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Neurocognitive Phenotypes and Genetic Dissection of Disorders of Brain and Behavior
被引:14
|作者:
Congdon, Eliza
[1
,2
]
Poldrack, Russell A.
[3
,4
,5
]
Freimer, Nelson B.
[1
,2
]
机构:
[1] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Ctr Neurobehav Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Psychiat, Los Angeles, CA 90095 USA
[3] Univ Texas Austin, Dept Psychol, Austin, TX 78712 USA
[4] Univ Texas Austin, Dept Neurobiol, Austin, TX 78712 USA
[5] Univ Texas Austin, Imaging Res Ctr, Austin, TX 78712 USA
来源:
关键词:
GENOME-WIDE ASSOCIATION;
NEUROIMAGING INITIATIVE ADNI;
EXTENDED PEDIGREE;
WORKING-MEMORY;
NEUROPSYCHIATRIC DISEASE;
PERSONALITY DIMENSIONS;
CANDIDATE GENES;
HERITABILITY;
EXPRESSION;
ALZHEIMERS;
D O I:
10.1016/j.neuron.2010.10.007
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Elucidating the molecular mechanisms underlying quantitative neurocognitive phenotypes will further our understanding of the brain's structural and functional architecture and advance the diagnosis and treatment of the psychiatric disorders that these traits underlie. Although many neurocognitive traits are highly heritable, little progress has been made in identifying genetic variants unequivocally associated with these phenotypes. A major obstacle to such progress is the difficulty in identifying heritable neurocognitive measures that are precisely defined and systematically assessed and represent unambiguous mental constructs, yet are also amenable to the high-throughput phenotyping necessary to obtain adequate power for genetic association studies. In this perspective we compare the current status of genetic investigations of neurocognitive phenotypes to that of other categories of biomedically relevant traits and suggest strategies for genetically dissecting traits that may underlie disorders of brain and behavior.
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页码:218 / 230
页数:13
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