scholarly article | Q13442814 |
P50 | author | Hakon Hakonarson | Q30003940 |
P2093 | author name string | Michael E March | |
Patrick Ma Sleiman | |||
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CD14and Toll-like Receptor Gene Polymorphisms, Country Living, and Asthma in Adults | Q56893552 | ||
Association analysis of common variants of STAT6, GATA3, and STAT4 to asthma and high serum IgE phenotypes | Q57232742 | ||
Eotaxin polymorphisms and serum total IgE levels in children with asthma | Q58033504 | ||
Gene-gene interaction in regulatory T–cell function in atopy and asthma development in childhood | Q58051790 | ||
Asthma and atopy are associated with chromosome 17q21 markers in Chinese children | Q58492765 | ||
Epigenetic changes in B lymphocytes associated with house dust mite allergic asthma | Q62049975 | ||
A population-based study of bronchial asthma in adult twin pairs | Q70212723 | ||
Genetics of beta 2-adrenergic receptor variants in asthma | Q70974576 | ||
Evidence for a locus regulating total serum IgE levels mapping to chromosome 5 | Q72462711 | ||
Serum total IgE levels and CD14 on chromosome 5q31 | Q73073498 | ||
Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis | Q21145893 | ||
Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function | Q24319020 | ||
TBX21: a functional variant predicts improvement in asthma with the use of inhaled corticosteroids | Q24558608 | ||
Association between genetic polymorphisms of the beta2-adrenoceptor and response to albuterol in children with and without a history of wheezing | Q24561362 | ||
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci | Q24618592 | ||
The role of LTA4H and ALOX5AP genes in the risk for asthma in Latinos | Q24626218 | ||
Genome-wide association study identifies five loci associated with lung function | Q24629653 | ||
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function | Q24633262 | ||
T-bet polymorphisms are associated with asthma and airway hyperresponsiveness | Q24650376 | ||
IRAK-M is involved in the pathogenesis of early-onset persistent asthma | Q24670024 | ||
A new Groucho TLE4 protein may regulate the repressive activity of Pax5 in human B lymphocytes | Q24682733 | ||
Association studies for asthma and atopic diseases: a comprehensive review of the literature | Q24802474 | ||
Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness | Q28214089 | ||
Genetic variants of GSNOR and ADRB2 influence response to albuterol in African-American children with severe asthma | Q28248002 | ||
Characterization of a common susceptibility locus for asthma-related traits | Q28255640 | ||
Downstream target genes of the neuropeptide S-NPSR1 pathway | Q28259421 | ||
A polymorphism controlling ORMDL3 expression is associated with asthma that is poorly controlled by current medications | Q28275529 | ||
A large-scale, consortium-based genomewide association study of asthma | Q28293885 | ||
Genetic susceptibility to asthma--bronchial hyperresponsiveness coinherited with a major gene for atopy | Q28296979 | ||
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis | Q28303063 | ||
Filaggrin null mutations are associated with increased asthma severity in children and young adults | Q28303991 | ||
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction | Q28308221 | ||
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene | Q28943322 | ||
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order | Q28943336 | ||
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population | Q28943340 | ||
Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations | Q28943502 | ||
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis | Q29417041 | ||
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma | Q29417065 | ||
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations | Q29417104 | ||
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma | Q29614903 | ||
The global burden of asthma: executive summary of the GINA Dissemination Committee report | Q29614904 | ||
IL-13 R130Q, a common variant associated with allergy and asthma, enhances effector mechanisms essential for human allergic inflammation | Q30448616 | ||
Worldwide trends in the prevalence of asthma symptoms: phase III of the International Study of Asthma and Allergies in Childhood (ISAAC) | Q30480797 | ||
Analyses of associations between three positionally cloned asthma candidate genes and asthma or asthma-related phenotypes in a Chinese population | Q30936794 | ||
Influence of leukotriene pathway polymorphisms on response to montelukast in asthma | Q33227414 | ||
Toll-like receptor heterodimer variants protect from childhood asthma | Q33343143 | ||
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus | Q33375065 | ||
Assessing the reproducibility of asthma candidate gene associations, using genome-wide data | Q33415299 | ||
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. | Q33419815 | ||
A genome-wide association study of pulmonary function measures in the Framingham Heart Study | Q33419839 | ||
TBX21 gene variants increase childhood asthma risk in combination with HLX1 variants | Q33429396 | ||
A graphical model approach for inferring large-scale networks integrating gene expression and genetic polymorphism | Q33453997 | ||
Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children | Q33497893 | ||
Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions | Q33669033 | ||
