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1
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
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2
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
In: Nature genetics, vol 50, iss 7 (2018)
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3
Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018).
In: Twin research and human genetics : the official journal of the International Society for Twin Studies, vol 21, iss 5 (2018)
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4
Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex
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)
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5
Novel genetic loci associated with hippocampal volume
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)
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6
Novel genetic loci underlying human intracranial volume identified through genome-wide association
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)
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7
Common genetic variants influence human subcortical brain structures.
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)
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8
Mapping Cortical Thickness in Children with 22q11.2 Deletions
Bearden, Carrie E.; van Erp, Theo G.M.; Dutton, Rebecca A.. - : Oxford University Press, 2007
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9
Mapping Cortical Thickness in Children with 22q11.2 Deletions
Bearden, Carrie E.; van Erp, Theo G.M.; Dutton, Rebecca A.. - : Oxford University Press, 2006
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10
Mapping Cortical Thickness in Children with 22q11.2 Deletions
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