A genome-wide association study of chronic otitis media with effusion and recurrent otitis media identifies a novel susceptibility locus on chromosome 2

JARO - Journal of the Association for Research in Otolaryngology

Volumn 14, Issue 6, 2013, Pages 791-800

  Allen, E Kaitlynn ^a,b   Chen, Wei Min ^a   Weeks, Daniel E ^c,d   Chen, Fang ^a   Hou, Xuanlin ^a   Mattos, José L ^a   Mychaleckyj, Josyf C ^a   Segade, Fernando ^e   Casselbrant, Margaretha L ^f   Mandel, Ellen M ^f   Ferrell, Robert E ^c   Rich, Stephen S ^a   Daly, Kathleen A ^g   Sale, Michèle M ^a,b  

^a UNIVERSITY OF VIRGINIA   (United States)

^b UNIVERSITY OF VIRGINIA   (United States)

^c Department of Public Health Sciences ^*  (United States)

^d UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

^f CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^g UNIVERSITY OF MINNESOTA   (United States)

Author keywords

genetics; genome; locus; otitis media; susceptibility

Indexed keywords

DNA; SPACER DNA;

ARTICLE; CHROMOSOME 15; CHROMOSOME 19; CHROMOSOME 2; CHROMOSOME 5; CHRONIC SECRETORY OTITIS MEDIA; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RECURRENT DISEASE; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOMES, HUMAN, PAIR 2; CHRONIC DISEASE; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; OTITIS MEDIA; OTITIS MEDIA WITH EFFUSION; POLYMORPHISM, SINGLE NUCLEOTIDE; QUANTITATIVE TRAIT LOCI; RECURRENCE;

EID: 84889098463     PISSN: 15253961     EISSN: 14387573     Source Type: Journal    
DOI: 10.1007/s10162-013-0411-2     Document Type: Article

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