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COLLABORATIVE STUDY ON THE GENETICS OF ALCOHOLISM/COGA

COLLABORATIVE STUDY ON THE GENETICS OF ALCOHOLISM/COGA
酗酒/COGA 遗传学合作研究
批准号:
7493525
负责人:
BERNICE PORJESZ
金额:
$661.74万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-09-29 至 2009-08-31
关键词:
AdolescentAffectAgeAgreementAlcohol PhenotypeAlcohol dependenceAlcohol or Other Drugs useAlcoholismAlcoholsAntisocial Personality DisorderArtsAttention deficit hyperactivity disorderBehavioralBeliefBiologicalBlood specimenBrainCandidate Disease GeneCell LineCellsCharacteristicsClinicalClinical assessmentsCodeCognitiveCollaborationsComplexConditionConduct DisorderCore FacilityCoupledDNADataData SetDatabasesDependenceDerivation procedureDevelopmentDiagnosisDiseaseDisease OutcomeDisinhibitionDrug AddictionDrug usageEducational workshopElectroencephalogramEnvironmentEnvironmental Risk FactorEthanolEventEvent-Related PotentialsFamilyFamily StudyFrequenciesFunctional disorderGenesGeneticGenetic MaterialsGenetic Predisposition to DiseaseGenome ScanGenotypeGoalsHaplotypesHeavy DrinkingHourHousingImpulsivityIndividualInterviewKnowledgeLaboratoriesLeadLinkage DisequilibriumLinkage Disequilibrium MappingLocalizedMeasuresMental DepressionMetabolicMethodsMiningMood DisordersNational Institute on Alcohol Abuse and AlcoholismNeuropsychological TestsNicotine DependenceNumbersOnset of illnessOppositional Defiant DisorderOutcomePathway interactionsPhenotypePopulationPre-studyPredispositionPrevention approachPrincipal InvestigatorProspective StudiesPsychopathologyPublic HealthQualifyingQuantitative GeneticsRNA SplicingRangeReceptor GeneResearchResearch PersonnelResourcesRestRiskRoleSamplingScienceScientistScoreSecondary PreventionSeveritiesSingle Nucleotide PolymorphismSiteSmokingSourceStatistical MethodsSubstance Abuse, OtherSubstance AddictionSubstance-Related DisordersSymptomsTestingTimeTime StudyVariantWorkaddictionalcohol abuse therapyalcohol related problembaseclinical phenotypedata managementdrinkingendophenotypeexpectationfollow-upfrontal lobefrontal lobe functiongene environment interactiongenetic analysisgenetic linkagegenome-wide linkageimprovedinnovationmembermultidisciplinaryneuromechanismneurophysiologyneuropsychologicalnovelnovel strategiesproblem drinkerprogramspromoterrelating to nervous systemrepositoryskillssuccesssuicidal behaviortooltraityoung adult

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DESCRIPTION (provided by applicant): Alcoholism is a complex disease influenced by genetic susceptibility, environmental factors, and by interactions among genes and between genes and environment. This proposal is for a five-year renewal of the Collaborative Study on the Genetics of Alcoholism (COGA), an eight-site national collaboration with the overarching goal of identifying and characterizing genes that affect the susceptibility to develop alcohol dependence and related phenotypes. This renewal is based on the hypothesis that some of the genetically influenced differences in susceptibility are unique to alcoholism, whereas others, involving frontal lobe function (impulsivity, neural disinhibition) influence a range of related outcomes including externalizing and mood disorders and abuse of other substances. COGA has identified several genes that influence the development of alcoholism and it's correlated phenotypes, including endophenotypes reflecting basic neural mechanisms. We propose to build on our successful strategies that combine the development of neurophysiological and clinical/behavioral henotypes with extensive SNP genotyping and linkage disequilibrium analyses to identify genes underlying those phenotypes and examine mechanisms by which they influence the phenotypes. Functional studies of genes strongly associated with important phenotypes, including examination of potential coding and splicing differences and potential differences in promoter function will be conducted. A prospective study of adolescents and young adults is also proposed in which novel neurophysiological and other phenotypes will be measured and subject to genetic analyses. This will facilitate further understanding of the role of specific genes and how they interact with each other and with the environment to influence the time course of development of alcoholism and related phenotypes. These components are interrelated, and all contribute to the theme of identifying and understanding genetic and environmental factors that affect alcoholism and related phenotypes, with the expectation that this knowledge will suggest novel approaches to prevention and treatment of alcoholism and related disorders.
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NEUROPHYSIOLOGICAL PHENOTYPIC MARKERS OF RISK
  • 批准号:
    6347160
  • 项目类别:
  • 资助金额:
    $99.97万
  • 财政年份:
    2000
  • 负责人:
    BERNICE PORJESZ
  • 依托单位:
NEUROPHYSIOLOGICAL PHENOTYPIC MARKERS OF RISK
  • 批准号:
    6299176
  • 项目类别:
  • 资助金额:
    $99.97万
  • 财政年份:
    2000
  • 负责人:
    BERNICE PORJESZ
  • 依托单位:
IRPG1 R01 NOVEL PHENOTYPES FOR THE GENETIC ANALYSIS
  • 批准号:
    6604025
  • 项目类别:
  • 资助金额:
    $64.17万
  • 财政年份:
    1999
  • 负责人:
    BERNICE PORJESZ
  • 依托单位:
CORE--NEUROPHYSIOLOGICAL PHENOTYPIC MARKERS OF RISK
  • 批准号:
    6097690
  • 项目类别:
  • 资助金额:
    $65.93万
  • 财政年份:
    1998
  • 负责人:
    BERNICE PORJESZ
  • 依托单位:
海外基金