sameAs
Chapter 11: Genome-wide association studiesLearning Classifier Systems: A Complete Introduction, Review, and RoadmapThe genetic structure and history of Africans and African AmericansDiverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factorsA high-density admixture map for disease gene discovery in african americansA gene expression fingerprint of C. elegans embryonic motor neuronsOptimization of neural network architecture using genetic programming improves detection and modeling of gene-gene interactions in studies of human diseasesAn application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene interactions on risk of myocardial infarction: the importance of model validationSystems genetics for drug target discoveryEffect of genetic variants, especially CYP2C9 and VKORC1, on the pharmacology of warfarinA flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibilityAdmixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody productionGenetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkersThe golden era of biomedical informatics has begunThe future of genomic medicine education in AfricaGenome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.Evolving hard problems: Generating human genetics datasets with a complex etiologyMissing heritability and strategies for finding the underlying causes of complex diseaseGenetic Effects on the Correlation Structure of CVD Risk Factors: Exome-Wide Data From a Ghanaian Population.Embracing Complex Associations in Common Traits: Critical Considerations for Precision Medicine.Differential Response to High Glucose in Skin Fibroblasts of Monozygotic Twins Discordant for Type 1 DiabetesDifferential Gene Expression in Diabetic Nephropathy in Individuals With Type 1 Diabetes.Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulationA meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.Gene expression differences in skin fibroblasts in identical twins discordant for type 1 diabetes.Genetic population structure analysis in New Hampshire reveals Eastern European ancestryIon channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing.Computational genetics analysis of grey matter density in Alzheimer's disease.Accelerating epistasis analysis in human genetics with consumer graphics hardwareMultifactor dimensionality reduction for graphics processing units enables genome-wide testing of epistasis in sporadic ALS.Exploiting graphics processing units for computational biology and bioinformatics.Detection of linear and nonlinear dependencies in time series using the method of surrogate data in S-PLUS.The limits of p-values for biological data miningThe disconnect between classical biostatistics and the biological data mining community.The central role of biological data mining in connecting diverse disciplinesSymbolic discriminant analysis of microarray data in autoimmune disease.Big Data analysis on autopilot?Big data bioinformatics.The critical need for computational methods and software for simulating complex genetic and genomic data.
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