DNA sequence variants in genes involved in the innate immune response and secondary response to infection may confer susceptibility to chronic otitis media with effusion and/or recurrent otitis media (COME/ROM). We evaluated single nucleotide polymorphisms (SNPs) in 15 functional candidate genes. A total of 99 SNPs were successfully genotyped on the Sequenom platform in 142 families (618 subjects) from the Minnesota COME/ROM Family Study. Data were analyzed for association with COME/ROM using the Generalized Disequilibrium Test (GDT). Sex and age at exam were adjusted as covariates, relatedness was accounted for, and genotype differences from all phenotypically discordant relative pairs were utilized to measure the evidence of association b...
Contains fulltext : 51717.pdf (publisher's version ) (Open Access)OBJECTIVE: Cytok...
Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and ...
To identify genetic risk factors of childhood otitis media (OM), a genome-wide association study was...
DNA sequence variants in genes involved in the innate immune response and secondary response to infe...
DNA sequence variants in genes involved in the innate immune response and secondary response to infe...
The first Genome Wide Association Study (GWAS) of otitis media (OM) found evidence of association in...
Evaluation of the genetic contribution to the development of recurrent acute otitis media (rAOM) rem...
Acute otitis media (OM) is a common disease which often develops through complex interactions betwee...
Background: Otitis media (OM) is a common childhood disease characterised by middle ear inflammation...
BACKGROUND: Otitis media (OM) is a common childhood disease characterised by middle ear inflammation...
Acute otitis media (OM) is a common disease which often develops through complex interactions betwee...
<div><h3>Background</h3><p>Otitis media (OM) is a common childhood disease characterised by middle e...
Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and ...
OBJECTIVE. Cytokines and other inflammatory mediators are involved in the pathogenesis of otitis med...
Otitis media (OM) is the most common childhood disease. Almost all children experience at least one ...
Contains fulltext : 51717.pdf (publisher's version ) (Open Access)OBJECTIVE: Cytok...
Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and ...
To identify genetic risk factors of childhood otitis media (OM), a genome-wide association study was...
DNA sequence variants in genes involved in the innate immune response and secondary response to infe...
DNA sequence variants in genes involved in the innate immune response and secondary response to infe...
The first Genome Wide Association Study (GWAS) of otitis media (OM) found evidence of association in...
Evaluation of the genetic contribution to the development of recurrent acute otitis media (rAOM) rem...
Acute otitis media (OM) is a common disease which often develops through complex interactions betwee...
Background: Otitis media (OM) is a common childhood disease characterised by middle ear inflammation...
BACKGROUND: Otitis media (OM) is a common childhood disease characterised by middle ear inflammation...
Acute otitis media (OM) is a common disease which often develops through complex interactions betwee...
<div><h3>Background</h3><p>Otitis media (OM) is a common childhood disease characterised by middle e...
Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and ...
OBJECTIVE. Cytokines and other inflammatory mediators are involved in the pathogenesis of otitis med...
Otitis media (OM) is the most common childhood disease. Almost all children experience at least one ...
Contains fulltext : 51717.pdf (publisher's version ) (Open Access)OBJECTIVE: Cytok...
Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and ...
To identify genetic risk factors of childhood otitis media (OM), a genome-wide association study was...