课题基金 / 基金详情

Genetics of Brain Structure and Function

Genetics of Brain Structure and Function
大脑结构和功能的遗传学
批准号:
7263881
负责人:
DAVID C GLAHN
金额:
$62.78万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-08-01 至 2011-07-31
关键词:
AffectAnatomyAnxiety DisordersArchitectureAttention deficit hyperactivity disorderAutistic DisorderBase of the BrainBiocompatible MaterialsBioinformaticsBiologicalBiologyBiomedical ResearchBrainBrain DiseasesBrain imagingCandidate Disease GeneChromosome MappingCommunitiesComplexComputer SimulationDNA ResequencingDataData CorrelationsDementiaDevelopmentDiabetes MellitusDiseaseDisruptionDissectionEconomic BurdenEpilepsyEvaluationExhibitsExtended FamilyFacility Construction Funding CategoryFamilyFoundationsFoxesFundingFutureGene ExpressionGenesGeneticGenetic DeterminismGenetic ResearchGenomeGenome ScanGenomicsGenotypeGoalsHealth SciencesHeart DiseasesHeritabilityHumanHuman GeneticsIndividualIndividual DifferencesInterventionJointsLeadLeukocytesLinkLocalizedMagnetic Resonance ImagingMeasurableMeasurementMeasuresMental disordersMethodsMexican AmericansMissionModelingMolecular AnalysisMood DisordersMorbidity - disease rateNational Institute of Mental HealthNeurocognitiveNeurologicNeurosciencesNoiseNucleotidesNumbersOsteoporosisParticipantPathologyPhenotypePositioning AttributeProceduresPsyche structurePublic HealthQualifyingQuantitative GeneticsQuantitative Trait LociRateRelative (related person)ResearchResearch DesignResearch PersonnelResource SharingResourcesReverse Transcriptase Polymerase Chain ReactionRiskSamplingSchizophreniaShort Tandem Repeat PolymorphismSignal TransductionSingle Nucleotide PolymorphismSourceStructureSusceptibility GeneTestingTexasTherapeuticUncertaintyUniversitiesVariantaddictionaffectionbasecost effectivedisorder riskendophenotypegene discoverygenetic analysisgenetic pedigreegenetic resourcegenome-wide linkageimprovedin vivoindexingmembermortalityneuroimagingneuropsychologicalnovelnovel diagnosticsprogramsresearch studytraittranscriptomics

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DESCRIPTION (provided by applicant): The goal of this project is to identify quantitative trait loci associated with variation in brain structure and function. The ultimate promise of this research is the discovery of genes that predispose to brain disorders and mental illnesses. We believe that the analysis of genetic influences on brain structure and function in randomly sampled extended pedigrees will provide significant clues regarding the genes that are involved in both normal and pathological brain function. The focus of the project is on the genetic dissection of quantitative endophenotypes that more directly index the underlying biological basis of brain function than do discrete disease states themselves. To this end, we will perform neuroimaging and conduct neuropsychological examinations on Mexican American individuals who have been part of our ongoing genetic research studies for the past 15 years. All participants were previously genotyped and our plan is to utilize existing genome scan and genome-wide quantitative transcriptomic data for correlation with neuroanatomic and neurocognitive variables. Our specific aims are to: 1) perform high quality brain magnetic resonance imaging and neuropsychological examinations on 1,000 Mexican Americans who are members of approximately 30 large extended families, 2) assess the quantitative genetic architecture of brain-related phenotypes by estimating their heritabilities and their genetic correlations, 3) classify specific brain morphological variables and quantitative leukocyte-derived gene expression measures as endophenotypes related to brain function, 4) localize QTLs influencing variation in the quantitative brain-related phenotypes by performing linkage-based genome scanning using the variance component method, 5) refine the position of localized QTLs and identify positional candidate loci using an objective prioritization strategy that jointly utilizes in silico bioinformatics, genetic, and transcriptional data, and 6) identify the most likely functional variations within the two best positional candidate genes. This project involves coordinated R01 applications from Dr. John Blangero, Southwest Foundation for Biomedical Research, and Drs. David Glahn and Peter Fox, University of Texas Health Science Center at San Antonio. If funded, our data and biomaterials will be incorporated into the NIMH Human Genetics Initiative making them available to qualified researchers in the wider scientific community. Relevance to agency mission: Brain-related mental diseases are a major public health burden whose biology is still largely unknown. By identifying genes involved in brain function and structure, we will provide novel biological candidates for the determinants of such diseases and thus improve potential for intervention.
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Translational Post-doctoral Training in Neurodevelopment
  • 批准号:
    10411050
  • 项目类别:
  • 资助金额:
    $19.37万
  • 财政年份:
    2017
  • 负责人:
    DAVID C GLAHN
  • 依托单位:
Translational Post-doctoral Training in Neurodevelopment
  • 批准号:
    10650880
  • 项目类别:
  • 资助金额:
    $29.15万
  • 财政年份:
    2017
  • 负责人:
    DAVID C GLAHN
  • 依托单位:
1/3:Pedigree-Based Whole Genome Sequencing of Affective and Psychotic Disorders
  • 批准号:
    9228398
  • 项目类别:
  • 资助金额:
    $36.38万
  • 财政年份:
    2015
  • 负责人:
    DAVID C GLAHN
  • 依托单位:
1/3:Pedigree-Based Whole Genome Sequencing of Affective and Psychotic Disorders
  • 批准号:
    9024625
  • 项目类别:
  • 资助金额:
    $28.2万
  • 财政年份:
    2015
  • 负责人:
    DAVID C GLAHN
  • 依托单位:
海外基金