Variants in FAM13A are associated with chronic obstructive pulmonary disease | Q33687879 | ||
The IL12B gene is associated with asthma | Q33910222 | ||
Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21 | Q33938575 | ||
Effect of beta2-adrenergic receptor polymorphism on response to longacting beta2 agonist in asthma (LARGE trial): a genotype-stratified, randomised, placebo-controlled, crossover trial | Q34038869 | ||
Gene-environment interactions influence airways function in laboratory animal workers | Q34050109 | ||
Variants of DENND1B associated with asthma in children | Q34089817 | ||
A second-generation genomewide screen for asthma-susceptibility alleles in a founder population | Q34146748 | ||
Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma | Q34198087 | ||
Positional cloning of a novel gene influencing asthma from chromosome 2q14. | Q34270888 | ||
Corticosteroid pharmacogenetics: association of sequence variants in CRHR1 with improved lung function in asthmatics treated with inhaled corticosteroids | Q34318910 | ||
Asthma genetics 2006: the long and winding road to gene discovery. | Q34482054 | ||
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. | Q34489270 | ||
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia | Q34694697 | ||
ORMDL3 gene is associated with asthma in three ethnically diverse populations | Q34756865 | ||
Identification of a novel asthma susceptibility gene on chromosome 1qter and its functional evaluation. | Q34762179 | ||
The glucocorticoid receptor heterocomplex gene STIP1 is associated with improved lung function in asthmatic subjects treated with inhaled corticosteroids | Q35051364 | ||
PDE11A associations with asthma: results of a genome-wide association scan | Q35096782 | ||
Asthma exacerbations during long term beta agonist use: influence of beta(2) adrenoceptor polymorphism | Q35534065 | ||
Allelic association and functional studies of promoter polymorphism in the leukotriene C4 synthase gene (LTC4S) in asthma | Q35535893 | ||
Recent development in genomic and proteomic research for asthma | Q35641964 | ||
Resequencing candidate genes implicates rare variants in asthma susceptibility | Q35748389 | ||
Association of defensin beta-1 gene polymorphisms with asthma | Q35761951 | ||
A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study | Q35802982 | ||
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. | Q35816887 | ||
Evidence for Mendelian inheritance of serum IgE levels in Hispanic and non-Hispanic white families | Q35889674 | ||
Genome-wide association study of lung function decline in adults with and without asthma | Q35923186 | ||
Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function | Q36099476 | ||
Recent advances in asthma genetics | Q36462660 | ||
Toward a comprehensive set of asthma susceptibility genes | Q36565021 | ||
Interleukin-18 genetics and inflammatory disease susceptibility | Q36704477 | ||
A genome-wide association study on African-ancestry populations for asthma | Q36709708 | ||
Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma | Q36886258 | ||
Effect of ADRB2 polymorphisms on response to longacting beta2-agonist therapy: a pharmacogenetic analysis of two randomised studies | Q37044226 | ||
Discovering susceptibility genes for asthma and allergy | Q37095239 | ||
Clinical consequences of ADRbeta2 polymorphisms | Q37096063 | ||
Role and pharmacogenomics of TNF-alpha in asthma | Q37240028 | ||
Genetic variability of the high-affinity IgE receptor alpha-subunit (FcepsilonRIalpha). | Q37251955 | ||
Gene-gene interaction in asthma: IL4RA and IL13 in a Dutch population with asthma | Q37360189 | ||
Leukotriene pathway genetics and pharmacogenetics in allergy. | Q37470762 | ||
Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility | Q37699224 | ||
Nitrative stress in inflammatory lung diseases | Q37858170 | ||
An association between IL-9 and IL-9 receptor gene polymorphisms and atopic dermatitis in a Korean population | Q39775898 | ||
NOD1 variation, immunoglobulin E and asthma. | Q40457038 | ||
Association between exposure to farming, allergies and genetic variation in CARD4/NOD1. | Q40471979 | ||
Toll-like receptor 2 as a major gene for asthma in children of European farmers | Q40538810 | ||
Association of a promoter polymorphism of the CD14 gene and atopy | Q40605259 | ||
Genetics of asthma and hay fever in Australian twins. | Q40755776 | ||
A screening methodology based on Random Forests to improve the detection of gene-gene interactions | Q41733505 | ||
IL-4/IL-13 pathway genetics strongly influence serum IgE levels and childhood asthma | Q42679779 | ||
Evidence for two unlinked loci regulating total serum IgE levels | Q42950780 | ||
TLR-related pathway analysis: novel gene-gene interactions in the development of asthma and atopy. | Q43454514 | ||
Chromosome 17q21 gene variants are associated with asthma and exacerbations but not atopy in early childhood. | Q44053079 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 3.0 Unported | Q18810331 |
P6216 | copyright status | copyrighted | Q50423863 |
P407 | language of work or name | English | Q1860 |
P921 | main subject | asthma | Q35869 |
asthma genetics | Q125760026 | ||
P304 | page(s) | 253-265 | |
P577 | publication date | 2013-04-17 | |
P1433 | published in | International Journal of General Medicine | Q6051402 |
P1476 | title | Genetic polymorphisms and associated susceptibility to asthma | |
P478 | volume | 6 |
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