Genotype relative risks: methods for design and analysis of candidate-gene association studies.
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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from ScandinaviaHeterogeneity and the genetics of autism.ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies.Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autismUsing ancestry matching to combine family-based and unrelated samples for genome-wide association studiesReview and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesDetection of disease genes by use of family data. I. Likelihood-based theoryLRTae: improving statistical power for genetic association with case/control data when phenotype and/or genotype misclassification errors are presentBootstrap calibration of TRANSMIT for informative missingness of parental genotype dataPrecision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae statisticsLikelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.Genetic association analysis using data from triads and unrelated subjectsIdentifying susceptibility genes by using joint tests of association and linkage and accounting for epistasis.Linkage and association analysis in pedigrees from different populationsAre molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes.Incorporation of genetic model parameters for cost-effective designs of genetic association studies using DNA pooling.Joint analysis of case-parents trio and unrelated case-control designs in large scale association studiesThe genetics of preterm birth: using what we know to design better association studiesSex chromosomes and genetic association studies.A weak association between TH and DRD2 genes and bipolar affective disorder in a Spanish sampleFamily studies of type 1 diabetes reveal additive and epistatic effects between MGAT1 and three other polymorphismsHaplotype association analyses in resources of mixed structure using Monte Carlo testingRobust joint analysis allowing for model uncertainty in two-stage genetic association studiesInformative missingness in genetic association studies: case-parent designs.Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemiaUtilizing population controls in rare-variant case-parent association testsCaffeine, selected metabolic gene variants, and risk for neural tube defects.Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation.Family-based association tests using genotype data with uncertainty.A hybrid design for studying genetic influences on risk of diseases with onset early in lifeTDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.The use of case-parent triads to study joint effects of genotype and exposure.Exploration and comparison of methods for combining population- and family-based genetic association using the Genetic Analysis Workshop 17 mini-exome.Susceptibility to relapsing-progressive multiple sclerosis is associated with inheritance of genes linked to the variable region of the TcR beta locus: use of affected family-based controlsTransmission disequilibrium, family controls, and great expectationsAllowing for missing parents in genetic studies of case-parent triadsMethods for detection of parent-of-origin effects in genetic studies of case-parents triads.Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring.Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study
P2860
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P2860
Genotype relative risks: methods for design and analysis of candidate-gene association studies.
description
1993 nî lūn-bûn
@nan
1993 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Genotype relative risks: metho ...... date-gene association studies.
@ast
Genotype relative risks: metho ...... date-gene association studies.
@en
type
label
Genotype relative risks: metho ...... date-gene association studies.
@ast
Genotype relative risks: metho ...... date-gene association studies.
@en
prefLabel
Genotype relative risks: metho ...... date-gene association studies.
@ast
Genotype relative risks: metho ...... date-gene association studies.
@en
P2860
P1476
Genotype relative risks: metho ...... date-gene association studies.
@en
P2093
D J Schaid
S S Sommer
P2860
P304
P407
P577
1993-11-01T00:00:00Z