Item Type | Name |
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
|
Gene-gene interaction in asthma: IL4RA and IL13 in a Dutch population with asthma.
|
Academic Article
|
Genome-wide search for atopy susceptibility genes in Dutch families with asthma.
|
Academic Article
|
Common estrogen receptor polymorphism augments effects of hormone replacement therapy on E-selectin but not C-reactive protein.
|
Academic Article
|
Factor V Leiden, hormone replacement therapy, and risk of venous thromboembolic events in women with coronary disease.
|
Academic Article
|
Mapping susceptibility genes for allergic diseases.
|
Academic Article
|
ER-alpha variants and the cardiovascular effects of hormone replacement therapy.
|
Academic Article
|
Spontaneous regression of advanced cancer: identification of a unique genetically determined, age-dependent trait in mice.
|
Academic Article
|
CLC-2 single nucleotide polymorphisms (SNPs) as potential modifiers of cystic fibrosis disease severity.
|
Academic Article
|
Genome screen for asthma and bronchial hyperresponsiveness: interactions with passive smoke exposure.
|
Academic Article
|
Effect of genetic variations in platelet glycoproteins Ibalpha and VI on the risk for coronary heart disease events in postmenopausal women taking hormone therapy.
|
Academic Article
|
Common beta-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease.
|
Academic Article
|
Association of polymorphisms in genes involved in lipoprotein metabolism with plasma concentrations of remnant lipoproteins and HDL subpopulations before and after hormone therapy in postmenopausal women.
|
Academic Article
|
Comparative analyses of single-nucleotide polymorphisms in the TNF promoter region provide further validation for the vervet monkey model of obesity.
|
Academic Article
|
Single-nucleotide polymorphisms in the TNF gene are associated with obesity-related phenotypes in vervet monkeys.
|
Academic Article
|
Importance of hedgehog interacting protein and other lung function genes in asthma.
|
Academic Article
|
Common variants in the periostin gene influence development of atherosclerosis in young persons.
|
Academic Article
|
Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.
|
Academic Article
|
Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.
|
Academic Article
|
Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis.
|
Academic Article
|
D20S16 is a complex interspersed repeated sequence: genetic and physical analysis of the locus.
|
Academic Article
|
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy.
|
Academic Article
|
Association of autoimmune thyroid disease with a microsatellite marker for the thyrotropin receptor gene and CTLA-4 in a Japanese population.
|
Academic Article
|
Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus.
|
Academic Article
|
Genetics of allergy and bronchial hyperresponsiveness.
|
Academic Article
|
Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
|
Academic Article
|
Major genes regulating total serum immunoglobulin E levels in families with asthma.
|
Academic Article
|
Association of a promoter polymorphism of the CD14 gene and atopy.
|
Academic Article
|
Identification and association of polymorphisms in the interleukin-13 gene with asthma and atopy in a Dutch population.
|
Academic Article
|
Estrogen-receptor polymorphisms and effects of estrogen replacement on high-density lipoprotein cholesterol in women with coronary disease.
|
Academic Article
|
Major recessive gene(s) with considerable residual polygenic effect regulating adult height: confirmation of genomewide scan results for chromosomes 6, 9, and 12.
|
Academic Article
|
Fine mapping of an IgE-controlling gene on chromosome 2q: Analysis of CTLA4 and CD28.
|
Academic Article
|
Association of a disintegrin and metalloprotease 33 (ADAM33) gene with asthma in ethnically diverse populations.
|
Academic Article
|
Polymorphisms of the ADAM33 gene are associated with accelerated lung function decline in asthma.
|
Academic Article
|
Identification of polymorphisms in the human glucocorticoid receptor gene (NR3C1) in a multi-racial asthma case and control screening panel.
|
Academic Article
|
Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
|
Academic Article
|
Genomewide screen for pulmonary function in 200 families ascertained for asthma.
|
Academic Article
|
Promoter polymorphisms in the nitric oxide synthase 3 gene are associated with ischemic stroke susceptibility in young black women.
|
Academic Article
|
Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
|
Academic Article
|
Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes.
|
Academic Article
|
Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study.
|
Academic Article
|
Identification of PCDH1 as a novel susceptibility gene for bronchial hyperresponsiveness.
|
Academic Article
|
Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.
|
Academic Article
|
Interleukin 13 and interleukin 4 receptor-a polymorphisms in rhinitis and asthma.
|
Academic Article
|
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.
|
Academic Article
|
Epigenetic changes with dietary soy in cynomolgus monkeys.
|
Academic Article
|
Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium.
|
Academic Article
|
Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome.
|
Academic Article
|
D20S213, a microsatellite polymorphism near the D20S16 locus.
|
Academic Article
|
Physical and genetic mapping of the muscle phosphofructokinase gene (PFKM): reassignment to human chromosome 12q.
|
Academic Article
|
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.
|
Academic Article
|
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.
|
Academic Article
|
Fluorescent allele-specific PCR (FAS-PCR) improves the reliability of single nucleotide polymorphism screening.
|
Academic Article
|
A physical map of the 20q12-q13.1 region associated with type 2 diabetes.
|
Academic Article
|
Mapping susceptibility genes for asthma and allergy.
