Item Type | Name |
Concept
|
Aged, 80 and over
|
Concept
|
Autophagy
|
Concept
|
Adaptation, Physiological
|
Concept
|
Abnormalities, Multiple
|
Concept
|
Aged
|
Concept
|
Amino Acids
|
Concept
|
Amino Acid Sequence
|
Concept
|
Bronchodilator Agents
|
Concept
|
Anticoagulants
|
Concept
|
Chromosomes, Human, Pair 11
|
Concept
|
Chromosomes, Human, Pair 2
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Chromosomes, Human, Pair 8
|
Concept
|
Asthma
|
Concept
|
Autoimmune Diseases
|
Concept
|
Aryl Hydrocarbon Hydroxylases
|
Concept
|
Base Sequence
|
Concept
|
Bayes Theorem
|
Concept
|
Pan troglodytes
|
Concept
|
Binding Sites
|
Concept
|
Chromosomes, Human, Pair 1
|
Concept
|
Chromosomes, Human, Pair 15
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Coenzyme A
|
Concept
|
Colon
|
Concept
|
Child Day Care Centers
|
Concept
|
Chromosomes, Human, Pair 12
|
Concept
|
Chromosomes, Human, Pair 14
|
Concept
|
Chicago
|
Concept
|
Chromosomes, Human, Pair 13
|
Concept
|
Chromosomes, Human, Pair 4
|
Concept
|
Chromosomes, Human, Pair 5
|
Concept
|
Craniofacial Dysostosis
|
Concept
|
Hemoglobins
|
Concept
|
Diabetes Mellitus, Type 1
|
Concept
|
Diabetes Mellitus, Type 2
|
Concept
|
Dermatitis, Atopic
|
Concept
|
Diabetic Nephropathies
|
Concept
|
Immunoglobulin Constant Regions
|
Concept
|
Cytidine Deaminase
|
Concept
|
Cytoskeleton
|
Concept
|
DNA Repair
|
Concept
|
Kallikreins
|
Concept
|
Endocarditis, Bacterial
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 17
|
Concept
|
Chromosomes, Human, Pair 19
|
Concept
|
Exons
|
Concept
|
Erythropoietin
|
Concept
|
Costa Rica
|
Concept
|
Cross-Sectional Studies
|
Concept
|
Disease Susceptibility
|
Concept
|
Indoles
|
Concept
|
Micrognathism
|
Concept
|
Deamination
|
Concept
|
Myosin-Light-Chain Kinase
|
Concept
|
Genetics
|
Concept
|
Obesity
|
Concept
|
DNA Replication
|
Concept
|
Immunoglobulin Heavy Chains
|
Concept
|
Interleukin-1
|
Concept
|
Genetics, Population
|
Concept
|
Leukocytes, Mononuclear
|
Concept
|
Meningitis, Pneumococcal
|
Concept
|
Leukocytes
|
Concept
|
Immunoglobulin E
|
Concept
|
Pharmacogenetics
|
Concept
|
Mice, Transgenic
|
Concept
|
Immunohistochemistry
|
Concept
|
Puerto Rico
|
Concept
|
Mice, Inbred C57BL
|
Concept
|
Middle Aged
|
Concept
|
HeLa Cells
|
Concept
|
Lipopolysaccharides
|
Concept
|
Nuclear Family
|
Concept
|
Fetal Blood
|
Concept
|
Genetic Markers
|
Concept
|
Intestinal Mucosa
|
Concept
|
Intestine, Small
|
Concept
|
Rhode Island
|
Concept
|
Cohort Studies
|
Concept
|
Smoking
|
Concept
|
Stress, Psychological
|
Concept
|
Texas
|
Concept
|
Synaptic Membranes
|
Concept
|
Humans
|
Concept
|
Body Mass Index
|
Concept
|
Transcription, Genetic
|
Concept
|
Smoking Cessation
|
Concept
|
United States
|
Concept
|
Biomarkers, Tumor
|
Concept
|
Tumor Necrosis Factor-alpha
|
Concept
|
Tobacco Smoke Pollution
|
Concept
|
Warfarin
|
Concept
|
Histocompatibility Antigens Class I
|
Concept
|
Biomarkers
|
Concept
|
Electrophoretic Mobility Shift Assay
|
Concept
|
Mexico
|
Concept
|
Mandibulofacial Dysostosis
|
Concept
|
CD4-Positive T-Lymphocytes
|
Concept
|
Interleukin-8
|
Concept
|
Case-Control Studies
|
Concept
|
Prostate-Specific Antigen
|
Concept
|
Protein Structure, Tertiary
|
Concept
|
Limb Deformities, Congenital
