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Candidate gene region 15q26 and genetic susceptibility to coeliac disease in Finnish families.
Susi M, Holopainen P, Mustalahti K, Mäki M, Partanen J. Susi M, et al. Among authors: holopainen p. Scand J Gastroenterol. 2001 Apr;36(4):372-4. doi: 10.1080/003655201300051153. Scand J Gastroenterol. 2001. PMID: 11336161
Genetic polymorphism of the human ICOS gene.
Haimila KE, Partanen JA, Holopainen PM. Haimila KE, et al. Immunogenetics. 2002 Mar;53(12):1028-32. doi: 10.1007/s00251-002-0431-2. Epub 2002 Feb 6. Immunogenetics. 2002. PMID: 11904679
Technical note: linkage disequilibrium and disease-associated CTLA4 gene polymorphisms.
Holopainen PM, Partanen JA. Holopainen PM, et al. J Immunol. 2001 Sep 1;167(5):2457-8. doi: 10.4049/jimmunol.167.5.2457. J Immunol. 2001. PMID: 11509583
Candidate gene region 2q33 in European families with coeliac disease.
Holopainen P, Naluai AT, Moodie S, Percopo S, Coto I, Clot F, Ascher H, Sollid L, Ciclitira P, Greco L, Clerget-Darpoux F, Partanen J; Members of the European Genetics Cluster on Coeliac Disease. Holopainen P, et al. Tissue Antigens. 2004 Mar;63(3):212-22. doi: 10.1111/j.1399-0039.2004.00189.x. Tissue Antigens. 2004. PMID: 14989710
Genetic association of coeliac disease susceptibility to polymorphisms in the ICOS gene on chromosome 2q33.
Haimila K, Smedberg T, Mustalahti K, Mäki M, Partanen J, Holopainen P. Haimila K, et al. Among authors: holopainen p. Genes Immun. 2004 Mar;5(2):85-92. doi: 10.1038/sj.gene.6364040. Genes Immun. 2004. PMID: 14712308
CD80 (B7-1) and CD86 (B7-2) genes and genetic susceptibility to coeliac disease.
Woolley N, Holopainen P, Bourgain C, Mustalahti K, Collin P, Mäki M, Partanen J. Woolley N, et al. Among authors: holopainen p. Eur J Immunogenet. 2002 Aug;29(4):331-3. doi: 10.1046/j.1365-2370.2002.00302.x. Eur J Immunogenet. 2002. PMID: 12121279
Not all HLA DR3 DQ2 haplotypes confer equal susceptibility to coeliac disease: transmission analysis in families.
Karell K, Holopainen P, Mustalahti K, Collin P, Mäki M, Partanen J. Karell K, et al. Among authors: holopainen p. Scand J Gastroenterol. 2002 Jan;37(1):56-61. doi: 10.1080/003655202753387365. Scand J Gastroenterol. 2002. PMID: 11843036
Single founder mutation (W380G) in type II protein C deficiency in Finland.
Levo A, Kuismanen K, Holopainen P, Vahtera E, Rasi V, Holopainen P, Rasi V, Krusius T, Partanen J. Levo A, et al. Among authors: holopainen p. Thromb Haemost. 2000 Sep;84(3):424-8. Thromb Haemost. 2000. PMID: 11019966
CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study.
Holopainen P, Arvas M, Sistonen P, Mustalahti K, Collin P, Mäki M, Partanen J. Holopainen P, et al. Tissue Antigens. 1999 May;53(5):470-5. doi: 10.1034/j.1399-0039.1999.530503.x. Tissue Antigens. 1999. PMID: 10372542
Major histocompatibility complex (MHC)-linked microsatellite markers in a founder population.
Karell K, Klinger N, Holopainen P, Levo A, Partanen J. Karell K, et al. Among authors: holopainen p. Tissue Antigens. 2000 Jul;56(1):45-51. doi: 10.1034/j.1399-0039.2000.560106.x. Tissue Antigens. 2000. PMID: 10958355
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