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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 30 1 Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation. Klusek, Jessica; Fairchild, Amanda; Moser, Carly... In: Journal of neurodevelopmental disorders, vol 14, iss 1 (2022) BASE Show details 2 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 3 Developmental regulation of canonical and small ORF translation from mRNAs Patraquim, Pedro; Mumtaz, Muhammad Ali Shahzad; Pueyo, Jose Ignacio. - : BMC, 2020 BASE Show details 4 Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature. Ansar, M.; Chung, H.L.; Al-Otaibi, A.... In: American journal of human genetics, vol. 105, no. 5, pp. 907-920 (2019) BASE Show details 5 Global genetic differentiation of complex traits shaped by natural selection in humans. Guo, J.; Wu, Y.; Zhu, Z.... In: Nature communications, vol. 9, no. 1, pp. 1865 (2018) BASE Show details 6 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 7 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 8 High-throughput assessment of small open reading frame translation in Drosophila melanogaster Mumtaz, Muhammad Ali Shahzad. - 2016 BASE Show details 9 A novel multi-alignment pipeline for high-throughput sequencing data. Huang, Shunping; Holt, James; Kao, Chia-Yu... In: Database : the journal of biological databases and curation, vol 2014, iss 0 (2014) BASE Show details 10 Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults Alfred, T; Ben-Shlomo, Y; Cooper, R... In: The Journal of Nutrition , 143 (5) 606 -612. (2013) (2013) BASE Show details 11 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 12 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 13 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 14 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 15 Population-level neutral model already explains linguistic patterns. Bentley, RA; Ormerod, P; Shennan, S In: Proc Biol Sci , 278 (1713) pp. 1770-1772. (2011) (2011) BASE Show details 16 Hemiplasy: a new term in the lexicon of phylogenetics. Avise, John C; Robinson, Terence J In: Systematic biology, vol 57, iss 3 (2008) BASE Show details 17 Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Groszer, M; Keays, DA; Deacon, RM... 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 18 The co-evolution of culturally inherited altruistic helping and cultural transmission under random group formation. Lehmann, L.; Feldman, M.W. In: Theoretical Population Biology, vol. 73, no. 4, pp. 506-516 (2008) BASE Show details 19 The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence Mekel-Bobrov, Nitzan; Posthuma, Danielle; Gilbert, Sandra L.. - : Oxford University Press, 2007 BASE Show details 20 APOE ε2-ε4 genotype is a possible risk factor for primary progressive aphasia [6] Acciarri, A.; Masullo, C. (orcid:0000-0001-7798-3410); Bizzarro, A.. - : WILEY-LISS, 2006 BASE Show details Page: 1 2

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