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1.
Twin Res Hum Genet ; 15(3): 414-8, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22856375

ABSTRACT

In an attempt to increase power to detect genetic associations with brain phenotypes derived from human neuroimaging data, we recently conducted a large-scale, genome-wide association meta-analysis of hippocampal, brain, and intracranial volume through the Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) consortium. Here, we present a freely available online interactive tool, EnigmaVis, which makes it easy to visualize the association results generated by the consortium alongside allele frequency, genes, and functional annotations. EnigmaVis runs natively within the web browser, and generates plots that show the level of association between brain phenotypes at user-specified genomic positions. Uniquely, EnigmaVis is dynamic; users can interact with elements on the plot in real time. This software will be useful when exploring the effect on brain structure of particular genetic variants influencing neuropsychiatric illness and cognitive function. Future projects of the consortium and updates to EnigmaVis will also be displayed on the site. EnigmaVis is freely available online at http://enigma.loni.ucla.edu/enigma-vis/


Subject(s)
Brain/anatomy & histology , Brain/physiology , Databases, Genetic , Genome-Wide Association Study , Internet , Neuroimaging , Humans , Meta-Analysis as Topic , Phenotype
2.
Trends Cogn Sci ; 15(9): 428-35, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21816658

ABSTRACT

Cognitive impairments are central to schizophrenia and could mark underlying biological dysfunction but efforts to detect genetic associations for schizophrenia or cognitive phenotypes have been disappointing. Phenomics strategies emphasizing simultaneous study of multiple phenotypes across biological scales might help, particularly if the high heritabilities of schizophrenia and cognitive impairments are due to large numbers of genetic variants with small effect. Convergent evidence is reviewed, and a new collaborative knowledgebase - CogGene - is introduced to share data about genetic associations with cognitive phenotypes, and enable users to meta-analyze results interactively. CogGene data demonstrate the need for larger studies with broader representation of cognitive phenotypes. Given that meta-analyses will probably be necessary to detect the small association signals linking the genome and cognitive phenotypes, CogGene or similar applications will be needed to enable collaborative knowledge aggregation and specify true effects.


Subject(s)
Cognition Disorders/genetics , Genetic Predisposition to Disease/genetics , Genome-Wide Association Study , Phenotype , Cognition Disorders/etiology , Humans , Schizophrenia/complications , Schizophrenia/genetics
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