Pages that link to "Q34398834"

The following pages link to Using linkage genome scans to improve power of association in genome scans (Q34398834):

Displaying 50 items.

• Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study (Q21092472) ‎ (← links)
• Learning a prior on regulatory potential from eQTL data (Q21145013) ‎ (← links)
• Finding the missing heritability of complex diseases (Q22122198) ‎ (← links)
• Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response (Q24289192) ‎ (← links)
• A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder (Q24655759) ‎ (← links)
• Comprehensive testing of positionally cloned asthma genes in two populations (Q24670496) ‎ (← links)
• The role of large pedigrees in an era of high-throughput sequencing (Q26825546) ‎ (← links)
• Two-phase and family-based designs for next-generation sequencing studies (Q26828744) ‎ (← links)
• A new methodology to associate SNPs with human diseases according to their pathway related context (Q28477617) ‎ (← links)
• Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis (Q28740719) ‎ (← links)
• Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms (Q28752178) ‎ (← links)
• Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians (Q28943474) ‎ (← links)
• Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. (Q28943477) ‎ (← links)
• Replicating genotype-phenotype associations (Q29614919) ‎ (← links)
• Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis (Q30426239) ‎ (← links)
• Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia (Q30439012) ‎ (← links)
• Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates (Q30490128) ‎ (← links)
• Pathway-based analysis using genome-wide association data from a Korean non-small cell lung cancer study (Q30647266) ‎ (← links)
• Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data (Q30879682) ‎ (← links)
• Powerful association test combining rare variant and gene expression using family data from Genetic Analysis Workshop 19. (Q31149258) ‎ (← links)
• The multiplicity problem in linkage analysis of gene expression data - the power of differentiating cis- and trans-acting regulators (Q31154850) ‎ (← links)
• A pragmatic suggestion for dealing with results for candidate genes obtained from genome wide association studies (Q33284162) ‎ (← links)
• A high-density admixture scan in 1,670 African Americans with hypertension (Q33306108) ‎ (← links)
• A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples (Q33314661) ‎ (← links)
• Genetic loci linked to type 1 diabetes and multiple sclerosis families in Sardinia (Q33315480) ‎ (← links)
• Joint study of genetic regulators for expression traits related to breast cancer (Q33332757) ‎ (← links)
• Genome-wide association analyses of North American Rheumatoid Arthritis Consortium and Framingham Heart Study data utilizing genome-wide linkage results (Q33519208) ‎ (← links)
• Comparison of univariate and multivariate linkage analysis of traits related to hypertension (Q33519420) ‎ (← links)
• Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration (Q33533937) ‎ (← links)
• Poor replication of candidate genes for major depressive disorder using genome-wide association data (Q33547331) ‎ (← links)
• Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS). (Q33570929) ‎ (← links)
• A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease (Q33596843) ‎ (← links)
• Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies (Q33612076) ‎ (← links)
• Incorporation of covariates in simultaneous localization of two linked loci using affected relative pairs (Q33631773) ‎ (← links)
• High-Density Genomewide Linkage Analysis of Exceptional Human Longevity Identifies Multiple Novel Loci (Q33687271) ‎ (← links)
• Refined QTLs of osteoporosis-related traits by linkage analysis with genome-wide SNPs: Framingham SHARe (Q33742242) ‎ (← links)
• Improved detection of rare genetic variants for diseases (Q33747787) ‎ (← links)
• Multi-locus Test Conditional on Confirmed Effects Leads to Increased Power in Genome-wide Association Studies (Q33754653) ‎ (← links)
• Predicting functionally important SNP classes based on negative selection (Q33797313) ‎ (← links)
• Prioritized subset analysis: improving power in genome-wide association studies (Q33805649) ‎ (← links)
• Genetic susceptibility in Juvenile Myoclonic Epilepsy: Systematic review of genetic association studies. (Q33821815) ‎ (← links)
• Using linkage information to weight a genome-wide association of bipolar disorder (Q33867868) ‎ (← links)
• Gene-environment interaction and children's health and development (Q33885540) ‎ (← links)
• SPOT: a web-based tool for using biological databases to prioritize SNPs after a genome-wide association study (Q33957829) ‎ (← links)
• Combining information from linkage and association methods (Q34022088) ‎ (← links)
• Bayesian mixture models for the incorporation of prior knowledge to inform genetic association studies (Q34022116) ‎ (← links)
• INSIG2 SNPs associated with obesity and glucose homeostasis traits in Hispanics: the IRAS Family Study (Q34046787) ‎ (← links)
• Genome-Wide Significance Levels and Weighted Hypothesis Testing (Q34061938) ‎ (← links)
• Analysis of genome-wide association study data using the protein knowledge base (Q34072996) ‎ (← links)
• Identification of rare variants for hypertension with incorporation of linkage information (Q34088674) ‎ (← links)