|
Concept
|
Body Weights and Measures
|
Concept
|
Electrophoresis, Polyacrylamide Gel
|
Concept
|
Respiratory Function Tests
|
Concept
|
Longitudinal Studies
|
Concept
|
Physical Chromosome Mapping
|
Concept
|
Psychiatric Status Rating Scales
|
Concept
|
Epigenesis, Genetic
|
Concept
|
Contig Mapping
|
Concept
|
Models, Genetic
|
Concept
|
Sequence Alignment
|
Concept
|
Polymorphism, Genetic
|
Concept
|
Research Design
|
Concept
|
Genetic Testing
|
Concept
|
Interviews as Topic
|
Concept
|
Demography
|
Concept
|
Family
|
Concept
|
Random Allocation
|
Concept
|
Cohort Studies
|
Concept
|
Databases, Genetic
|
Concept
|
Skin Tests
|
Concept
|
Radiography
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Genetic Loci
|
Concept
|
Logistic Models
|
Concept
|
Genetic Techniques
|
Concept
|
Genetic Markers
|
Concept
|
Clinical Trials as Topic
|
Concept
|
Genetic Variation
|
Concept
|
Estrogen Replacement Therapy
|
Concept
|
Transcription, Genetic
|
Concept
|
Chromatography, High Pressure Liquid
|
Concept
|
Hormone Replacement Therapy
|
Concept
|
Ovariectomy
|
Concept
|
Mutagenesis, Insertional
|
Concept
|
Paraffin Embedding
|
Concept
|
Multicenter Studies as Topic
|
Concept
|
Genetic Heterogeneity
|
Concept
|
DNA Mutational Analysis
|
Concept
|
Microscopy, Electron, Scanning
|
Concept
|
Gene Expression Profiling
|
Concept
|
Tandem Mass Spectrometry
|
Concept
|
Blotting, Southern
|
Concept
|
Nutrition Surveys
|
Concept
|
Genetic Load
|
Concept
|
Sequence Analysis, DNA
|
Concept
|
Patient Selection
|
Concept
|
Bronchial Provocation Tests
|
Concept
|
Genetic Association Studies
|
Concept
|
Restriction Mapping
|
Concept
|
Tissue Fixation
|
Concept
|
Flow Cytometry
|
Concept
|
Epistasis, Genetic
|
Concept
|
Magnetic Resonance Imaging
|
Concept
|
Drug Therapy, Combination
|
Concept
|
Case-Control Studies
|
Concept
|
Crosses, Genetic
|
Concept
|
Prospective Studies
|
Concept
|
Cross-Sectional Studies
|
Concept
|
Chromosome Mapping
|
Concept
|
Randomized Controlled Trials as Topic
|
Concept
|
Genome-Wide Association Study
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
Concept
|
Transfection
|
Concept
|
Polymerase Chain Reaction
|
Concept
|
Neuropsychological Tests
|
Concept
|
Risk Assessment
|
Concept
|
In Situ Hybridization, Fluorescence
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Whole-Body Irradiation
|
Concept
|
Recombination, Genetic
|
Concept
|
Follow-Up Studies
|
Concept
|
Autopsy
|
Concept
|
Community-Based Participatory Research
|
Concept
|
Immunohistochemistry
|
Concept
|
Protein Array Analysis
|
Concept
|
Electrocardiography
|
Academic Article
|
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
|
Academic Article
|
Influence of sex and diet on quantitative trait loci for HDL cholesterol levels in an SM/J by NZB/BlNJ intercross population.
|
Academic Article
|
Methylomics of gene expression in human monocytes.
|
Academic Article
|
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
|
Academic Article
|
The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome.
|
Academic Article
|
DNA Methylation of the Aryl Hydrocarbon Receptor Repressor Associations With Cigarette Smoking and Subclinical Atherosclerosis.
|
Academic Article
|
Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
|
Academic Article
|
Germline BAP1 Mutational Landscape of Asbestos-Exposed Malignant Mesothelioma Patients with Family History of Cancer.
|
Academic Article
|
Impact of Genetic and Epigenetic Variations Within the FADS Cluster on the Composition and Metabolism of Polyunsaturated Fatty Acids in Prostate Cancer.
|
Academic Article
|
Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci.
|
Academic Article
|
Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.
|
Academic Article
|
Transancestral mapping and genetic load in systemic lupus erythematosus.
|
Academic Article
|
Proteomic Architecture of Human Coronary and Aortic Atherosclerosis.
|
Academic Article
|
Monocyte Polarization is Altered by Total-Body Irradiation in Male Rhesus Macaques: Implications for Delayed Effects of Acute Radiation Exposure.
|
Academic Article
|
Effects of early- and mid-life stress on DNA methylation of genes associated with subclinical cardiovascular disease and cognitive impairment: a systematic review.
|
Grant
|
Integrated Omics Analysis of Pain: Omics Data Generation Center
|
Academic Article
|
Integrative Analysis of Glucometabolic Traits, Adipose Tissue DNA Methylation, and Gene Expression Identifies Epigenetic Regulatory Mechanisms of Insulin Resistance and Obesity in African Americans.
|
Academic Article
|
FADS genetic and metabolomic analyses identify the ?5 desaturase (FADS1) step as a critical control point in the formation of biologically important lipids.
|
Academic Article
|
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
|
Academic Article
|
Intrinsic DNA topology as a prioritization metric in genomic fine-mapping studies.
|
Academic Article
|
Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries.
|
Grant
|
Development of a Wake Forest Multi-Species NHP Biorepository to Support Interdisciplinary Aging Studies
|
Academic Article
|
Genetic Knowledge and Communication Among Mexican Farmworkers and Non-farmworkers in North Carolina.
|