Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus.
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Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autismAssociation of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetesMultiple ADH genes modulate risk for drug dependence in both African- and European-AmericansAnalysis of sequence variability in the CART gene in relation to obesity in a Caucasian populationInterval estimation of genetic susceptibility for retrospective case-control studiesAssociation studies for asthma and atopic diseases: a comprehensive review of the literatureMAOA haplotypes associated with thrombocyte-MAO activity.ADH4 gene variation is associated with alcohol dependence and drug dependence in European Americans: results from HWD tests and case-control association studiesA test for genetic association that incorporates information about deviation from Hardy-Weinberg proportions in casesA single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations.Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's diseaseNovel tests for marker-disease association using the Collaborative Study on the Genetics of Alcoholism data.Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data.Measuring gametic disequilibrium from multilocus data.Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.Identifying the susceptibility gene(s) in a set of trait-linked genes using genotype data.A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes.Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs.High resolution T association tests of complex diseases based on family data.Fitting Proportional Odds Model to Case-Control data with Incorporating Hardy-Weinberg Equilibrium.Genetic associations in preterm birth: a primer of marker selection, study design, and data analysis.Simulating association studies: a data-based resampling method for candidate regions or whole genome scans.Detecting susceptibility genes in case-control studies using set associationFine-mapping using the weighted average method for a case-control study.Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD).Screening and replication using the same data set: testing strategies for family-based studies in which all probands are affectedDeviations from hardy-weinberg equilibrium in parental and unaffected sibling genotype dataCommon variants of inflammatory cytokine genes are associated with risk of nephropathy in type 2 diabetes among Asian Indians.Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.Replication study for the association of rs391300 in SRR and rs17584499 in PTPRD with susceptibility to type 2 diabetes in a Japanese population.Antioxidant defense enzyme genes and asthma susceptibility: gender-specific effects and heterogeneity in gene-gene interactions between pathogenetic variants of the diseaseHaplotype-based identification of a microsomal transfer protein marker associated with the human lifespan.A genetic ensemble approach for gene-gene interaction identificationPhase uncertainty in case-control association studies.Association of the rs738409 polymorphism in PNPLA3 with liver damage and the development of nonalcoholic fatty liver disease.Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOEUse of diplotypes - matched haplotype pairs from homologous chromosomes - in gene-disease association studies.Association study of DTNBP1 with schizophrenia in a US sample.Replication study for the association between four Loci identified by a genome-wide association study on European American subjects with type 1 diabetes and susceptibility to diabetic nephropathy in Japanese subjects with type 2 diabetes.Lupus susceptibility genes on human chromosome 1.
P2860
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P2860
Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Detecting marker-disease assoc ...... equilibrium at a marker locus.
@en
Detecting marker-disease assoc ...... equilibrium at a marker locus.
@nl
type
label
Detecting marker-disease assoc ...... equilibrium at a marker locus.
@en
Detecting marker-disease assoc ...... equilibrium at a marker locus.
@nl
prefLabel
Detecting marker-disease assoc ...... equilibrium at a marker locus.
@en
Detecting marker-disease assoc ...... equilibrium at a marker locus.
@nl
P356
P1476
Detecting marker-disease assoc ...... equilibrium at a marker locus.
@en
P2093
P304
P356
10.1086/302114
P407
P50
P577
1998-11-01T00:00:00Z