Kere J - Search Results

1

Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.

Salmela E, Lappalainen T, Liu J, Sistonen P, Andersen PM, Schreiber S, Savontaus ML, Czene K, Lahermo P, Hall P, Kere J. Salmela E, et al. Among authors: kere j. PLoS One. 2011 Feb 9;6(2):e16747. doi: 10.1371/journal.pone.0016747. PLoS One. 2011. PMID: 21347369 Free PMC article.

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

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

6

A novel low-penetrance locus for familial glioma at 15q23-q26.3.

Paunu N, Lahermo P, Onkamo P, Ollikainen V, Rantala I, Helén P, Simola KO, Kere J, Haapasalo H. Paunu N, et al. Among authors: kere j. Cancer Res. 2002 Jul 1;62(13):3798-802. Cancer Res. 2002. PMID: 12097292

7

Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.

Laivuori H, Lahermo P, Ollikainen V, Widen E, Häivä-Mällinen L, Sundström H, Laitinen T, Kaaja R, Ylikorkala O, Kere J. Laivuori H, et al. Among authors: kere j. Am J Hum Genet. 2003 Jan;72(1):168-77. doi: 10.1086/345311. Epub 2002 Dec 9. Am J Hum Genet. 2003. PMID: 12474145 Free PMC article.

8

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.

Kaminen N, Hannula-Jouppi K, Kestilä M, Lahermo P, Muller K, Kaaranen M, Myllyluoma B, Voutilainen A, Lyytinen H, Nopola-Hemmi J, Kere J. Kaminen N, et al. Among authors: kere j. J Med Genet. 2003 May;40(5):340-5. doi: 10.1136/jmg.40.5.340. J Med Genet. 2003. PMID: 12746395 Free PMC article.

9

Psoriasis susceptibility locus on 18p revealed by genome scan in Finnish families not associated with PSORS1.

Asumalahti K, Laitinen T, Lahermo P, Suomela S, Itkonen-Vatjus R, Jansen C, Karvonen J, Karvonen SL, Reunala T, Snellman E, Uurasmaa T, Saarialho-Kere U, Kere J. Asumalahti K, et al. Among authors: kere j. J Invest Dermatol. 2003 Oct;121(4):735-40. doi: 10.1046/j.1523-1747.2003.12483.x. J Invest Dermatol. 2003. PMID: 14632189 Free article.

10

Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.

Salmela E, Taskinen O, Seppänen JK, Sistonen P, Daly MJ, Lahermo P, Savontaus ML, Kere J. Salmela E, et al. Among authors: kere j. J Med Genet. 2006 Jul;43(7):590-7. doi: 10.1136/jmg.2005.038414. Epub 2006 Jan 27. J Med Genet. 2006. PMID: 16443857 Free PMC article.

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