Pages that link to "Q52432442"
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The following pages link to A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. (Q52432442):
Displaying 50 items.
- Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder (Q22252418) (← links)
- Searching for genetic determinants in the new millennium (Q22337300) (← links)
- Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia (Q24531526) (← links)
- Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13. (Q24538735) (← links)
- Genetic variation in the 22q11 locus and susceptibility to schizophrenia (Q24543969) (← links)
- The transmission/disequilibrium test: history, subdivision, and admixture (Q24671110) (← links)
- CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD (Q24811235) (← links)
- Cystathionine beta-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children (Q25257376) (← links)
- Genetic linkage analysis in the age of whole-genome sequencing (Q27027718) (← links)
- Synaptosomal-associated protein 25 (SNAP-25) and attention deficit hyperactivity disorder (ADHD): evidence of linkage and association in the Irish population (Q28201930) (← links)
- Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism (Q28246363) (← links)
- A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents. (Q28768577) (← 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)
- A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data (Q30655764) (← links)
- Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data (Q30721849) (← links)
- Genetic association tests for family data with missing parental genotypes: a comparison (Q30804771) (← links)
- Testing genetic association with rare and common variants in family data (Q30841941) (← links)
- Analysis of genetic linkage data for Mendelian traits (Q30856799) (← links)
- Adaptive combination of P-values for family-based association testing with sequence data (Q30881935) (← links)
- Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples (Q31094385) (← links)
- Mapping quantitative trait loci from a single-tail sample of the phenotype distribution including survival data. (Q31139618) (← links)
- A Monte Carlo procedure for two-stage tests with correlated data (Q31440382) (← links)
- Prediction of liability to orofacial clefting using genetic and craniofacial data from parents (Q32062109) (← links)
- Genotype relative-risks and association tests for nuclear families with missing parental data (Q32142336) (← links)
- PRKCA and multiple sclerosis: association in two independent populations (Q33238942) (← links)
- Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls (Q33352742) (← links)
- Basic concepts in the study of diseases with complex genetics (Q33544009) (← links)
- Benefits and pitfalls encountered in psychiatric genetic association studies (Q33544011) (← links)
- Overview of techniques to account for confounding due to population stratification and cryptic relatedness in genomic data association analyses. (Q33632115) (← links)
- Haplotype association analyses in resources of mixed structure using Monte Carlo testing (Q33766979) (← links)
- Search for schizophrenia susceptibility genes (Q33842584) (← links)
- Accounting for Linkage in Family-Based Tests of Association with Missing Parental Genotypes (Q33905574) (← links)
- Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12 (Q33910053) (← links)
- Association testing in a linked region using large pedigrees (Q33938702) (← links)
- Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population (Q33938710) (← links)
- The genetics of Tourette syndrome (Q33940186) (← links)
- Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder (Q33943718) (← links)
- Gene mapping by linkage and association analysis (Q33996962) (← links)
- Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes (Q34020712) (← links)
- Linkage and association: basic concepts (Q34063979) (← links)
- Genotype-environment interaction in transmission disequilibrium tests (Q34064028) (← links)
- Optimum study designs (Q34064068) (← links)
- Genetics of familial combined hyperlipidemia (Q34107190) (← links)
- Multipoint linkage-disequilibrium-mapping approach based on the case-parent trio design (Q34114687) (← links)
- Dopamine D4 receptors modulate brain metabolic activity in the prefrontal cortex and cerebellum at rest and in response to methylphenidate (Q34121778) (← links)
- Molecular genetic and family studies in affective disorders: state of the art. (Q34137588) (← links)
- Statistical approaches to gene mapping (Q34142054) (← links)
- Transmission/disequilibrium tests using multiple tightly linked markers (Q34144172) (← links)