Pages that link to "Q88032932"
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The following pages link to Eric E Schadt (Q88032932):
Displaying 50 items.
- Multi-tissue coexpression networks reveal unexpected subnetworks associated with disease (Q21183892) (← links)
- Optimization of oligonucleotide arrays and RNA amplification protocols for analysis of transcript structure and alternative splicing (Q21194880) (← links)
- Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies (Q21283815) (← links)
- Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease (Q22251082) (← links)
- Genetic studies of body mass index yield new insights for obesity biology (Q22305005) (← links)
- The arrestin domain-containing 3 protein regulates body mass and energy expenditure (Q24339493) (← links)
- Modeling kinetic rate variation in third generation DNA sequencing data to detect putative modifications to DNA bases (Q24596678) (← links)
- Common variants at 30 loci contribute to polygenic dyslipidemia (Q24598765) (← links)
- Variations in DNA elucidate molecular networks that cause disease (Q24622333) (← links)
- Biological, clinical and population relevance of 95 loci for blood lipids (Q24622541) (← links)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (Q24630979) (← links)
- From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus (Q24633183) (← links)
- A comprehensive transcript index of the human genome generated using microarrays and computational approaches (Q24809389) (← links)
- Genomic analysis of metabolic pathway gene expression in mice (Q24812680) (← links)
- Genetic and genomic analysis of a fat mass trait with complex inheritance reveals marked sex specificity (Q25257837) (← links)
- Extensive sequencing of seven human genomes to characterize benchmark reference materials (Q27309266) (← links)
- iPSC-derived dopamine neurons reveal differences between monozygotic twins discordant for Parkinson's disease (Q27321433) (← links)
- Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project (Q27324648) (← links)
- Prediction of Causal Candidate Genes in Coronary Artery Disease Loci (Q27342192) (← links)
- Validation of ITD mutations in FLT3 as a therapeutic target in human acute myeloid leukaemia (Q27851767) (← links)
- Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders (Q28082561) (← links)
- Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays (Q28235146) (← links)
- Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany (Q28244221) (← links)
- Dosage compensation is less effective in birds than in mammals (Q28292598) (← links)
- The origin of the Haitian cholera outbreak strain (Q28300132) (← links)
- Meta-analysis of inter-species liver co-expression networks elucidates traits associated with common human diseases (Q28472207) (← links)
- Mapping the genetic architecture of gene expression in human liver (Q28472693) (← links)
- Characterizing dynamic changes in the human blood transcriptional network (Q28472852) (← links)
- Bayesian test for colocalisation between pairs of genetic association studies using summary statistics (Q28660129) (← links)
- Leveraging models of cell regulation and GWAS data in integrative network-based association studies (Q28704307) (← links)
- Dissecting cis regulation of gene expression in human metabolic tissues (Q28740835) (← links)
- Disentangling molecular relationships with a causal inference test (Q28742231) (← links)
- Predictive genes in adjacent normal tissue are preferentially altered by sCNV during tumorigenesis in liver cancer and may rate limiting (Q28742950) (← links)
- Identification of genes and networks driving cardiovascular and metabolic phenotypes in a mouse F2 intercross (Q28744247) (← links)
- The quantitative genetics of phenotypic robustness (Q28749448) (← links)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (Q28943288) (← links)
- Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (Q29417023) (← links)
- Common body mass index-associated variants confer risk of extreme obesity (Q29417063) (← links)
- Genetics of gene expression and its effect on disease (Q29614591) (← links)
- Genomic profiling reveals mutational landscape in parathyroid carcinomas (Q30360213) (← links)
- A Cytosine Methyltransferase Modulates the Cell Envelope Stress Response in the Cholera Pathogen [corrected]. (Q30397967) (← links)
- Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis (Q30411394) (← links)
- Loss of CDKN2B promotes p53-dependent smooth muscle cell apoptosis and aneurysm formation (Q30415442) (← links)
- A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry (Q30416161) (← links)
- Genome scans for transmission ratio distortion regions in mice (Q30419551) (← links)
- CR1 and the "vanishing amyloid" hypothesis of Alzheimer's disease (Q30421877) (← links)
- Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (Q30425020) (← links)
- An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits (Q30435869) (← links)
- An integrative genetics approach to identify candidate genes regulating BMD: combining linkage, gene expression, and association (Q30437488) (← links)
- Genome-wide mapping of methylated adenine residues in pathogenic Escherichia coli using single-molecule real-time sequencing (Q30444920) (← links)