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Cox, Nancy Jean
One or more keywords matched the following items that are connected to
Cox, Nancy Jean
Item Type
Name
Concept
Infant, Newborn
Concept
Heart Failure
Concept
Respiratory Distress Syndrome, Newborn
Concept
High-Throughput Screening Assays
Concept
Treatment Failure
Concept
Hearing Loss
Concept
Infant, Newborn, Diseases
Academic Article
Genetic aspects of early childhood stuttering.
Academic Article
Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
Academic Article
Genome-wide screen for atopy susceptibility alleles in the Hutterites.
Academic Article
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus.
Academic Article
Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.
Academic Article
A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.
Academic Article
Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.
Academic Article
Insulin gene mutations as a cause of permanent neonatal diabetes.
Academic Article
Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.
Academic Article
Prolonged shedding of amantadine-resistant influenzae A viruses by immunodeficient patients: detection by polymerase chain reaction-restriction analysis.
Academic Article
Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from the International Association of Diabetes and Pregnancy Study Groups.
Academic Article
Amantadine-resistant influenza A in nursing homes. Identification of a resistant virus prior to drug use.
Academic Article
Influenza-associated deaths among children in the United States, 2003-2004.
Academic Article
The total influenza vaccine failure of 1947 revisited: major intrasubtypic antigenic change can explain failure of vaccine in a post-World War II epidemic.
Academic Article
The economic impact of pandemic influenza in the United States: priorities for intervention.
Academic Article
An influenza A (H1N1) virus, closely related to swine influenza virus, responsible for a fatal case of human influenza.
Academic Article
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
Academic Article
Challenges in interpreting the evidence for genetic predictors of ototoxicity.
Academic Article
Integrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patients.
Academic Article
Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
Academic Article
Estimating heritability and genetic correlations from large health datasets in the absence of genetic data.
Academic Article
DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.
Academic Article
Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.
Academic Article
Pharmacogenomics of cisplatin-induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy.
Academic Article
Association of Genetically Predicted Fibroblast Growth Factor-23 with Heart Failure: A Mendelian Randomization Study.
Academic Article
Comprehensive association analysis of speech recognition thresholds after cisplatin-based chemotherapy in survivors of adult-onset cancer.
Academic Article
APOL1 and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus.
Search Criteria
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Newborn
Hearing
Screen