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Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation.
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In: Journal of neurodevelopmental disorders, vol 14, iss 1 (2022)
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The trans-ancestral genomic architecture of glycemic traits.
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In: Nature genetics, vol. 53, no. 6, pp. 840-860 (2021)
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Developmental regulation of canonical and small ORF translation from mRNAs
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Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
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In: American journal of human genetics, vol. 105, no. 5, pp. 907-920 (2019)
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Global genetic differentiation of complex traits shaped by natural selection in humans.
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In: Nature communications, vol. 9, no. 1, pp. 1865 (2018)
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Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.
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In: Genetics in medicine, vol. 20, no. 7, pp. 778-784 (2018)
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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
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In: Molecular psychiatry, vol 22, iss 3 (2017)
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High-throughput assessment of small open reading frame translation in Drosophila melanogaster
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A novel multi-alignment pipeline for high-throughput sequencing data.
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In: Database : the journal of biological databases and curation, vol 2014, iss 0 (2014)
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Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults
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In: The Journal of Nutrition , 143 (5) 606 -612. (2013) (2013)
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Individual common variants exert weak effects on the risk for autism spectrum disorders.
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In: Human molecular genetics, vol 21, iss 21 (2012)
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Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
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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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Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
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In: PLoS genetics, vol 7, iss 7 (2011)
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Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
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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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Population-level neutral model already explains linguistic patterns.
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In: Proc Biol Sci , 278 (1713) pp. 1770-1772. (2011) (2011)
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Hemiplasy: a new term in the lexicon of phylogenetics.
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In: Systematic biology, vol 57, iss 3 (2008)
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Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
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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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The co-evolution of culturally inherited altruistic helping and cultural transmission under random group formation.
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In: Theoretical Population Biology, vol. 73, no. 4, pp. 506-516 (2008)
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The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence
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APOE ε2-ε4 genotype is a possible risk factor for primary progressive aphasia [6]
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