grant

Comprehensive computational analysis of genetic and regulatory differences between individuals with African and European ancestries across four brain regions

Organization NORTHWESTERN UNIVERSITYLocation CHICAGO, UNITED STATESPosted 1 Dec 2021Deadline 31 Mar 2027
NIHUS FederalResearch GrantFY2025Accuracy of DiagnosisActive Follow-upAddressAffectAfrican ancestryAfrican descentAmmon HornAntipsychotic AgentsAntipsychotic DrugsAntipsychoticsAutopsyBS-seqBisulfite-based sequencingBrainBrain DiseasesBrain DisordersBrain Nervous SystemBrain regionCareer Transition AwardCell BodyCellsCollaborationsCollectionComplexComputer AnalysisCornu AmmonisDNA MethylationDataData SetDecrease health disparitiesDentate FasciaDevelopmentDiathesisDiseaseDisease susceptibilityDisorderDisparitiesDisparityEncephalonEncephalon DiseasesEnvironmentEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessEquityEuropean ancestryExonsExplosionFascia DentataFutureGene TranscriptionGenesGeneticGenetic DiversityGenetic TranscriptionGenetic VariationGenomicsGenotypeGoalsGrantGyrus DentatusHealth disparity mitigationHealth disparity reductionHeritabilityHippocampusHumanHuman GeneticsIndividualIntracranial CNS DisordersIntracranial Central Nervous System DisordersInvestigatorsLifeLinkLower health disparitiesMachine LearningMajor TranquilizersMajor Tranquilizing AgentsMapsMental HealthMental HygieneMental disordersMental health disordersMentorsMentorshipMethodsMethylationMitigate health disparitiesModelingModern ManNervous System DiseasesNervous System DisorderNeural DevelopmentNeuroleptic AgentsNeuroleptic DrugsNeurolepticsNeurologic DisordersNeurological DisordersNeurosciencesNucleus CaudatusPhasePlayPostdocPostdoctoral FellowPrefrontal CortexPsychiatric DiseasePsychiatric DisorderPsychological HealthQTLQuantitative Trait LociR-Series Research ProjectsR01 MechanismR01 ProgramRNA ExpressionRNA SeqRNA sequencingRNAseqReduce health disparitiesResearchResearch AssociateResearch GrantsResearch PersonnelResearch Project GrantsResearch ProjectsResearchersResource DevelopmentRoleSNP arraySNP chipSamplingSchizophreniaSchizophrenic DisordersStatistical MethodsTechniquesTestingTrainingTranscriptTranscriptionUniversitiesVariantVariationWorkactive followupbiological researchbisulfite sequencingbisulfite-seqbrain tissuecareercareer developmentcaudate nucleuscausal allelecausal genecausal mutationcausal variantcausative mutationcausative variantcell typecohortcomputational analysescomputational analysiscomputer analysesdata integrationdementia praecoxdentate gyrusdevelopmentaldiagnostic accuracydifferential expressiondifferentially expresseddisparity in healthdrug discoveryentire genomeepigenetic variationepigeneticallyexperienceexperimentexperimental researchexperimental studyexperimentsfetalfollow upfollow-upfollowed upfollowupfull genomegenetic analysisgenomic datagenomic datasethealth disparityhippocampalimprovedindexingliability to diseasemachine based learningmental illnessnecropsyneurodevelopmentneurological diseaseneuropsychiatric diseaseneuropsychiatric disorderpersonalization of treatmentpersonalized medicinepersonalized therapypersonalized treatmentpost-docpost-doctoralpost-doctoral traineepostmortempostnatalprenatalpsychiatric illnesspsychological disorderresearch associatesresponseschizophrenicsingle nucleotide polymorphism arraysingle nucleotide polymorphism chipskillssocial rolestatistic methodssuccesstraittranscriptional differencestranscriptome sequencingtranscriptomic sequencingunbornwhole genome
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Full Description

Project Summary / Abstract
Health disparities have endured for centuries. The disparity in research for biological variations is even greater,

where the explosion of genetic and environmental data has focused almost exclusively on those of European

ancestry (EA). In neuroscience and genomics, individuals with recent African ancestry (AA) account for less

than 5% of large-scale genomic studies but are 20% more likely to experience a major mental health crisis. To

compound this issue further, studies have linked genetic differences between AA and EA for divergent

responses to antipsychotics. As a result, large-scale studies for neuropsychiatric disorders have limited

diagnostic accuracy for non-European ancestry individuals, hindering the development of effective equitable

neurotherapeutics and potentially increasing health disparities. Despite the clear urgent need, there are no

large-scale studies examining genetic or regulatory differences between AA and EA in the human brain. This

proposal seeks to address this gap in research by comparing AA with well-studied EA individuals. The initial

goal of this proposal is to identify genetic and regulatory difference between AA (n=784) and EA (n=678) in

postmortem caudate nucleus (n=420), dentate gyrus (n=161), dorsolateral prefrontal cortex (n=434), and

hippocampus (n=447), compiled from one of the largest postmortem brain collections of psychiatric disorders.

This diverse large-scale postmortem brain tissue will allow us to test the hypotheses of genetic variations

influence on brain region-specific transcriptional and epigenetic changes for ancestry across prenatal and

postnatal life. This MOSAIC (Maximizing Opportunities for Scientific and Academic Independent Careers)

Postdoctoral Career Transition Award to Promote Diversity will be supported by excellent career development

resources at the Lieber Institute for Brain Development and Johns Hopkins University, and training from a

mentoring team of globally recognized experts in the fields of human genetics and advanced statistical

methods. It will provide a first of its kind examination of ancestry in neuroscience, which will advance our

understanding of genetic variation in the human brain.

Grant Number: 5R00MD016964-04
NIH Institute/Center: NIH

Principal Investigator: Kynon Benjamin

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