Kere J - Search Results

1

Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.

Koskinen LL, Einarsdottir E, Korponay-Szabo IR, Kurppa K, Kaukinen K, Sistonen P, Pocsai Z, Széles G, Adány R, Mäki M, Kere J, Saavalainen P. Koskinen LL, et al. Among authors: kere j. Tissue Antigens. 2009 Nov;74(5):408-16. doi: 10.1111/j.1399-0039.2009.01359.x. Tissue Antigens. 2009. PMID: 19845895

2

Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.

Peltomäki P, Sistonen P, Mecklin JP, Pylkkänen L, Aaltonen L, Nordling S, Kere J, Järvinen H, Hamilton SR, Petersen G, et al. Peltomäki P, et al. Among authors: kere j. Cancer Res. 1992 Aug 15;52(16):4530-3. Cancer Res. 1992. PMID: 1643645

3

The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator.

Kere J, Sistonen P, Holmberg C, de la Chapelle A. Kere J, et al. Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10686-9. doi: 10.1073/pnas.90.22.10686. Proc Natl Acad Sci U S A. 1993. PMID: 7504277 Free PMC article.

4

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.

Höglund P, Sistonen P, Norio R, Holmberg C, Dimberg A, Gustavson KH, de la Chapelle A, Kere J. Höglund P, et al. Among authors: kere j. Am J Hum Genet. 1995 Jul;57(1):95-102. Am J Hum Genet. 1995. PMID: 7611301 Free PMC article.

5

[Linkage and linkage disequilibrium in the Finnish disease heritage].

de la Chapelle A, Hästbacka J, Lehesjoki AE, Sulisalo T, Kere J, Tahvanainen E, Sistonen P. de la Chapelle A, et al. Among authors: kere j. Duodecim. 1994;110(7):654-64. Duodecim. 1994. PMID: 8542820 Review. Finnish. No abstract available.

6

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: kere j. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

7

A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population.

Laitinen T, Daly MJ, Rioux JD, Kauppi P, Laprise C, Petäys T, Green T, Cargill M, Haahtela T, Lander ES, Laitinen LA, Hudson TJ, Kere J. Laitinen T, et al. Among authors: kere j. Nat Genet. 2001 May;28(1):87-91. doi: 10.1038/ng0501-87. Nat Genet. 2001. PMID: 11326283

8

A second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma.

Kauppi P, Lindblad-Toh K, Sevon P, Toivonen HT, Rioux JD, Villapakkam A, Laitinen LA, Hudson TJ, Kere J, Laitinen T. Kauppi P, et al. Among authors: kere j. Genomics. 2001 Sep;77(1-2):35-42. doi: 10.1006/geno.2001.6613. Genomics. 2001. PMID: 11543630

9

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.

Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J. Koillinen H, et al. Among authors: kere j. Eur J Hum Genet. 2001 Oct;9(10):747-52. doi: 10.1038/sj.ejhg.5200713. Eur J Hum Genet. 2001. PMID: 11781685

10

Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus.

Asumalahti K, Veal C, Laitinen T, Suomela S, Allen M, Elomaa O, Moser M, de Cid R, Ripatti S, Vorechovsky I, Marcusson JA, Nakagawa H, Lazaro C, Estivill X, Capon F, Novelli G, Saarialho-Kere U, Barker J, Trembath R, Kere J; Psoriasis Consortium. Asumalahti K, et al. Among authors: kere j. Hum Mol Genet. 2002 Mar 1;11(5):589-97. doi: 10.1093/hmg/11.5.589. Hum Mol Genet. 2002. PMID: 11875053

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