Lie BA - Search Results

1

Maternal microchimerism in cord blood and risk of childhood-onset type 1 diabetes.

Tapia G, Mortimer G, Ye J, Gillard BT, Chipper-Keating S, Mårild K, Viken MK, Lie BA, Joner G, Skrivarhaug T, Njølstad PR, Størdal K, Gillespie KM, Stene LC. Tapia G, et al. Among authors: lie ba. Pediatr Diabetes. 2019 Sep;20(6):728-735. doi: 10.1111/pedi.12875. Epub 2019 Jun 19. Pediatr Diabetes. 2019. PMID: 31173445

2

HLA associations in insulin-dependent diabetes mellitus: no independent association to particular DP genes.

Lie BA, Akselsen HE, Joner G, Dahl-Jørgensen K, Rønningen KS, Thorsby E, Undlien DE. Lie BA, et al. Hum Immunol. 1997 Jul;55(2):170-5. doi: 10.1016/s0198-8859(97)00095-5. Hum Immunol. 1997. PMID: 9361969

3

The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene.

Lie BA, Todd JA, Pociot F, Nerup J, Akselsen HE, Joner G, Dahl-Jørgensen K, Rønningen KS, Thorsby E, Undlien DE. Lie BA, et al. Am J Hum Genet. 1999 Mar;64(3):793-800. doi: 10.1086/302283. Am J Hum Genet. 1999. PMID: 10053014 Free PMC article.

4

Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases.

Viken MK, Amundsen SS, Kvien TK, Boberg KM, Gilboe IM, Lilleby V, Sollid LM, Førre OT, Thorsby E, Smerdel A, Lie BA. Viken MK, et al. Among authors: lie ba. Genes Immun. 2005 May;6(3):271-3. doi: 10.1038/sj.gene.6364178. Genes Immun. 2005. PMID: 15759012

5

FOXP3 polymorphisms in type 1 diabetes and coeliac disease.

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. Bjørnvold M, et al. Among authors: lie ba. J Autoimmun. 2006 Sep;27(2):140-4. doi: 10.1016/j.jaut.2006.06.007. Epub 2006 Sep 20. J Autoimmun. 2006. PMID: 16996248

6

Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study.

Lie BA, Viken MK, Odegård S, van der Heijde D, Landewé R, Uhlig T, Kvien TK. Lie BA, et al. Ann Rheum Dis. 2007 Dec;66(12):1604-9. doi: 10.1136/ard.2006.067892. Epub 2007 May 1. Ann Rheum Dis. 2007. PMID: 17472988 Free PMC article.

7

Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease.

Lie BA, Viken MK, Akselsen HE, Flåm ST, Pociot F, Nerup J, Kockum I, Cambon-Thomsen A, Thorsby E, Undlien DE. Lie BA, et al. Hum Immunol. 2007 Jul;68(7):592-8. doi: 10.1016/j.humimm.2007.03.009. Epub 2007 Apr 13. Hum Immunol. 2007. PMID: 17584581

8

The PTPN22 promoter polymorphism -1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material.

Viken MK, Olsson M, Flåm ST, Førre O, Kvien TK, Thorsby E, Lie BA. Viken MK, et al. Among authors: lie ba. Tissue Antigens. 2007 Sep;70(3):190-7. doi: 10.1111/j.1399-0039.2007.00871.x. Tissue Antigens. 2007. PMID: 17661906

9

Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis.

Viken MK, Sollid HD, Joner G, Dahl-Jørgensen K, Rønningen KS, Undlien DE, Flatø B, Selvaag AM, Førre Ø, Kvien TK, Thorsby E, Melms A, Tolosa E, Lie BA. Viken MK, et al. Among authors: lie ba. Hum Immunol. 2007 Sep;68(9):748-55. doi: 10.1016/j.humimm.2007.05.009. Epub 2007 Jun 28. Hum Immunol. 2007. PMID: 17869649

10

The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases.

Eike MC, Nordang GB, Karlsen TH, Boberg KM, Vatn MH; IBSEN study group; Dahl-Jørgensen K, Rønningen KS, Joner G, Flatø B, Bergquist A, Thorsby E, Førre O, Kvien TK, Undlien DE, Lie BA. Eike MC, et al. Among authors: lie ba. Ann Rheum Dis. 2008 Sep;67(9):1287-91. doi: 10.1136/ard.2007.077826. Epub 2007 Dec 7. Ann Rheum Dis. 2008. PMID: 18065500

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