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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 27 1 Genetic Structure of IQ, Phonemic Decoding Skill, and Academic Achievement Lazaroo, Nikita K.; Bates, Timothy C.; Hansell, Narelle K.. - : Frontiers Media S.A., 2019 BASE Show details 2 Genetic structure of IQ, phonemic decoding skill, and academic achievement Lazaroo, Nikita K.; Bates, Timothy C.; Hansell, Narelle K.. - : Frontiers Research Foundation, 2019 BASE Show details 3 Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex Guadalupe, Tulio; Mathias, Samuel R.; vanErp, Theo G. M.... In: ISSN: 1931-7557 ; EISSN: 1931-7565 ; Brain imaging and behavior (Brain Imaging Behav) ; https://hal.archives-ouvertes.fr/hal-01382787 ; Brain imaging and behavior (Brain Imaging Behav), Secaucus, NJ : Springer, 2017, 11 (5), pp.1497-1514. ⟨10.1007/s11682-016-9629-z⟩ (2017) BASE Show details 4 Novel genetic loci associated with hippocampal volume Hibar, Derrek P.; Adams, Hieab H. H.; Jahanshad, Neda... In: ISSN: 2041-1723 ; EISSN: 2041-1723 ; Nature Communications ; https://hal.archives-ouvertes.fr/hal-01488337 ; Nature Communications, Nature Publishing Group, 2017, 8, pp.13624. ⟨10.1038/ncomms13624⟩ (2017) BASE Show details 5 Novel genetic loci underlying human intracranial volume identified through genome-wide association Adams, Hieab H H; Hibar, Derrek P; Chouraki, Vincent... In: ISSN: 1097-6256 ; EISSN: 1546-1726 ; Nature Neuroscience ; https://hal.archives-ouvertes.fr/hal-01382716 ; Nature Neuroscience, Nature Publishing Group, 2016, 19 (12), pp.1569-1582. ⟨10.1038/nn.4398⟩ (2016) BASE Show details 6 Common genetic variants influence human subcortical brain structures. Hibar, Derrek P; Stein, Jason L; Renteria, Miguel E... In: ISSN: 0028-0836 ; EISSN: 1476-4679 ; Nature ; https://hal.archives-ouvertes.fr/hal-01196805 ; Nature, Nature Publishing Group, 2015, 520 (7546), pp.224-9. ⟨10.1038/nature14101⟩ (2015) BASE Show details 7 Genome-wide screening for DNA variants associated with reading and language traits Gialluisi, Alessandro; Newbury, Dianne F; Wilcutt, Erik G. - 2015 BASE Show details 8 The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data Thompson, Paul,; Stein, Jason,; Medland, Sarah... In: ISSN: 1931-7557 ; EISSN: 1931-7565 ; Brain imaging and behavior (Brain Imaging Behav) ; https://hal-pasteur.archives-ouvertes.fr/pasteur-01967166 ; Brain imaging and behavior (Brain Imaging Behav), Secaucus, NJ : Springer, 2014, 8 (2), pp.152-182. ⟨10.1007/s11682-013-9269-5⟩ (2014) BASE Show details 9 Molecular genetic contributions to socioeconomic status and intelligence Marioni, Riccardo E.; Davies, Gail; Hayward, Caroline. - : Elsevier Ltd, 2014 BASE Show details 10 Genetic Copy Number Variation and General Cognitive Ability MacLeod, Andrew K.; Davies, Gail; Payton, Antony. - : Public Library of Science, 2012 BASE Show details 11 Genetic contributions to stability and change in intelligence from childhood to old age Deary, Ian J.; Yang, Jian; Davies, Gail. - : Nature Publishing Group, 2012 BASE Show details 12 Genome-wide association studies establish that human intelligence is highly heritable and polygenic Davies, Gail; Tenesa, Albert; Payton, Antony. - 2011 BASE Show details 13 Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits Bates, Timothy C.; Luciano, Michelle; Medland, Sarah E.. - : Springer, 2011 BASE Show details 14 Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample Lind, Penelope A; Luciano, Michelle; Wright, Margaret J. - : Nature Publishing Group, 2010 BASE Show details 15 Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample Lind, Penelope A.; Luciano, Michelle; Wright, Margaret J.. - : Nature Publishing Group, 2010 BASE Show details 16 Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficits Bates, Timothy C.; Luciano, Michelle; Montgomery, Grant W.. - : Springer New York LLC, 2010 BASE Show details 17 Genetic and environmental bases of reading and spelling : a unified genetic dual route model Luciano, Michelle; Martin, Nicholas G.; Castles, Anne... In: Reading and writing. - New York, NY : Springer Science+Business Media 20 (2007) 1-2, 147-171 BLLDB OLC Linguistik Show details 18 Genetic and environmental bases of reading and spelling : a unified genetic dual route model Bates, Timothy C; Castles, Anne; Luciano, Michelle. - : Springer Netherlands, 2007 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.; Lind, Penelope; Gosso, M. Florencia; Luciano, Michelle; Harris, Sarah E.; Bates, Timothy C.; Polderman, Tinca J.; Whalley, Lawrence J.; Fox, Helen; Starr, John M.; Evans, Patrick D.; Montgomery, Grant W.; Fernandes, Croydon; Heutink, Peter; Martin, Nicholas G.; Boomsma, Dorret I.; Deary, Ian J.; Wright, Margaret J.; de Geus, Eco J.; Lahn, Bruce T.. - : Oxford University Press, 2007 Abstract: Recent studies have made great strides towards identifying putative genetic events underlying the evolution of the human brain and its emergent cognitive capacities. One of the most intriguing findings is the recurrent identification of adaptive evolution in genes associated with primary microcephaly, a developmental disorder characterized by severe reduction in brain size and intelligence, reminiscent of the early hominid condition. This has led to the hypothesis that the adaptive evolution of these genes has contributed to the emergence of modern human cognition. As with other candidate loci, however, this hypothesis remains speculative due to the current lack of methodologies for characterizing the evolutionary function of these genes in humans. Two primary microcephaly genes, ASPM and Microcephalin, have been implicated not only in the adaptive evolution of the lineage leading to humans, but in ongoing selective sweeps in modern humans as well. The presence of both the putatively adaptive and neutral alleles at these loci provides a unique opportunity for using normal trait variation within humans to test the hypothesis that the recent selective sweeps are driven by an advantage in cognitive abilities. Here, we report a large-scale association study between the adaptive alleles of these genes and normal variation in several measures of IQ. Five independent samples were used, totaling 2393 subjects, including both family-based and population-based datasets. Our overall findings do not support a detectable association between the recent adaptive evolution of either ASPM or Microcephalin and changes in IQ. As we enter the post-genomic era, with the number of candidate loci underlying human evolution growing rapidly, our findings highlight the importance of direct experimental validation in elucidating their evolutionary role in shaping the human phenotype. Keyword: 321011 Medical Genetics; 730107 Inherited diseases (incl. gene therapy); Adolescent; Adult; Alleles; C1; Child URL: https://espace.library.uq.edu.au/view/UQ:131445 BASE Hide details 20 Genetic and environmental bases of reading and spelling: a unified genetic dual route model Bates, Timothy C.; Castles, Anne; Luciano, Michelle. - : Springer Netherlands, 2007 BASE Show details Page: 1 2

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