Family-based tests of association in the presence of linkage.
about
Genes to diseases (G2D) computational method to identify asthma candidate genesGenetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibilityReplication of association between working memory and Reelin, a potential modifier gene in schizophreniaGAD2 on chromosome 10p12 is a candidate gene for human obesityThe hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approachFamily-based association study of DYX1C1 variants in autismPowerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in malesFrom genomics to proteomics: new directions in molecular neuropsychiatry.A generalized family-based association test for dichotomous traits.Comparison of methods to account for relatedness in genome-wide association studies with family-based data.A genome-wide linkage and association study using COGA data.Comparison of genotype- and haplotype-based approaches for fine-mapping of alcohol dependence using COGA data.Identifying genetic variation affecting a complex trait in simulated data: a comparison of meta-analysis with pooled data analysis.An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.Joint modeling of linkage and association using affected sib-pair data.COGA phenotypes and linkages on chromosome 2.Surrogate phenotype definition for alcohol use disorders: a genome-wide search for linkage and association.Application of family-based association testing to assess the genotype-phenotype association involved in complex traits using single-nucleotide polymorphisms.Analysis of binary traits: testing association in the presence of linkage.Comparing strategies for association mapping in samples with related individuals.Hemoglobin binding to A beta and HBG2 SNP association suggest a role in Alzheimer's diseaseAssociation of killer cell immunoglobulin-like receptor genes with Hodgkin's lymphoma in a familial study.Empirically derived subgroups in rheumatoid arthritis: association with single-nucleotide polymorphisms on chromosome 6.Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche.Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritisUnivariate/multivariate genome-wide association scans using data from families and unrelated samples.Comparison of a unified analysis approach for family and unrelated samples with the transmission-disequilibrium test to study associations of hypertension in the Framingham Heart Study.An evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease: the GRACE-IMMUNE studyIdentification of two common variants contributing to serum apolipoprotein B levels in Mexicans.Genome wide linkage study, using a 250K SNP map, of Plasmodium falciparum infection and mild malaria attack in a Senegalese population.ROADTRIPS: case-control association testing with partially or completely unknown population and pedigree structure.A flexible model for association analysis in sibships with missing genotype data.Accounting for linkage in family-based tests of association with missing parental genotypesA common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in men.Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12Alleles of the NRAMP1 gene are risk factors for pediatric tuberculosis disease.The three-way relationship of polymorphisms of porcine genes encoding terminal complement components, their differential expression, and health-related phenotypesIntra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2.Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder.
P2860
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P2860
Family-based tests of association in the presence of linkage.
description
2000 nî lūn-bûn
@nan
2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Family-based tests of association in the presence of linkage.
@ast
Family-based tests of association in the presence of linkage.
@en
Family-based tests of association in the presence of linkage.
@nl
type
label
Family-based tests of association in the presence of linkage.
@ast
Family-based tests of association in the presence of linkage.
@en
Family-based tests of association in the presence of linkage.
@nl
prefLabel
Family-based tests of association in the presence of linkage.
@ast
Family-based tests of association in the presence of linkage.
@en
Family-based tests of association in the presence of linkage.
@nl
P2093
P2860
P356
P1476
Family-based tests of association in the presence of linkage.
@en
P2093
P2860
P304
P356
10.1086/316895
P407
P577
2000-10-31T00:00:00Z