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Journal Abstract Search

166 related items for PubMed ID: 32111053

  • 21. Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.
    Zuvich RL, McCauley JL, Oksenberg JR, Sawcer SJ, De Jager PL, International Multiple Sclerosis Genetics Consortium, Aubin C, Cross AH, Piccio L, Aggarwal NT, Evans D, Hafler DA, Compston A, Hauser SL, Pericak-Vance MA, Haines JL.
    Hum Genet; 2010 Mar; 127(5):525-35. PubMed ID: 20112030
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  • 23. Meta-analysis of the Selected Genetic Variants in Immune-Related Genes and Multiple Sclerosis Risk.
    Zhou W, Hu W, Tang L, Ma X, Liao J, Yu Z, Qi M, Chen B, Li J.
    Mol Neurobiol; 2024 Oct; 61(10):8175-8187. PubMed ID: 38478144
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  • 27. [The effect of genetic factors on the phenotypic expression of multiple sclerosis].
    Korobko DS, Malkova NA, Bulatova EV, Babenko LA, Sazonov DV, Sokolova EA, Filipenko ML.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2013 Oct; 113(2 Pt 2):10-6. PubMed ID: 23528589
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  • 28. The influence of non-HLA gene polymorphisms and interactions on disease risk in a Western Australian multiple sclerosis cohort.
    Qiu W, Pham K, James I, Nolan D, Castley A, Christiansen FT, Czarniak P, Luo Y, Wu J, Garlepp M, Wilton S, Carroll WM, Mastaglia FL, Kermode AG.
    J Neuroimmunol; 2013 Aug 15; 261(1-2):92-7. PubMed ID: 23726763
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  • 29. Association between the IL7R T244I polymorphism and multiple sclerosis risk: a meta analysis.
    Wu S, Liu Q, Zhu JM, Wang MR, Li J, Sun MG.
    Neurol Sci; 2016 Sep 15; 37(9):1467-74. PubMed ID: 27188999
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  • 30. Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.
    Hoppenbrouwers IA, Aulchenko YS, Janssens AC, Ramagopalan SV, Broer L, Kayser M, Ebers GC, Oostra BA, van Duijn CM, Hintzen RQ.
    J Hum Genet; 2009 Nov 15; 54(11):676-80. PubMed ID: 19834503
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  • 31. Gene-gene interaction between CD40 and CD40L reduces bone mineral density and increases osteoporosis risk in women.
    Pineda B, Tarín JJ, Hermenegildo C, Laporta P, Cano A, García-Pérez MÁ.
    Osteoporos Int; 2011 May 15; 22(5):1451-8. PubMed ID: 20577873
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  • 32. Risk alleles for multiple sclerosis identified by a genomewide study.
    International Multiple Sclerosis Genetics ConsortiumDivision of Molecular Immunology, Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, and Harvard Medical School, Boston, USA., Hafler DA, Compston A, Sawcer S, Lander ES, Daly MJ, De Jager PL, de Bakker PI, Gabriel SB, Mirel DB, Ivinson AJ, Pericak-Vance MA, Gregory SG, Rioux JD, McCauley JL, Haines JL, Barcellos LF, Cree B, Oksenberg JR, Hauser SL.
    N Engl J Med; 2007 Aug 30; 357(9):851-62. PubMed ID: 17660530
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  • 36. Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.
    Smets I, Fiddes B, Garcia-Perez JE, He D, Mallants K, Liao W, Dooley J, Wang G, Humblet-Baron S, Dubois B, Compston A, Jones J, Coles A, Liston A, Ban M, Goris A, Sawcer S.
    Brain; 2018 Mar 01; 141(3):786-796. PubMed ID: 29361022
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  • 37. Impact of CD40 gene polymorphisms on the risk of immune thrombocytopenic purpura.
    AbdelGhafar MT, El-Kholy RA, Elbedewy TA, Allam AA, Eissa RAE, Samy SM, El-Khalik SRA, Rabah H.
    Gene; 2020 Apr 30; 736():144419. PubMed ID: 32018016
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  • 38. Associations of CD6, TNFRSF1A and IRF8 polymorphisms with risk of inflammatory demyelinating diseases.
    Park TJ, Kim HJ, Kim JH, Bae JS, Cheong HS, Park BL, Shin HD.
    Neuropathol Appl Neurobiol; 2013 Aug 30; 39(5):519-30. PubMed ID: 22994200
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  • 39. Genetic variants in interleukin 7 receptor α chain (IL-7Ra) are associated with multiple sclerosis risk and disability progression in Central European Slovak population.
    Čierny D, Hányšová S, Michalik J, Kantorová E, Kurča E, Škereňová M, Lehotský J.
    J Neuroimmunol; 2015 May 15; 282():80-4. PubMed ID: 25903732
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  • 40. Interaction of Interleukin 7 Receptor (IL7R) and IL6 Gene Polymorphisms with Smoking Associated with Susceptibility to Asthma in Chinese Han Adults.
    Du JW, Xu ZL, Xu QX.
    Immunol Invest; 2022 Jul 15; 51(5):1364-1371. PubMed ID: 34236279
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