Pages that link to "Q35889597"
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The following pages link to Comparison of statistics for candidate-gene association studies using cases and parents (Q35889597):
Displaying 37 items.
- The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. (Q24540193) (← links)
- The transmission/disequilibrium test: history, subdivision, and admixture (Q24671110) (← links)
- The TDT and other family-based tests for linkage disequilibrium and association (Q24675685) (← links)
- Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies (Q27330547) (← links)
- Evaluating diagnostic accuracy of genetic profiles in affected offspring families (Q28383346) (← links)
- Genetic analysis of type 1 diabetes using whole genome approaches (Q28776047) (← links)
- Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism (Q28943360) (← 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)
- Detection of disease genes by use of family data. II. Application to nuclear families (Q30588493) (← links)
- Genetic association analysis using data from triads and unrelated subjects (Q33211937) (← links)
- Impact of non-ignorable missingness on genetic tests of linkage and/or association using case-parent trios. (Q33232846) (← links)
- Linkage of rheumatoid arthritis to the candidate gene NRAMP1 on 2q35 (Q33677668) (← links)
- Candidate-gene association studies of schizophrenia (Q33707751) (← links)
- Genetics of bipolar disorder. (Q33721526) (← links)
- Melanocortin-4 receptor gene variant I103 is negatively associated with obesity (Q33930734) (← links)
- Comparison of tests for association and linkage in incomplete families (Q34141800) (← links)
- Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions (Q34145152) (← links)
- Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects (Q34146787) (← links)
- Analytical methods for disease association studies with immunogenetic data (Q34291937) (← links)
- Mapping of complex traits by single-nucleotide polymorphisms (Q34386114) (← links)
- Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity (Q34388239) (← links)
- Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition (Q34389371) (← links)
- Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies (Q34389628) (← links)
- Learning about the X from our parents (Q35067109) (← links)
- Power studies for the transmission/disequilibrium tests with multiple alleles (Q35238800) (← links)
- A paradigm for finding genes for a complex human trait: polycystic ovary syndrome and follistatin (Q35992640) (← links)
- Empirical pathway analysis, without permutation (Q36916419) (← links)
- Joint genetic susceptibility to type 1 diabetes and autoimmune thyroiditis: from epidemiology to mechanisms. (Q36973929) (← links)
- Genetic epidemiology of infectious diseases in humans: design of population-based studies (Q37092587) (← links)
- Allowing for population stratification in case-only studies of gene-environment interaction, using genomic control (Q40617466) (← links)
- The role of candidate genes in the etiology of schizophrenia (Q41278323) (← links)
- Linkage and association of the HLA gene complex with IDDM in 81 Danish families: strong linkage between DR beta 1Lys71+ and IDDM (Q42284419) (← links)
- Evidence of linkage disequilibrium between schizophrenia and the SCa1 CAG repeat on chromosome 6p23 (Q42588936) (← links)
- Genetics and pulmonary medicine. 3. Genetic susceptibility to tuberculosis in human populations (Q43061105) (← links)
- Allelic heterogeneity in genetic association meta-analysis: an application to DTNBP1 and schizophrenia (Q44952517) (← links)
- Detecting non-multiplicative genotype relative risks from transmissions of parental alleles to affected children (Q81146220) (← links)