2023
Comparison of multiple imputation and other methods for the analysis of imputed genotypes
Auer P, Wang G, Li G, DeWan A, Leal S. Comparison of multiple imputation and other methods for the analysis of imputed genotypes. BMC Genomics 2023, 24: 303. PMID: 37277705, PMCID: PMC10242917, DOI: 10.1186/s12864-023-09415-0.Peer-Reviewed Original Research
2012
Whole-exome sequencing of a pedigree segregating asthma
DeWan AT, Egan KB, Hellenbrand K, Sorrentino K, Pizzoferrato N, Walsh KM, Bracken MB. Whole-exome sequencing of a pedigree segregating asthma. BMC Medical Genomics 2012, 13: 95. PMID: 23046476, PMCID: PMC3563469, DOI: 10.1186/1471-2350-13-95.Peer-Reviewed Original ResearchConceptsNon-asthmatic childrenWhole-exome sequencingAsthma candidate genesAsthmatic childrenAsthmaAsthma associationsAffected motherExome sequencingUnaffected fatherAsthma-susceptibility variantsPrediction scoreUnaffected offspringCommon risk variantsRisk variantsCandidate genesChildrenNonsynonymous variantsAffected offspring
2006
HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration
DeWan A, Liu M, Hartman S, Zhang SS, Liu DT, Zhao C, Tam PO, Chan WM, Lam DS, Snyder M, Barnstable C, Pang CP, Hoh J. HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration. Science 2006, 314: 989-992. PMID: 17053108, DOI: 10.1126/science.1133807.Peer-Reviewed Original ResearchMeSH KeywordsAgedAged, 80 and overAgingAsian PeopleChromatin ImmunoprecipitationChromosomes, Human, Pair 10FemaleGenetic Predisposition to DiseaseGenotypeHeLa CellsHigh-Temperature Requirement A Serine Peptidase 1HumansLinkage DisequilibriumMacular DegenerationMaleMiddle AgedPolymorphism, Single NucleotidePromoter Regions, GeneticRetinal NeovascularizationSerine EndopeptidasesSerum Response FactorTranscription Factor AP-2ConceptsAssociation mapping strategySerine protease genesSingle nucleotide polymorphismsHTRA1 promoter polymorphismPromoter regionProtease geneChromosome 10q26H geneRisk-associated genotypesGenesGenetic risk factorsMajor genetic risk factorWild-type genotypeFactor H genePolymorphismGenotypesMapping strategyComplement factor H (CFH) genePromoter polymorphismHtrA1Age-related macular degeneration
2001
Linkage of Left Ventricular Contractility to Chromosome 11 in Humans
Arnett D, Devereux R, Kitzman D, Oberman A, Hopkins P, Atwood L, Dewan A, Rao DC. Linkage of Left Ventricular Contractility to Chromosome 11 in Humans. Hypertension 2001, 38: 767-772. PMID: 11641284, DOI: 10.1161/hy1001.092650.Peer-Reviewed Original ResearchMeSH KeywordsBlack PeopleChromosome MappingChromosomes, Human, Pair 11Chromosomes, Human, Pair 12Chromosomes, Human, Pair 22EchocardiographyFemaleGenetic LinkageGenome, HumanGenotypeHeart VentriclesHumansHypertensionLod ScoreMaleMicrosatellite RepeatsMiddle AgedMyocardial ContractionPhenotypeQuantitative Trait, HeritableWhite PeopleConceptsCongestive heart failureLV contractilityHeart failureVentricular contractilityMyocardial contractilityImpaired LV contractilityLeft ventricular contractilityAge 60 yearsHypertension Genetic Epidemiology NetworkGenetic Epidemiology NetworkBiethnic sampleCardiovascular deathContractile impairmentFamilial hypertrophic cardiomyopathyMean ageEchocardiographic measurementsHypertrophic cardiomyopathyHypertensive siblingsContractilityEpidemiology NetworkMajor causeSusceptibility genesAgeEthnic groupsSuggestive evidence
2000
A Genome Scan for Renal Function among Hypertensives: the HyperGEN Study
DeWan A, Arnett D, Atwood L, Province M, Lewis C, Hunt S, Eckfeldt J. A Genome Scan for Renal Function among Hypertensives: the HyperGEN Study. American Journal Of Human Genetics 2000, 68: 136-144. PMID: 11115379, PMCID: PMC1234906, DOI: 10.1086/316927.Peer-Reviewed Original ResearchMeSH KeywordsBlack or African AmericanBlack PeopleBody Mass IndexChromosomes, Human, Pair 1Chromosomes, Human, Pair 3Chromosomes, Human, Pair 6CreatineFemaleGenotypeHumansHypertensionKidneyKidney Function TestsLod ScoreMaleMiddle AgedModels, GeneticNuclear FamilyPhenotypeQuantitative Trait, HeritableSoftwareWhite PeopleConceptsCreatinine clearanceRenal functionAfrican American subjectsWhite subjectsHypertension Genetic Epidemiology Network (HyperGEN) studyLarge biracial sampleResidual creatinine clearanceComplications of hypertensionCreatinine clearance measurementsGood evidenceHypertensive individualsKidney functionMean ageAmerican subjectsBiracial sampleHypertensive siblingsApolipoprotein DHyperGEN studyClearanceClearance measurementsHypertensionCandidate genesSpecific genetic regionsUnderlying genetic componentSubjects