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    VWA7 von Willebrand factor A domain containing 7 [ Homo sapiens (human) ]

    Gene ID: 80737, updated on 5-Mar-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    Observational study of gene-disease association. (HuGE Navigator)See all PubMed (4) articles

    Refining the association of MHC with multiple sclerosis in African Americans.
    McElroy JP, Cree BA, Caillier SJ, Gregersen PK, Herbert J, Khan OA, Freudenberg J, Lee A, Bridges SL Jr, Hauser SL, Oksenberg JR, Gourraud PA.

    High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.
    Barcellos LF, May SL, Ramsay PP, Quach HL, Lane JA, Nititham J, Noble JA, Taylor KE, Quach DL, Chung SA, Kelly JA, Moser KL, Behrens TW, Seldin MF, Thomson G, Harley JB, Gaffney PM, Criswell LA.

    Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease.
    Chapuis J, Hot D, Hansmannel F, Kerdraon O, Ferreira S, Hubans C, Maurage CA, Huot L, Bensemain F, Laumet G, Ayral AM, Fievet N, Hauw JJ, DeKosky ST, Lemoine Y, Iwatsubo T, Wavrant-Devrièze F, Dartigues JF, Tzourio C, Buée L, Pasquier F, Berr C, Mann D, Lendon C, Alpérovitch A, Kamboh MI, Amouyel P, Lambert JC.

    Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1.
    Valdes AM, Thomson G, Type 1 Diabetes Genetics Consortium.

    03/25/2009
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