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181 related items for PubMed ID: 20506482

  • 1. Assessment of complement C4 gene copy number using the paralog ratio test.
    Fernando MM, Boteva L, Morris DL, Zhou B, Wu YL, Lokki ML, Yu CY, Rioux JD, Hollox EJ, Vyse TJ.
    Hum Mutat; 2010 Jul; 31(7):866-74. PubMed ID: 20506482
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  • 2. Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans.
    Yang Y, Chung EK, Wu YL, Savelli SL, Nagaraja HN, Zhou B, Hebert M, Jones KN, Shu Y, Kitzmiller K, Blanchong CA, McBride KL, Higgins GC, Rennebohm RM, Rice RR, Hackshaw KV, Roubey RA, Grossman JM, Tsao BP, Birmingham DJ, Rovin BH, Hebert LA, Yu CY.
    Am J Hum Genet; 2007 Jun; 80(6):1037-54. PubMed ID: 17503323
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  • 9. Association between complement 4 copy number variation and systemic lupus erythematosus: a meta-analysis.
    Wu Z, Zhang S, Li P, Zhang F, Li Y.
    Clin Exp Med; 2020 Nov; 20(4):627-634. PubMed ID: 32691186
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  • 10. Insights on the relationship between complement component C4 serum concentrations and C4 gene copy numbers in a Western Australian systemic lupus erythematosus cohort.
    Margery-Muir AA, Bundell C, Wetherall JD, Whidborne R, Martinez P, Groth DM.
    Lupus; 2018 Sep; 27(10):1687-1696. PubMed ID: 30041577
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  • 11. A rare complement component C4 restriction fragment length polymorphism in two families with systemic lupus erythematosus.
    Goldstein R, Moulds JM, Sengar DP.
    J Rheumatol; 1991 Mar; 18(3):345-8. PubMed ID: 1677422
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  • 13. Establishment of gene copy number-specific normal ranges for serum C4 and its utility for interpretation in patients with chronically low serum C4 concentrations.
    Margery-Muir AA, Wetherall JD, Castley AS, Hew M, Whidborne RS, Mallon DF, Martinez P, Witt CS.
    Arthritis Rheumatol; 2014 Sep; 66(9):2512-20. PubMed ID: 24757030
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  • 14. Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus.
    Wu YL, Yang Y, Chung EK, Zhou B, Kitzmiller KJ, Savelli SL, Nagaraja HN, Birmingham DJ, Tsao BP, Rovin BH, Hebert LA, Yu CY.
    Cytogenet Genome Res; 2008 Sep; 123(1-4):131-41. PubMed ID: 19287147
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  • 15. Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.
    Saxena K, Kitzmiller KJ, Wu YL, Zhou B, Esack N, Hiremath L, Chung EK, Yang Y, Yu CY.
    Mol Immunol; 2009 Apr; 46(7):1289-303. PubMed ID: 19135723
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  • 16. Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.
    Chen JY, Wu YL, Mok MY, Wu YJ, Lintner KE, Wang CM, Chung EK, Yang Y, Zhou B, Wang H, Yu D, Alhomosh A, Jones K, Spencer CH, Nagaraja HN, Lau YL, Lau CS, Yu CY.
    Arthritis Rheumatol; 2016 Jun; 68(6):1442-1453. PubMed ID: 26814708
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  • 17. Deficiency of C4A is a genetic determinant of systemic lupus erythematosus in three ethnic groups.
    Dunckley H, Gatenby PA, Hawkins B, Naito S, Serjeantson SW.
    J Immunogenet; 1987 Jun; 14(4-5):209-18. PubMed ID: 3502648
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  • 19. The intricate role of complement component C4 in human systemic lupus erythematosus.
    Yang Y, Chung EK, Zhou B, Lhotta K, Hebert LA, Birmingham DJ, Rovin BH, Yu CY.
    Curr Dir Autoimmun; 2004 Jun; 7():98-132. PubMed ID: 14719377
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  • 20. Complement genes contribute sex-biased vulnerability in diverse disorders.
    Kamitaki N, Sekar A, Handsaker RE, de Rivera H, Tooley K, Morris DL, Taylor KE, Whelan CW, Tombleson P, Loohuis LMO, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Boehnke M, Kimberly RP, Kaufman KM, Harley JB, Langefeld CD, Seidman CE, Pato MT, Pato CN, Ophoff RA, Graham RR, Criswell LA, Vyse TJ, McCarroll SA.
    Nature; 2020 Jun; 582(7813):577-581. PubMed ID: 32499649
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