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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 34 1 Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders Devanna, P; Chen, X S; Ho, J. - 2021 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 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 4 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 5 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 6 Cortical responses before 6 months of life associate with later autism. ... Lloyd-Fox, Sarah; Blasi, A; Pasco, G. - : Apollo - University of Cambridge Repository, 2018 BASE Show details 7 Cortical responses before 6 months of life associate with later autism. Lloyd-Fox, Sarah; Blasi, A; Pasco, G. - : Wiley, 2018. : Eur J Neurosci, 2018 BASE Show details 8 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 9 Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. Leppa, Virpi M; Kravitz, Stephanie N; Martin, Christa Lese... In: American journal of human genetics, vol 99, iss 3 (2016) BASE Show details 10 Differential susceptibility to effects of maternal sensitivity? A study of candidate plasticity genes. Belsky, Jay; Newman, Daniel A; Widaman, Keith F... In: Development and psychopathology, vol 27, iss 3 (2015) BASE Show details 11 Acculturation, Behavioral Factors, and Family History of Breast Cancer among Mexican and Mexican-American Women. Nodora, Jesse N; Cooper, Renee; Talavera, Gregory A... In: Women's health issues : official publication of the Jacobs Institute of Women's Health, vol 25, iss 5 (2015) BASE Show details 12 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) BASE Show details 13 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) BASE Show details 14 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 15 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 16 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 17 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) BASE Show details 18 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 19 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 20 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 Page: 1 2

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