|
Concept
|
NADH Dehydrogenase
|
Concept
|
North America
|
Concept
|
Bronchial Hyperreactivity
|
Concept
|
Mice, Knockout
|
Concept
|
Receptors, Adrenergic, beta-2
|
Concept
|
Chemokines, CC
|
Concept
|
Chemokine CXCL12
|
Concept
|
CpG Islands
|
Concept
|
Exome
|
Concept
|
Proteomics
|
Concept
|
Histone Code
|
Concept
|
Cortactin
|
Concept
|
Kringles
|
Concept
|
5' Untranslated Regions
|
Concept
|
Parents
|
Concept
|
3' Untranslated Regions
|
Concept
|
Nod1 Signaling Adaptor Protein
|
Concept
|
Databases, Genetic
|
Concept
|
Information Dissemination
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Mice
|
Concept
|
RNA, Ribosomal, 16S
|
Concept
|
Saccharomyces cerevisiae
|
Concept
|
South Dakota
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Down-Regulation
|
Concept
|
Multivariate Analysis
|
Concept
|
Open Reading Frames
|
Concept
|
Laser Coagulation
|
Concept
|
DNA Methylation
|
Concept
|
Caribbean Region
|
Concept
|
Molecular Epidemiology
|
Concept
|
Proto-Oncogene Proteins c-met
|
Concept
|
Genes, erbB-2
|
Concept
|
Interleukin-13
|
Concept
|
Untranslated Regions
|
Concept
|
Kv Channel-Interacting Proteins
|
Concept
|
Smad2 Protein
|
Concept
|
Transcriptome
|
Concept
|
HLA-DRB1 Chains
|
Concept
|
Nod2 Signaling Adaptor Protein
|
Concept
|
DNA Mismatch Repair
|
Concept
|
Metabolomics
|
Concept
|
Siblings
|
Concept
|
HLA-G Antigens
|
Concept
|
Cytosine Deaminase
|
Concept
|
Blood Chemical Analysis
|
Concept
|
Calcium-Binding Proteins
|
Concept
|
Canada
|
Concept
|
Chromatin
|
Concept
|
Chromosomes, Human, Pair 16
|
Concept
|
Chromosomes, Human, Pair 18
|
Concept
|
Colitis, Ulcerative
|
Concept
|
Data Interpretation, Statistical
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Immunoglobulins
|
Concept
|
Lymphocytes
|
Concept
|
Peptidoglycan
|
Concept
|
Phylogeny
|
Concept
|
Prospective Studies
|
Concept
|
Retrospective Studies
|
Concept
|
Signal Transduction
|
Concept
|
Tumor Suppressor Protein p53
|
Concept
|
Age of Onset
|
Concept
|
Maternal Exposure
|
Concept
|
Computational Biology
|
Concept
|
Physical Chromosome Mapping
|
Concept
|
Genomics
|
Concept
|
MicroRNAs
|
Concept
|
Angiopoietins
|
Concept
|
Adipokines
|
Concept
|
Young Adult
|
Academic Article
|
Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.
|
Academic Article
|
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.
|
Academic Article
|
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.
|
Academic Article
|
Effect of subcutaneous recombinant human erythropoietin in cancer patients receiving radiotherapy: final report of a randomized, open-labelled, phase II trial.
|
Academic Article
|
Effects of sequence and structure on the hypermutability of immunoglobulin genes.
|
Academic Article
|
On a randomization procedure.
|
Academic Article
|
Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan.
|
Academic Article
|
Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure.
|
Academic Article
|
Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy.
|
Academic Article
|
Rapid divergence in expression between duplicate genes inferred from microarray data.
|
Academic Article
|
Measuring the relative information in allele-sharing linkage studies.
|
Academic Article
|
MERLIN...and the geneticist's stone?
