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Journal Abstract Search

203 related items for PubMed ID: 16918960

  • 21. Genetic developments in autoimmune thyroid disease: an evolutionary process.
    Zeitlin AA, Simmonds MJ, Gough SC.
    Clin Endocrinol (Oxf); 2008 May; 68(5):671-82. PubMed ID: 18081880
    [Abstract] [Full Text] [Related]

  • 22. Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children.
    Amre DK, Mack D, Israel D, Morgan K, Lambrette P, Law L, Grimard G, Deslandres C, Krupoves A, Bucionis V, Costea I, Bissonauth V, Feguery H, D'Souza S, Levy E, Seidman EG.
    Am J Gastroenterol; 2008 Mar; 103(3):615-20. PubMed ID: 18047539
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  • 23. Association between interleukin 21 and Graves' disease.
    Jia HY, Zhang ZG, Gu XJ, Guo T, Cui B, Ning G, Zhao YJ.
    Genet Mol Res; 2011 Oct 31; 10(4):3338-46. PubMed ID: 22057994
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  • 24. Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population.
    Santiago JL, Martínez A, de la Calle H, Fernández-Arquero M, Figueredo MA, de la Concha EG, Urcelay E.
    BMC Med Genet; 2007 Aug 13; 8():54. PubMed ID: 17697317
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  • 25. Detailed analysis of the relative power of direct and indirect association studies and the implications for their interpretation.
    Moskvina V, O'Donovan MC.
    Hum Hered; 2007 Aug 13; 64(1):63-73. PubMed ID: 17483598
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  • 29. Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.
    Qiu XS, Tang NL, Yeung HY, Lee KM, Hung VW, Ng BK, Ma SL, Kwok RH, Qin L, Qiu Y, Cheng JC.
    Spine (Phila Pa 1976); 2007 Jul 15; 32(16):1748-53. PubMed ID: 17632395
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  • 30. Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.
    Amre DK, Mack DR, Morgan K, Fujiwara M, Israel D, Deslandres C, Seidman EG, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Levy E.
    Am J Gastroenterol; 2009 Nov 15; 104(11):2824-8. PubMed ID: 19623168
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  • 31. Extensive genotyping of the BDNF and NTRK2 genes define protective haplotypes against obsessive-compulsive disorder.
    Alonso P, Gratacòs M, Menchón JM, Saiz-Ruiz J, Segalàs C, Baca-García E, Labad J, Fernández-Piqueras J, Real E, Vaquero C, Pérez M, Dolengevich H, González JR, Bayés M, de Cid R, Vallejo J, Estivill X.
    Biol Psychiatry; 2008 Mar 15; 63(6):619-28. PubMed ID: 17884018
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  • 32. Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population.
    Lamsyah H, Rueda B, Baassi L, Elaouad R, Bottini N, Sadki K, Martin J.
    Tissue Antigens; 2009 Sep 15; 74(3):228-32. PubMed ID: 19563523
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  • 33. A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population.
    Núñez C, López-Mejías R, Martínez A, García-Rodríguez MC, Fernández-Arquero M, de la Concha EG, Urcelay E.
    BMC Med Genet; 2006 Mar 15; 7():25. PubMed ID: 16539704
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  • 35. Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease.
    Amre DK, Mack DR, Morgan K, Israel D, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Deslandres C, Levy E, Seidman EG.
    Aliment Pharmacol Ther; 2009 May 01; 29(9):1025-31. PubMed ID: 19210299
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  • 37. The functional R620W variant of the PTPN22 gene is associated with celiac disease.
    Santin I, Castellanos-Rubio A, Aransay AM, Castaño L, Vitoria JC, Bilbao JR.
    Tissue Antigens; 2008 Mar 01; 71(3):247-9. PubMed ID: 18194365
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  • 38. Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.
    Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C.
    Hum Mol Genet; 2007 Apr 15; 16(8):887-99. PubMed ID: 17324965
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  • 39. CTLA4 polymorphisms and ophthalmopathy in Graves' disease patients: association study and meta-analysis.
    Han S, Zhang S, Zhang W, Li R, Li Y, Wang Z, Xie Y, Mao Y.
    Hum Immunol; 2006 Aug 15; 67(8):618-26. PubMed ID: 16916658
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  • 40. Association of a thyroglobulin gene polymorphism with Hashimoto's thyroiditis in the Japanese population.
    Ban Y, Tozaki T, Taniyama M, Tomita M, Ban Y.
    Clin Endocrinol (Oxf); 2004 Aug 15; 61(2):263-8. PubMed ID: 15272924
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