BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

275 related articles for article (PubMed ID: 23974705)

  • 1. A genome-wide association study of chronic otitis media with effusion and recurrent otitis media identifies a novel susceptibility locus on chromosome 2.
    Allen EK; Chen WM; Weeks DE; Chen F; Hou X; Mattos JL; Mychaleckyj JC; Segade F; Casselbrant ML; Mandel EM; Ferrell RE; Rich SS; Daly KA; Sale MM
    J Assoc Res Otolaryngol; 2013 Dec; 14(6):791-800. PubMed ID: 23974705
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM).
    Sale MM; Chen WM; Weeks DE; Mychaleckyj JC; Hou X; Marion M; Segade F; Casselbrant ML; Mandel EM; Ferrell RE; Rich SS; Daly KA
    PLoS One; 2011; 6(8):e22297. PubMed ID: 21857919
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study.
    Segade F; Daly KA; Allred D; Hicks PJ; Cox M; Brown M; Hardisty-Hughes RE; Brown SD; Rich SS; Bowden DW
    Arch Otolaryngol Head Neck Surg; 2006 Jul; 132(7):729-33. PubMed ID: 16847180
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Significant linkage at chromosome 19q for otitis media with effusion and/or recurrent otitis media (COME/ROM).
    Chen WM; Allen EK; Mychaleckyj JC; Chen F; Hou X; Rich SS; Daly KA; Sale MM
    BMC Med Genet; 2011 Sep; 12():124. PubMed ID: 21943191
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluation of replication of variants associated with genetic risk of otitis media.
    Allen EK; Manichaikul A; Chen WM; Rich SS; Daly KA; Sale MM
    PLoS One; 2014; 9(8):e104212. PubMed ID: 25089819
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood.
    Rye MS; Warrington NM; Scaman ES; Vijayasekaran S; Coates HL; Anderson D; Pennell CE; Blackwell JM; Jamieson SE
    PLoS One; 2012; 7(10):e48215. PubMed ID: 23133572
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.
    Einarsdottir E; Hafrén L; Leinonen E; Bhutta MF; Kentala E; Kere J; Mattila PS
    Sci Rep; 2016 Sep; 6():33240. PubMed ID: 27632927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic and functional evidence for a locus controlling otitis media at chromosome 10q26.3.
    Rye MS; Scaman ES; Thornton RB; Vijayasekaran S; Coates HL; Francis RW; Pennell CE; Blackwell JM; Jamieson SE
    BMC Med Genet; 2014 Feb; 15():18. PubMed ID: 24499112
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic susceptibility to chronic otitis media with effusion: candidate gene single nucleotide polymorphisms.
    MacArthur CJ; Wilmot B; Wang L; Schuller M; Lighthall J; Trune D
    Laryngoscope; 2014 May; 124(5):1229-35. PubMed ID: 23929584
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chronic and recurrent otitis media: a genome scan for susceptibility loci.
    Daly KA; Brown WM; Segade F; Bowden DW; Keats BJ; Lindgren BR; Levine SC; Rich SS
    Am J Hum Genet; 2004 Dec; 75(6):988-97. PubMed ID: 15514890
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions.
    Casselbrant ML; Mandel EM; Jung J; Ferrell RE; Tekely K; Szatkiewicz JP; Ray A; Weeks DE
    BMC Med Genet; 2009 Sep; 10():85. PubMed ID: 19728873
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Endometrial vezatin and its association with endometriosis risk.
    Holdsworth-Carson SJ; Fung JN; Luong HT; Sapkota Y; Bowdler LM; Wallace L; Teh WT; Powell JE; Girling JE; Healey M; Montgomery GW; Rogers PA
    Hum Reprod; 2016 May; 31(5):999-1013. PubMed ID: 27005890
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic background and the risk of otitis media.
    Hafrén L; Kentala E; Järvinen TM; Leinonen E; Onkamo P; Kere J; Mattila PS
    Int J Pediatr Otorhinolaryngol; 2012 Jan; 76(1):41-4. PubMed ID: 22018929
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.
    Johnson MP; Brennecke SP; East CE; Göring HH; Kent JW; Dyer TD; Said JM; Roten LT; Iversen AC; Abraham LJ; Heinonen S; Kajantie E; Kere J; Kivinen K; Pouta A; Laivuori H; ; Austgulen R; Blangero J; Moses EK
    PLoS One; 2012; 7(3):e33666. PubMed ID: 22432041
    [TBL] [Abstract][Full Text] [Related]  

  • 15. FBXO11, a regulator of the TGFβ pathway, is associated with severe otitis media in Western Australian children.
    Rye MS; Wiertsema SP; Scaman ES; Oommen J; Sun W; Francis RW; Ang W; Pennell CE; Burgner D; Richmond P; Vijayasekaran S; Coates HL; Brown SD; Blackwell JM; Jamieson SE
    Genes Immun; 2011 Jul; 12(5):352-9. PubMed ID: 21293382
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide association analyses identify known and novel loci for teat number in Duroc pigs using single-locus and multi-locus models.
    Zhuang Z; Ding R; Peng L; Wu J; Ye Y; Zhou S; Wang X; Quan J; Zheng E; Cai G; Huang W; Yang J; Wu Z
    BMC Genomics; 2020 May; 21(1):344. PubMed ID: 32380955
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A variant on chromosome 2p13.3 is associated with atopic dermatitis in Chinese Han population.
    Cai XY; Zheng XD; Fang L; Zhou FS; Sheng YJ; Wu YY; Yu CX; Zhu J; Xiao FL
    Gene; 2017 Sep; 628():281-285. PubMed ID: 28739399
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility Locus.
    Mitchell AL; Bøe Wolff A; MacArthur K; Weaver JU; Vaidya B; ; Erichsen MM; Darlay R; Husebye ES; Cordell HJ; Pearce SH
    PLoS One; 2015; 10(6):e0123550. PubMed ID: 26042420
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of ISL1 polymorphisms and eosinophilic levels among otitis media patients.
    Kondyarpu A; Ray CS; Panda KC; Biswal NC; Ramchander PV
    J Clin Lab Anal; 2021 Mar; 35(3):e23702. PubMed ID: 33476445
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomewide association study identifies HAS2 as a novel susceptibility gene for adult asthma in a Japanese population.
    Yatagai Y; Sakamoto T; Yamada H; Masuko H; Kaneko Y; Iijima H; Naito T; Noguchi E; Hirota T; Tamari M; Konno S; Nishimura M; Hizawa N
    Clin Exp Allergy; 2014 Nov; 44(11):1327-34. PubMed ID: 25251750
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.