|
Academic Article
|
Somatic hypermutation and class switch recombination in Msh6(-/-)Ung(-/-) double-knockout mice.
|
Academic Article
|
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
Academic Article
|
Regulation of IL-8 and IL-1beta expression in Crohn's disease associated NOD2/CARD15 mutations.
|
Academic Article
|
Association studies for untyped markers with TUNA.
|
Academic Article
|
Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set.
|
Academic Article
|
Dominant-negative TLR5 polymorphism reduces adaptive immune response to flagellin and negatively associates with Crohn's disease.
|
Academic Article
|
A genome scan in 260 inflammatory bowel disease-affected relative pairs.
|
Academic Article
|
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
Academic Article
|
A common cortactin gene variation confers differential susceptibility to severe asthma.
|
Academic Article
|
Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.
|
Academic Article
|
Testing untyped alleles (TUNA)-applications to genome-wide association studies.
|
Academic Article
|
Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans.
|
Academic Article
|
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
|
Academic Article
|
Phenotype-stratified genetic linkage study demonstrates that IBD2 is an extensive ulcerative colitis locus.
|
Academic Article
|
Ethnic differences and functional analysis of MET mutations in lung cancer.
|
Academic Article
|
Somatic hypermutation: processivity of the cytosine deaminase AID and error-free repair of the resulting uracils.
|
Academic Article
|
Smoking and inflammatory bowel disease: trends in familial and sporadic cohorts.
|
Academic Article
|
Invasive pneumococcal infections: Austrian syndrome.
|
Academic Article
|
SCAN: SNP and copy number annotation.
|
Academic Article
|
Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.
|
Academic Article
|
Allele-specific targeting of microRNAs to HLA-G and risk of asthma.
|
Academic Article
|
The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans.
|
Academic Article
|
Integrin beta 3 genotype influences asthma and allergy phenotypes in the first 6 years of life.
|
Academic Article
|
Restricted parameter space models for testing gene-gene interaction.
|
Academic Article
|
You've gotta be lucky: Coverage and the elusive gene-gene interaction.
|
Academic Article
|
An evolutionary framework for association testing in resequencing studies.
|
Academic Article
|
Genome-wide meta-analysis for severe diabetic retinopathy.
|
Academic Article
|
Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects.
|
Academic Article
|
Increased protein-coding mutations in the mitochondrial genome of African American women with preeclampsia.
|
Academic Article
|
Finding disease variants in Mendelian disorders by using sequence data: methods and applications.
|
Academic Article
|
Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases.
|
Academic Article
|
Patient self-report of prior laser treatment reliably indicates presence of severe diabetic retinopathy.
|
Academic Article
|
Resequencing candidate genes implicates rare variants in asthma susceptibility.
|
Academic Article
|
Quantifying the amount of missing information in genetic association studies.
|
Academic Article
|
Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function.
|
Academic Article
|
Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors.
|
Academic Article
|
A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose.
|
Academic Article
|
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
|
Academic Article
|
Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease.
|
Academic Article
|
Association studies for asthma and atopic diseases: a comprehensive review of the literature.
|
Academic Article
|
A genome scan in 260 inflammatory bowel disease-affected relative pairs.
|
Academic Article
|
Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
|
Academic Article
|
Gene-environment interaction effects on the development of immune responses in the 1st year of life.
|
Academic Article
|
The very 5' end and the constant region of Ig genes are spared from somatic mutation because AID does not access these regions.
|
Academic Article
|
GEL: a novel genotype calling algorithm using empirical likelihood.
|
Academic Article
|
A signature of evolutionary constraint on a subset of ectopically expressed olfactory receptor genes.
|
Academic Article
|
(Too) great expectations: the challenges in replicating asthma disease genes.
|
Academic Article
|
Common variants at five new loci associated with early-onset inflammatory bowel disease.
|
Academic Article
|
The pattern of somatic hypermutation of Ig genes is altered when p53 is inactivated.
|
Academic Article
|
Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European Americans.
|
Academic Article
|
Rhinovirus wheezing illness and genetic risk of childhood-onset asthma.
|
Academic Article
|
A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations.
|
Academic Article
|
Maternal asthma and microRNA regulation of soluble HLA-G in the airway.
