Epigenetics and disease: the role of DNA methylation in schizophrenia susceptibil
Epigenetics and disease: the role of DNA methylation in schizophrenia susceptibil
批准号:
8521226
负责人:
Roel A Ophoff
金额:
$48.51万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2015-08-31
关键词:
AffectAgeApplications GrantsBase SequenceBiochemicalBrainBrain regionChromosome StructuresComplexDNADNA MethylationDNA SequenceDNA StructureDiagnosisDiseaseDisease susceptibilityDrug TargetingEpigenetic ProcessGenderGenesGeneticGenomicsHeritabilityHuman GenomeIndividual DifferencesLeadMental disordersModificationMolecularMutationPathway interactionsPatientsPhasePlayPopulationPredispositionRelative (related person)RoleSamplingSchizophreniaSignal TransductionSiteSocietiesTissuesTwin Multiple BirthValidationbaseburden of illnesscohortcomparativedisorder preventiongenome wide association studygenome-wideimprovedinsightneuropsychiatryperipheral bloodsocioeconomicstrait
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Most psychiatric disorders are not due to mutations in a single gene but rather involve cellular pathways under control of many genes and molecular signals. Recent studies point to the fact that complex epigenetic mechanisms regulating gene activity 'above' the genetic nucleotide sequence may be involved as well. The best understood mechanism of epigenetic modification is DNA methylation. In this genome-wide study we will examine the role of DNA methylation in schizophrenia susceptibility. Our study consists of a genome-wide discovery and replication phase to identify CpG loci in the human genome that are under epigenetic control and involved in disease susceptibility, followed by locus-specific validation in large schizophrenia cohorts. Our systematic approach for identifying candidate CpG loci involved in disease also includes study of general features of DNA methylation such as age, gender and genetic controls. The genome-wide effort with comparative analyses of multiple brain regions of patients and controls will provide a unique opportunity to establish what role DNA methylation plays in vulnerability to develop schizophrenia and perhaps other psychiatric traits.
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Exposure to cyanobacteria and BMAA in ALS through the gut environment microbiome
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Exposure to cyanobacteria and BMAA in ALS through the gut environment microbiome
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Parental Age and Schizophrenia Susceptibility
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Parental Age and Schizophrenia Susceptibility
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Rare Coding Variants at Microdeletion Regions and Schizophrenia Susceptibility
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财政年份:2011
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Rare Coding Variants at Microdeletion Regions and Schizophrenia Susceptibility
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Genomic Studies of Bipolar Disorder in a Large Cohort from The Netherlands
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依托单位:
Genomic Studies of Bipolar Disorder in a Large Cohort from The Netherlands
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资助金额:$141.59万
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财政年份:2010
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依托单位:
Genomic Studies of Bipolar Disorder in a Large Cohort from The Netherlands
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项目类别:
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依托单位:
Genomic Studies of Bipolar Disorder in a Large Cohort from The Netherlands
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资助金额:$81.52万
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财政年份:2010
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依托单位:
Epigenetics and disease: the role of DNA methylation in schizophrenia susceptibil
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批准号:8304339
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项目类别:
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资助金额:$50.35万
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财政年份:2009
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负责人:Roel A Ophoff
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依托单位:
Epigenetics and disease: the role of DNA methylation in schizophrenia susceptibil
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批准号:7931944
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项目类别:
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资助金额:$50.5万
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财政年份:2009
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负责人:Roel A Ophoff
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依托单位:
Epigenetics and disease: the role of DNA methylation in schizophrenia susceptibil
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批准号:7726401
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项目类别:
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资助金额:$49.99万
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依托单位:
Epigenetics and disease: the role of DNA methylation in schizophrenia susceptibil
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资助金额:$50.42万
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依托单位:
Genetics of Gene Expression and Gene Mapping for Amytrophic Lateral Sclerosis
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项目类别:
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依托单位:
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项目类别:
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资助金额:$31.36万
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财政年份:2008
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负责人:Roel A Ophoff
-
依托单位:
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