Beate Skinningsrud

     

    Author network for Beate Skinningsrud by COREMINE medical


    Publications 2015

    Wolff AS, Mitchell AL, Cordell HJ, Short A, Skinningsrud B, Ollier W, Badenhoop K, Meyer G, Falorni A, Kampe O, Undlien D, Pearce SH, Husebye ES (2015)
    CTLA-4 as a genetic determinant in autoimmune Addison's disease
    Genes Immun, 16 (6), 430-6
    DOI 10.1038/gene.2015.27, PubMed 26204230

    Publications 2014

    Brønstad I, Skinningsrud B, Bratland E, Løvås K, Undlien D, Sverre Husebye E, Wolff AS (2014)
    CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles
    Eur J Endocrinol, 171 (6), 743-50
    DOI 10.1530/EJE-14-0432, PubMed 25249698

    Mitchell AL, Macarthur KD, Gan EH, Baggott LE, Wolff AS, Skinningsrud B, Platt H, Short A, Lobell A, Kämpe O, Bensing S, Betterle C, Kasperlik-Zaluska A, Zurawek M, Fichna M, Kockum I, Nordling Eriksson G, Ekwall O, Wahlberg J, Dahlqvist P, Hulting AL, Penna-Martinez M, Meyer G, Kahles H, Badenhoop K et al. (2014)
    Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts
    PLoS One, 9 (3), e88991
    DOI 10.1371/journal.pone.0088991, PubMed 24614117

    Publications 2012

    Eike MC, Skinningsrud B, Ronninger M, Stormyr A, Kvien TK, Joner G, Njølstad PR, Førre O, Flatø B, Alfredsson L, Padyukov L, Undlien DE, Lie BA (2012)
    CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations
    Genes Immun, 13 (5), 431-6
    DOI 10.1038/gene.2012.11, PubMed 22513452

    Ronninger M, Seddighzadeh M, Eike MC, Plant D, Daha NA, Skinningsrud B, Worthington J, Kvien TK, Toes RE, Lie BA, Alfredsson L, Padyukov L (2012)
    Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis
    PLoS One, 7 (3), e32861
    DOI 10.1371/journal.pone.0032861, PubMed 22461888

    Publications 2011

    Skinningsrud B, Lie BA, Lavant E, Carlson JA, Erlich H, Akselsen HE, Gervin K, Wolff AB, Erichsen MM, Løvås K, Husebye ES, Undlien DE (2011)
    Multiple loci in the HLA complex are associated with Addison's disease
    J Clin Endocrinol Metab, 96 (10), E1703-8
    DOI 10.1210/jc.2011-0645, PubMed 21816777

    Publications 2010

    Mero IL, Ban M, Lorentzen ÅR, Smestad C, Celius EG, Sæther H, Saeedi H, Viken MK, Skinningsrud B, Undlien DE, Aarseth J, Myhr KM, Granum S, Spurkland A, Sawcer S, Compston A, Lie BA, Harbo HF (2010)
    Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
    Genes Immun, 12 (3), 191-8
    DOI 10.1038/gene.2010.59, PubMed 21179112

    Publications 2009

    Bratland E, Skinningsrud B, Undlien DE, Mozes E, Husebye ES (2009)
    T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency
    J Clin Endocrinol Metab, 94 (12), 5117-24
    DOI 10.1210/jc.2009-1115, PubMed 19890026

    Erichsen MM, Løvås K, Skinningsrud B, Wolff AB, Undlien DE, Svartberg J, Fougner KJ, Berg TJ, Bollerslev J, Mella B, Carlson JA, Erlich H, Husebye ES (2009)
    Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry
    J Clin Endocrinol Metab, 94 (12), 4882-90
    DOI 10.1210/jc.2009-1368, PubMed 19858318

    Mitchell AL, Cordell HJ, Soemedi R, Owen K, Skinningsrud B, Wolff AB, Ericksen M, Undlien D, Husebye E, Pearce SH (2009)
    Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility
    J Clin Endocrinol Metab, 94 (12), 5139-45
    DOI 10.1210/jc.2009-1404, PubMed 19850680

    Skinningsrud B, Husebye ES, Gilfillan GD, Frengen E, Erichsen A, Gervin K, Ormerod E, Egeland T, Undlien DE (2009)
    X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene
    J Clin Endocrinol Metab, 94 (10), 4086-93
    DOI 10.1210/jc.2009-0923, PubMed 19773398

    Skinningsrud B, Lie BA, Husebye ES, Kvien TK, Førre Ø, Flatø B, Stormyr A, Joner G, Njølstad PR, Egeland T, Undlien DE (2009)
    A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis
    Ann Rheum Dis, 69 (8), 1471-4
    DOI 10.1136/ard.2009.114934, PubMed 19734133

    Publications 2008

    Magitta NF, Bøe Wolff AS, Johansson S, Skinningsrud B, Lie BA, Myhr KM, Undlien DE, Joner G, Njølstad PR, Kvien TK, Førre Ø, Knappskog PM, Husebye ES (2008)
    A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
    Genes Immun, 10 (2), 120-4
    DOI 10.1038/gene.2008.85, PubMed 18946481

    Skinningsrud B, Husebye ES, Gervin K, Løvås K, Blomhoff A, Wolff AB, Kemp EH, Egeland T, Undlien DE (2008)
    Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease
    Eur J Hum Genet, 16 (8), 977-82
    DOI 10.1038/ejhg.2008.33, PubMed 18301444

    Skinningsrud B, Husebye ES, Pearce SH, McDonald DO, Brandal K, Wolff AB, Løvås K, Egeland T, Undlien DE (2008)
    Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency
    J Clin Endocrinol Metab, 93 (9), 3310-7
    DOI 10.1210/jc.2008-0821, PubMed 18593762

    Publications 2007

    Munthe-Kaas MC, Gerritsen J, Carlsen KH, Undlien D, Egeland T, Skinningsrud B, Tørres T, Carlsen KL (2007)
    Eosinophil cationic protein (ECP) polymorphisms and association with asthma, s-ECP levels and related phenotypes
    Allergy, 62 (4), 429-36
    DOI 10.1111/j.1398-9995.2007.01327.x, PubMed 17362255

    Publications 2006

    Bjørnvold M, Amundsen SS, Stene LC, Joner G, Dahl-Jørgensen K, Njølstad PR, Ek J, Ascher H, Gudjònsdòttir AH, Lie BA, Skinningsrud B, Akselsen HE, Rønningen KS, Sollid LM, Undlien DE (2006)
    FOXP3 polymorphisms in type 1 diabetes and coeliac disease
    J Autoimmun, 27 (2), 140-4
    DOI 10.1016/j.jaut.2006.06.007, PubMed 16996248

    Munthe-Kaas MC, Lødrup Carlsen KC, Carlsen KH, Skinningsrud B, Håland G, Devulapalli CS, Pettersen M, Eiklid K (2006)
    CFTR gene mutations and asthma in the Norwegian Environment and Childhood Asthma study
    Respir Med, 100 (12), 2121-8
    DOI 10.1016/j.rmed.2006.03.026, PubMed 16678395

    Publications 2004

    Munthe-Kaas MC, Carlsen KH, Helms PJ, Gerritsen J, Whyte M, Feijen M, Skinningsrud B, Main M, Kwong GN, Lie BA, Lødrup Carlsen KC, Undlien DE (2004)
    CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigm
    J Allergy Clin Immunol, 114 (2), 280-7
    DOI 10.1016/j.jaci.2004.03.050, PubMed 15316504

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