7 Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. Eicher, John D; Montgomery, Angela M; Akshoomoff, Natacha... In: Brain imaging and behavior, vol 10, iss 1 (2016) BASE Show details 8 Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. Eicher, John D; Montgomery, Angela M; Akshoomoff, Natacha... In: Brain imaging and behavior, vol 10, iss 1 (2016) BASE Show details 9 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) BASE Show details 10 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) BASE Show details 11 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) BASE Show details 12 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 BASE Show details 13 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) BASE Show details 14 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) BASE Show details 15 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) BASE Show details 16 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) BASE Show details

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