The University of Chicago Header Logo

Search Result Details

This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to Cox, Nancy Jean
Item TypeName
Concept Phenotype
Academic Article Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.
Academic Article Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma.
Academic Article Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
Academic Article Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
Academic Article Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome.
Academic Article Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians.
Academic Article Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED.
Academic Article Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA).
Academic Article Human genetics: an expression of interest.
Academic Article The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
Academic Article Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS.
Academic Article Genetic bases of the temperature-sensitive phenotype of a master donor virus used in live attenuated influenza vaccines: A/Leningrad/134/17/57 (H2N2).
Academic Article Genome-wide meta-analysis for severe diabetic retinopathy.
Academic Article The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy.
Academic Article Segregation analysis of speech and language disorders.
Academic Article Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior.
Academic Article Parent-of-origin effects of the serotonin transporter gene associated with autism.
Academic Article Copy number polymorphisms and anticancer pharmacogenomics.
Academic Article Next generation analytic tools for large scale genetic epidemiology studies of complex diseases.
Academic Article Variants affecting exon skipping contribute to complex traits.
Academic Article Influenza A virus haemagglutinin polymorphism: pleiotropic antigenic variants of A/Shanghai/11/87 (H3N2) virus selected as high yield reassortants.
Academic Article Stuttering: a complex behavioral disorder for our times?
Academic Article Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred.
Academic Article A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.
Academic Article Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
Academic Article Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
Academic Article Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans.
Academic Article Can recovery from stuttering be considered a genetically milder subtype of stuttering?
Academic Article Localization of MODY3 to a 5-cM region of human chromosome 12.
Academic Article An exponential combination procedure for set-based association tests in sequencing studies.
Academic Article Comprehensive genetic analysis of cytarabine sensitivity in a cell-based model identifies polymorphisms associated with outcome in AML patients.
Academic Article Integrative genomics: quantifying significance of phenotype-genotype relationships from multiple sources of high-throughput data.
Academic Article Genome-wide interrogation of longitudinal FEV1 in children with asthma.
Academic Article Poly-omic prediction of complex traits: OmicKriging.
Academic Article Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity.
Academic Article Genome-wide association studies in pharmacogenomics: successes and lessons.
Academic Article Structural architecture of SNP effects on complex traits.
Academic Article Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait.
Academic Article Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Academic Article Quantitative allelic test--a fast test for very large association studies.
Academic Article Obesity-associated variants within FTO form long-range functional connections with IRX3.
Academic Article Integrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patients.
Academic Article Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder.
Academic Article A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13.
Academic Article A gene-based association method for mapping traits using reference transcriptome data.
Academic Article Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx.
Academic Article Pharmacogenomic variants have larger effect sizes than genetic variants associated with other dichotomous complex traits.
Academic Article Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines.
Academic Article Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.
Academic Article STAMS: STRING-assisted module search for genome wide association studies and application to autism.
Academic Article Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record.
Academic Article Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.
Academic Article Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.
Academic Article Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Academic Article Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.
Academic Article An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
Academic Article LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.
Academic Article De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.
Academic Article GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.
Academic Article Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences.
Academic Article Estimating heritability and genetic correlations from large health datasets in the absence of genetic data.
Academic Article A brief history of human disease genetics.
Academic Article Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies.
Academic Article Electronic health record phenotypes associated with genetically regulated expression of CFTR and application to cystic fibrosis.
Academic Article Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.
Academic Article PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.
Academic Article Alcohol and cigarette smoking consumption as genetic proxies for alcohol misuse and nicotine dependence.
Academic Article Fate or coincidence: do COPD and major depression share genetic risk factors?
Academic Article Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities.
Academic Article Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing.
Academic Article Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Academic Article Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
Academic Article Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
Academic Article Exploration of an alternative to body mass index to characterize the relationship between height and weight for prediction of metabolic phenotypes and cardiovascular outcomes.
Academic Article Improving the computation efficiency of polygenic risk score modeling: faster in Julia.
Academic Article Discerning asthma endotypes through comorbidity mapping.
Academic Article A phenome-wide comparative analysis of genetic discordance between obesity and type 2 diabetes.
Academic Article Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study.
Academic Article Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19.
Academic Article The high-dimensional space of human diseases built from diagnosis records and mapped to genetic loci.
Academic Article Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI.
Search Criteria
  • Phenotype