|
Academic Article
|
A genome-wide survey of CD4(+) lymphocyte regulatory genetic variants identifies novel asthma genes.
|
Academic Article
|
A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.
|
Academic Article
|
Genome-wide interaction studies reveal sex-specific asthma risk alleles.
|
Academic Article
|
Ethnicity-specific pharmacogenetics: the case of warfarin in African Americans.
|
Academic Article
|
PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population.
|
Academic Article
|
Genome-wide association study of lung function phenotypes in a founder population.
|
Academic Article
|
Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma.
|
Academic Article
|
Noninvasive analysis of the sputum transcriptome discriminates clinical phenotypes of asthma.
|
Academic Article
|
Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos.
|
Academic Article
|
Stress and Bronchodilator Response in Children with Asthma.
|
Academic Article
|
A gene-based association method for mapping traits using reference transcriptome data.
|
Academic Article
|
Genome-wide association study of recalcitrant atopic dermatitis in Korean children.
|
Academic Article
|
Genetic associations with viral respiratory illnesses and asthma control inĀ children.
|
Academic Article
|
Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways.
|
Academic Article
|
Noninvasive Analysis of the Sputum Transcriptome Discriminates Clinical Phenotypes of Asthma.
|
Academic Article
|
Association Tests for Rare Variants.
|
Academic Article
|
A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome.
|
Academic Article
|
Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.
|
Academic Article
|
DNA methylation in lung cells is associated with asthma endotypes and genetic risk.
|
Academic Article
|
Gene Expression Profiling in Blood Provides Reproducible Molecular Insights into Asthma Control.
|
Academic Article
|
Host genetic variation in mucosal immunity pathways influences the upper airway microbiome.
|
Academic Article
|
Rare non-coding variants are associated with plasma lipid traits in a founder population.
|
Academic Article
|
An admixture mapping meta-analysis implicates genetic variation at 18q21 with asthma susceptibility in Latinos.
|
Academic Article
|
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.
|
Academic Article
|
Role of local CpG DNA methylation in mediating the 17q21 asthma susceptibility gasdermin B (GSDMB)/ORMDL sphingolipid biosynthesis regulator 3 (ORMDL3) expression quantitative trait locus.
|
Academic Article
|
A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle.
|
Academic Article
|
Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions.
|
Academic Article
|
Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.
|
Academic Article
|
Gene Coexpression Networks in Whole Blood Implicate Multiple Interrelated Molecular Pathways in Obesity in People with Asthma.
|
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
|
Integrating predicted transcriptome from multiple tissues improves association detection.
|
Academic Article
|
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.
|
Academic Article
|
Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.
|
Academic Article
|
Accounting for unobserved covariates with varying degrees of estimability in high-dimensional biological data.
|
Academic Article
|
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree.
|
Academic Article
|
Association of HLA-DRB1*09:01 with tIgE levels among African-ancestry individuals with asthma.
|
Academic Article
|
Expression quantitative trait locus fine mapping of the 17q12-21 asthma locus in African American children: a genetic association and gene expression study.
|
Academic Article
|
Epigenetic landscape links upper airway microbiota in infancy with allergic rhinitis at 6 years of age.
|
Academic Article
|
Altered transcriptional and chromatin responses to rhinovirus in bronchial epithelial cells from adults with asthma.
|
Academic Article
|
Chromosome 17q12-21 Variants Are Associated with Multiple Wheezing Phenotypes in Childhood.
|
Academic Article
|
Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus.
|
Academic Article
|
Fine-mapping studies distinguish genetic risks for childhood- and adult-onset asthma in the HLA region.
|
Academic Article
|
Building Programs to Eradicate Toxoplasmosis Part IV: Understanding and Development of Public Health Strategies and Advances "Take a Village".
|
Academic Article
|
Building Programs to Eradicate Toxoplasmosis Part I: Introduction and Overview.
|
Academic Article
|
Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings.
|
Concept
|
Sexism
|
Concept
|
Microbiota
|
Concept
|
Cytochrome P-450 CYP2C9
|
Academic Article
|
Building Programs to Eradicate Toxoplasmosis Part II: Education.
|
Academic Article
|
Epigenetic responses to rhinovirus exposure in airway epithelial cells are correlated with key transcriptional pathways in chronic rhinosinusitis.
|