Efficient study designs for test of genetic association using sibship data and unrelated cases and controls.
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CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degenerationProceedings: consideration of genetics in the design of induced pluripotent stem cell-based models of complex diseaseExome sequencing and complex disease: practical aspects of rare variant association studiesGenome-wide linkage on chromosome 10q26 for a dimensional scale of major depressionCntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmissionGenome-wide association study of the rate of cognitive decline in Alzheimer's disease.SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians.An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.Linkage and association analysis of GAW15 simulated data: fine-mapping of chromosome 6 region.An integrated genome-wide association analysis on rheumatoid arthritis data.Joint linkage and association analysis for identification of potentially causal polymorphisms in GAW15 data.Genetic and functional association of FAM5C with myocardial infarctionTwo-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategiesGenome-wide linkage and association analysis of rheumatoid arthritis in a Canadian populationA new score statistic to test for association given linkage in affected sibling pair-control designs.Identifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association.Replication of association between ADAM33 polymorphisms and psoriasis.Haplotype association analysis of combining unrelated case-control and triads with consideration of population stratification.Three ways of combining genotyping and resequencing in case-control association studies.A flexible model for association analysis in sibships with missing genotype data.Assessing the contribution family data can make to case-control studies of rare variants.Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locusA unified framework for detecting rare variant quantitative trait associations in pedigree and unrelated individuals via sequence data.Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.Validity and power of association testing in family-based sampling designs: evidence for and against the common wisdom.Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel lociAssociation analysis of complex diseases using triads, parent-child dyads and singleton monads.Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals.A single-nucleotide polymorphism in the EAP1 gene is associated with amenorrhea/oligomenorrhea in nonhuman primates.On the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case-control samples.Identification and validation of risk loci for osteochondrosis in standardbreds.Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models.A novel locus on chromosome 1 underlies the evolution of a melanic plumage polymorphism in a wild songbirdPedGenie: meta genetic association testing in mixed family and case-control designs.Family-based association tests for genomewide association scans.
P2860
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P2860
Efficient study designs for test of genetic association using sibship data and unrelated cases and controls.
description
2006 nî lūn-bûn
@nan
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Efficient study designs for te ...... unrelated cases and controls.
@ast
Efficient study designs for te ...... unrelated cases and controls.
@en
Efficient study designs for te ...... unrelated cases and controls.
@en-gb
type
label
Efficient study designs for te ...... unrelated cases and controls.
@ast
Efficient study designs for te ...... unrelated cases and controls.
@en
Efficient study designs for te ...... unrelated cases and controls.
@en-gb
prefLabel
Efficient study designs for te ...... unrelated cases and controls.
@ast
Efficient study designs for te ...... unrelated cases and controls.
@en
Efficient study designs for te ...... unrelated cases and controls.
@en-gb
P2860
P356
P1476
Efficient study designs for te ...... unrelated cases and controls.
@en
P2093
Mingyao Li
P2860
P304
P356
10.1086/503711
P407
P577
2006-03-20T00:00:00Z