Pages that link to "Q35194809"

The following pages link to Genotype relative risks: methods for design and analysis of candidate-gene association studies (Q35194809):

Displaying 50 items.

• Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia (Q21091121) ‎ (← links)
• Heterogeneity and the genetics of autism (Q24535727) ‎ (← links)
• ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies (Q24812292) ‎ (← links)
• Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism (Q25257386) ‎ (← links)
• Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies (Q27330547) ‎ (← links)
• Review and evaluation of methods correcting for population stratification with a focus on underlying statistical principles (Q30492697) ‎ (← links)
• Detection of disease genes by use of family data. I. Likelihood-based theory (Q30588489) ‎ (← links)
• LRTae: improving statistical power for genetic association with case/control data when phenotype and/or genotype misclassification errors are present (Q30814821) ‎ (← links)
• Bootstrap calibration of TRANSMIT for informative missingness of parental genotype data (Q30907462) ‎ (← links)
• Precision 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 statistics (Q31031507) ‎ (← links)
• Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data (Q31151241) ‎ (← links)
• 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 (Q32074789) ‎ (← links)
• Genetic association analysis using data from triads and unrelated subjects (Q33211937) ‎ (← links)
• Identifying susceptibility genes by using joint tests of association and linkage and accounting for epistasis (Q33232741) ‎ (← links)
• Linkage and association analysis in pedigrees from different populations (Q33232806) ‎ (← links)
• Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes (Q33255336) ‎ (← links)
• Incorporation of genetic model parameters for cost-effective designs of genetic association studies using DNA pooling (Q33290992) ‎ (← links)
• Joint analysis of case-parents trio and unrelated case-control designs in large scale association studies (Q33332923) ‎ (← links)
• The genetics of preterm birth: using what we know to design better association studies (Q33566643) ‎ (← links)
• Sex chromosomes and genetic association studies (Q33600130) ‎ (← links)
• A weak association between TH and DRD2 genes and bipolar affective disorder in a Spanish sample (Q33675777) ‎ (← links)
• Family studies of type 1 diabetes reveal additive and epistatic effects between MGAT1 and three other polymorphisms (Q33717572) ‎ (← links)
• Haplotype association analyses in resources of mixed structure using Monte Carlo testing (Q33766979) ‎ (← links)
• Robust joint analysis allowing for model uncertainty in two-stage genetic association studies (Q33787548) ‎ (← links)
• Informative missingness in genetic association studies: case-parent designs (Q33904539) ‎ (← links)
• Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia (Q33960039) ‎ (← links)
• Utilizing population controls in rare-variant case-parent association tests (Q34000914) ‎ (← links)
• Caffeine, selected metabolic gene variants, and risk for neural tube defects (Q34051331) ‎ (← links)
• Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation (Q34093903) ‎ (← links)
• Family-based association tests using genotype data with uncertainty (Q34096126) ‎ (← links)
• A hybrid design for studying genetic influences on risk of diseases with onset early in life (Q34114547) ‎ (← links)
• TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data (Q34134550) ‎ (← links)
• The use of case-parent triads to study joint effects of genotype and exposure (Q34146147) ‎ (← links)
• Exploration and comparison of methods for combining population- and family-based genetic association using the Genetic Analysis Workshop 17 mini-exome (Q34176896) ‎ (← links)
• 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 controls (Q34384399) ‎ (← links)
• Transmission disequilibrium, family controls, and great expectations (Q34387553) ‎ (← links)
• Allowing for missing parents in genetic studies of case-parent triads (Q34389420) ‎ (← links)
• Methods for detection of parent-of-origin effects in genetic studies of case-parents triads (Q34390867) ‎ (← links)
• Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring (Q34511692) ‎ (← links)
• Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study (Q34868144) ‎ (← links)
• Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. (Q34959002) ‎ (← links)
• Association analysis of complex diseases using triads, parent-child dyads and singleton monads (Q34978919) ‎ (← links)
• Detecting rare variants in case-parents association studies (Q35004969) ‎ (← links)
• Correction for multiplicity in genetic association studies of triads: the permutational TDT (Q35051439) ‎ (← links)
• Family-based gene-by-environment interaction studies: revelations and remedies (Q35095104) ‎ (← links)
• Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants (Q35616533) ‎ (← links)
• A generalized sequential Bonferroni procedure using smoothed weights for genome-wide association studies incorporating information on Hardy-Weinberg disequilibrium among cases. (Q35709443) ‎ (← links)
• Comparison of statistics for candidate-gene association studies using cases and parents (Q35889597) ‎ (← links)
• Identification of risk-related haplotypes with the use of multiple SNPs from nuclear families (Q35946571) ‎ (← links)
• Genetic association studies of complex neurological diseases (Q36142031) ‎ (← links)