Kockum I - Search Results

1

A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis.

Mero IL, Lorentzen AR, Ban M, Smestad C, Celius EG, Aarseth JH, Myhr KM, Link J, Hillert J, Olsson T, Kockum I, Masterman T, Oturai AB, Søndergaard HB, Sellebjerg F, Saarela J, Kemppinen A, Elovaara I, Spurkland A, Dudbridge F, Lie BA, Harbo HF. Mero IL, et al. Among authors: kockum i. Eur J Hum Genet. 2010 Apr;18(4):502-4. doi: 10.1038/ejhg.2009.195. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888296 Free PMC article.

2

HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes.

Undlien DE, Kockum I, Rønningen KS, Lowe R, Saanjeevi CB, Graham J, Lie BA, Akselsen HE, Lernmark A, Thorsby E. Undlien DE, et al. Among authors: kockum i. Tissue Antigens. 1999 Dec;54(6):543-51. doi: 10.1034/j.1399-0039.1999.540602.x. Tissue Antigens. 1999. PMID: 10674967

3

Evidence of at least two type 1 diabetes susceptibility genes in the HLA complex distinct from HLA-DQB1, -DQA1 and -DRB1.

Johansson S, Lie BA, Todd JA, Pociot F, Nerup J, Cambon-Thomsen A, Kockum I, Akselsen HE, Thorsby E, Undlien DE. Johansson S, et al. Among authors: kockum i. Genes Immun. 2003 Jan;4(1):46-53. doi: 10.1038/sj.gene.6363917. Genes Immun. 2003. PMID: 12595901

4

HLA associations in type 1 diabetes: DPB1 alleles may act as markers of other HLA-complex susceptibility genes.

Johansson S, Lie BA, Pociot F, Nerup J, Cambon-Thomsen A, Kockum I, Thorsby E, Undlien DE. Johansson S, et al. Among authors: kockum i. Tissue Antigens. 2003 May;61(5):344-51. doi: 10.1034/j.1399-0039.2003.00055.x. Tissue Antigens. 2003. PMID: 12753653

5

No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex.

Johansson S, Lie BA, Cambon-Thomsen A, Pociot F, Nerup J, Kockum I, Thorsby E, Undlien DE. Johansson S, et al. Among authors: kockum i. Hum Immunol. 2003 Oct;64(10):951-9. doi: 10.1016/s0198-8859(03)00172-1. Hum Immunol. 2003. PMID: 14522092

6

Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB1*03 and DRB1*04 haplotypes.

Blomhoff A, Olsson M, Johansson S, Akselsen HE, Pociot F, Nerup J, Kockum I, Cambon-Thomsen A, Thorsby E, Undlien DE, Lie BA. Blomhoff A, et al. Among authors: kockum i. Genes Immun. 2006 Mar;7(2):130-40. doi: 10.1038/sj.gene.6364272. Genes Immun. 2006. PMID: 16395395

7

Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis.

Lundmark F, Duvefelt K, Iacobaeus E, Kockum I, Wallström E, Khademi M, Oturai A, Ryder LP, Saarela J, Harbo HF, Celius EG, Salter H, Olsson T, Hillert J. Lundmark F, et al. Among authors: kockum i. Nat Genet. 2007 Sep;39(9):1108-13. doi: 10.1038/ng2106. Epub 2007 Jul 29. Nat Genet. 2007. PMID: 17660816

8

The interleukin 23 receptor gene in multiple sclerosis: a case-control study.

Roos IM, Kockum I, Hillert J. Roos IM, et al. Among authors: kockum i. J Neuroimmunol. 2008 Feb;194(1-2):173-80. doi: 10.1016/j.jneuroim.2007.11.011. J Neuroimmunol. 2008. PMID: 18164077

9

Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families.

Ekelund E, Liedén A, Link J, Lee SP, D'Amato M, Palmer CN, Kockum I, Bradley M. Ekelund E, et al. Among authors: kockum i. Acta Derm Venereol. 2008;88(1):15-9. doi: 10.2340/00015555-0383. Acta Derm Venereol. 2008. PMID: 18176743 Free article.

10

Refining genetic associations in multiple sclerosis.

International Multiple Sclerosis Genetics Consortium (IMSGC). International Multiple Sclerosis Genetics Consortium (IMSGC). Lancet Neurol. 2008 Jul;7(7):567-9. doi: 10.1016/S1474-4422(08)70122-4. Lancet Neurol. 2008. PMID: 18565446 Free PMC article. No abstract available.

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