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Items: 1 to 20 of 92

1.

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.

Ferreira RC, Pan-Hammarström Q, Graham RR, Gateva V, Fontán G, Lee AT, Ortmann W, Urcelay E, Fernández-Arquero M, Núñez C, Jorgensen G, Ludviksson BR, Koskinen S, Haimila K, Clark HF, Klareskog L, Gregersen PK, Behrens TW, Hammarström L.

Nat Genet. 2010 Sep;42(9):777-80. doi: 10.1038/ng.644. Epub 2010 Aug 8.

PMID:
20694011
2.

Association of immunoglobulin A deficiency and elevated thyrotropin-receptor autoantibodies in two Nordic countries.

Jorgensen GH, Ornolfsson AE, Johannesson A, Gudmundsson S, Janzi M, Wang N, Hammarström L, Ludviksson BR.

Hum Immunol. 2011 Feb;72(2):166-72. doi: 10.1016/j.humimm.2010.10.014. Epub 2010 Oct 25.

PMID:
20977916
4.

High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency.

Ferreira RC, Pan-Hammarström Q, Graham RR, Fontán G, Lee AT, Ortmann W, Wang N, Urcelay E, Fernández-Arquero M, Núñez C, Jorgensen G, Ludviksson BR, Koskinen S, Haimila K, Padyukov L, Gregersen PK, Hammarström L, Behrens TW.

PLoS Genet. 2012 Jan;8(1):e1002476. doi: 10.1371/journal.pgen.1002476. Epub 2012 Jan 26.

5.

Selective IgA deficiency in autoimmune diseases.

Wang N, Shen N, Vyse TJ, Anand V, Gunnarson I, Sturfelt G, Rantapää-Dahlqvist S, Elvin K, Truedsson L, Andersson BA, Dahle C, Ortqvist E, Gregersen PK, Behrens TW, Hammarström L.

Mol Med. 2011;17(11-12):1383-96. doi: 10.2119/molmed.2011.00195. Epub 2011 Aug 4. Review.

6.
7.

Genetics: Rare genes for autoimmunity-the new kids on the block.

Satterthwaite AB, Mohan C.

Nat Rev Rheumatol. 2010 Dec;6(12):678-9. doi: 10.1038/nrrheum.2010.177. No abstract available.

8.

Carriers of rare missense variants in IFIH1 are protected from psoriasis.

Li Y, Liao W, Cargill M, Chang M, Matsunami N, Feng BJ, Poon A, Callis-Duffin KP, Catanese JJ, Bowcock AM, Leppert MF, Kwok PY, Krueger GG, Begovich AB.

J Invest Dermatol. 2010 Dec;130(12):2768-72. doi: 10.1038/jid.2010.214. Epub 2010 Jul 29.

9.

Human leukocyte antigens (HLA) associated with selective IgA deficiency in Iran and Sweden.

Mohammadi J, Pourpak Z, Jarefors S, Saghafi S, Zendehdel K, Pourfathollah AA, Amirzargar AA, Aghamohammadi A, Moin M, Hammarstrom L.

Iran J Allergy Asthma Immunol. 2008 Dec;7(4):209-14. doi: 07.04/ijaai.209214.

10.

Brief Report: IFIH1 Mutation Causes Systemic Lupus Erythematosus With Selective IgA Deficiency.

Van Eyck L, De Somer L, Pombal D, Bornschein S, Frans G, Humblet-Baron S, Moens L, de Zegher F, Bossuyt X, Wouters C, Liston A.

Arthritis Rheumatol. 2015 Jun;67(6):1592-7. doi: 10.1002/art.39110.

11.

Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.

Bronson PG, Chang D, Bhangale T, Seldin MF, Ortmann W, Ferreira RC, Urcelay E, Pereira LF, Martin J, Plebani A, Lougaris V, Friman V, Freiberger T, Litzman J, Thon V, Pan-Hammarström Q, Hammarström L, Graham RR, Behrens TW.

Nat Genet. 2016 Nov;48(11):1425-1429. doi: 10.1038/ng.3675. Epub 2016 Oct 10.

12.

Association of IFIH1 rs1990760 polymorphism with susceptibility to autoimmune diseases: a meta-analysis.

Cen H, Wang W, Leng RX, Wang TY, Pan HF, Fan YG, Wang B, Ye DQ.

Autoimmunity. 2013 Nov;46(7):455-62. doi: 10.3109/08916934.2013.796937. Epub 2013 Jun 4. Review.

PMID:
23734776
13.

IgA deficiency: what is new?

Wang N, Hammarström L.

Curr Opin Allergy Clin Immunol. 2012 Dec;12(6):602-8. doi: 10.1097/ACI.0b013e3283594219. Review.

PMID:
23026772
14.

Interferon induced with helicase C domain 1 (IFIH1) and virus-induced autoimmunity: a review.

Chistiakov DA.

Viral Immunol. 2010 Feb;23(1):3-15. doi: 10.1089/vim.2009.0071. Review.

PMID:
20121398
15.

Polymorphisms in the innate immune IFIH1 gene, frequency of enterovirus in monthly fecal samples during infancy, and islet autoimmunity.

Witsø E, Tapia G, Cinek O, Pociot FM, Stene LC, Rønningen KS.

PLoS One. 2011;6(11):e27781. doi: 10.1371/journal.pone.0027781. Epub 2011 Nov 14.

16.

Familial aggregation of IgAD and autoimmunity.

Jorgensen GH, Thorsteinsdottir I, Gudmundsson S, Hammarstrom L, Ludviksson BR.

Clin Immunol. 2009 May;131(2):233-9. doi: 10.1016/j.clim.2008.11.013. Epub 2009 Jan 24.

PMID:
19167929
17.

An interferon-induced helicase (IFIH1) gene polymorphism associates with different rates of progression from autoimmunity to type 1 diabetes.

Winkler C, Lauber C, Adler K, Grallert H, Illig T, Ziegler AG, Bonifacio E.

Diabetes. 2011 Feb;60(2):685-90. doi: 10.2337/db10-1269.

18.

Cumulative effect of IFIH1 variants and increased gene expression associated with type 1 diabetes.

Zurawek M, Fichna M, Fichna P, Skowronska B, Dzikiewicz-Krawczyk A, Januszkiewicz D, Nowak J.

Diabetes Res Clin Pract. 2015 Feb;107(2):259-66. doi: 10.1016/j.diabres.2014.11.008. Epub 2014 Dec 4.

PMID:
25515714
19.

Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production.

Molineros JE, Maiti AK, Sun C, Looger LL, Han S, Kim-Howard X, Glenn S, Adler A, Kelly JA, Niewold TB, Gilkeson GS, Brown EE, Alarcón GS, Edberg JC, Petri M, Ramsey-Goldman R, Reveille JD, Vilá LM, Freedman BI, Tsao BP, Criswell LA, Jacob CO, Moore JH, Vyse TJ, Langefeld CL, Guthridge JM, Gaffney PM, Moser KL, Scofield RH, Alarcón-Riquelme ME; BIOLUPUS Network, Williams SM, Merrill JT, James JA, Kaufman KM, Kimberly RP, Harley JB, Nath SK.

PLoS Genet. 2013;9(2):e1003222. doi: 10.1371/journal.pgen.1003222. Epub 2013 Feb 18.

20.

Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.

Sutherland A, Davies J, Owen CJ, Vaikkakara S, Walker C, Cheetham TD, James RA, Perros P, Donaldson PT, Cordell HJ, Quinton R, Pearce SH.

J Clin Endocrinol Metab. 2007 Aug;92(8):3338-41. Epub 2007 May 29.

PMID:
17535987

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