Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics.
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Genes to diseases (G2D) computational method to identify asthma candidate genesVariants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitisAsthma and genes encoding components of the vitamin D pathwayDCDC2 is associated with reading disability and modulates neuronal development in the brain.Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autismThe BTNL2 gene and sarcoidosis susceptibility in African Americans and WhitesInvestigation of autism and GABA receptor subunit genes in multiple ethnic groupsVariant of TYR and autoimmunity susceptibility loci in generalized vitiligoCandidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for cleftsFindings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohortT-bet polymorphisms are associated with asthma and airway hyperresponsivenessInteraction between interleukin 3 and dystrobrevin-binding protein 1 in schizophreniaAbnormal melatonin synthesis in autism spectrum disordersThe neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer diseaseA genetic variant that disrupts MET transcription is associated with autismSecreted modular calcium-binding protein 2 haplotypes are associated with pulmonary functionInvolvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expressionLinkage and association studies in African- and Caucasian-American populations demonstrate that SHC3 is a novel susceptibility locus for nicotine dependenceAnalysis of the RELN gene as a genetic risk factor for autismSystematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of KosraeEthnic-specific genetic association of variants in the corticotropin-releasing hormone receptor 1 gene with nicotine dependence.Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populationsSerotonin transporter and receptor genes significantly impact nicotine dependence through genetic interactions in both European American and African American smokersAssociation and interaction analysis of variants in CHRNA5/CHRNA3/CHRNB4 gene cluster with nicotine dependence in African and European AmericansConvergent evidence that choline acetyltransferase gene variation is associated with prospective smoking cessation and nicotine dependence.Significant association of the neurexin-1 gene (NRXN1) with nicotine dependence in European- and African-American smokersGenome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15Detection of genetic association and a functional polymorphism of dynamin 1 gene with nicotine dependence in European and African AmericansAssociation and interaction analyses of GABBR1 and GABBR2 with nicotine dependence in European- and African-American populations.Beta-arrestins 1 and 2 are associated with nicotine dependence in European American smokers.Significant association of ANKK1 and detection of a functional polymorphism with nicotine dependence in an African-American sample.Significant association of glutamate receptor, ionotropic N-methyl-D-aspartate 3A (GRIN3A), with nicotine dependence in European- and African-American smokersReplication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokers.Lack of association between genetic variation in G-protein-coupled receptor for asthma susceptibility and childhood asthma and atopyReview and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesA genome-wide scanning and fine mapping study of COGA dataComparison of genotype- and haplotype-based approaches for fine-mapping of alcohol dependence using COGA data.Accurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.
P2860
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P2860
Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics.
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Family-based tests for associa ...... pplication to asthma genetics.
@ast
Family-based tests for associa ...... pplication to asthma genetics.
@en
type
label
Family-based tests for associa ...... pplication to asthma genetics.
@ast
Family-based tests for associa ...... pplication to asthma genetics.
@en
prefLabel
Family-based tests for associa ...... pplication to asthma genetics.
@ast
Family-based tests for associa ...... pplication to asthma genetics.
@en
P2093
P356
P1433
P1476
Family-based tests for associa ...... pplication to asthma genetics.
@en
P2093
Edwin K Silverman
Scott T Weiss
Stephen L Lake
Steve Horvath
P356
10.1002/GEPI.10295
P577
2004-01-01T00:00:00Z