Kere J - Search Results

1

Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes.

Kaartokallio T, Lokki AI, Peterson H, Kivinen K, Hiltunen L, Salmela E, Lappalainen T, Maanselkä P, Heino S, Knuutila S, Sayed A, Poston L, Brennecke SP, Johnson MP, Morgan L, Moses EK, Kere J, Laivuori H. Kaartokallio T, et al. Among authors: kere j. Ann Med. 2016 Aug;48(5):330-6. doi: 10.1080/07853890.2016.1174877. Epub 2016 Apr 25. Ann Med. 2016. PMID: 27111527

2

Abnormalities of chromosomes 7 and 22 in human malignant pleural mesothelioma: correlation between Southern blot and cytogenetic analyses.

Tiainen M, Kere J, Tammilehto L, Mattson K, Knuutila S. Tiainen M, et al. Among authors: kere j. Genes Chromosomes Cancer. 1992 Mar;4(2):176-82. doi: 10.1002/gcc.2870040212. Genes Chromosomes Cancer. 1992. PMID: 1373319

3

Monocytic involvement by monosomy 7 preceded acute myelomonocytic leukemia in a patient with myelodysplastic syndrome.

Kere J, Knuutila S, Ruutu T, Leskinen R, de la Chapelle A. Kere J, et al. Leukemia. 1988 Feb;2(2):69-73. Leukemia. 1988. PMID: 3422700

4

Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.

Ignatius J, Knuutila S, Scherer SW, Trask B, Kere J. Ignatius J, et al. Among authors: kere j. J Med Genet. 1996 Jun;33(6):507-10. doi: 10.1136/jmg.33.6.507. J Med Genet. 1996. PMID: 8782053 Free PMC article.

5

Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm.

Kiuru-Kuhlefelt S, Kristo P, Ruutu T, Knuutila S, Kere J. Kiuru-Kuhlefelt S, et al. Among authors: kere j. Leukemia. 1997 Dec;11(12):2097-104. doi: 10.1038/sj.leu.2400881. Leukemia. 1997. PMID: 9447826

6

Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis.

Björkqvist AM, Wolf M, Nordling S, Tammilehto L, Knuuttila A, Kere J, Mattson K, Knuutila S. Björkqvist AM, et al. Among authors: kere j. Br J Cancer. 1999 Dec;81(7):1111-5. doi: 10.1038/sj.bjc.6690816. Br J Cancer. 1999. PMID: 10584869 Free PMC article. Clinical Trial.

7

Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans.

Kiuru-Kuhlefelt S, El-Rifai W, Fanburg-Smith J, Kere J, Miettinen M, Knuutila S. Kiuru-Kuhlefelt S, et al. Among authors: kere j. Cytogenet Cell Genet. 2001;92(3-4):192-5. doi: 10.1159/000056901. Cytogenet Cell Genet. 2001. PMID: 11435686

8

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.

9

Global analysis of uniparental disomy using high density genotyping arrays.

Bruce S, Leinonen R, Lindgren CM, Kivinen K, Dahlman-Wright K, Lipsanen-Nyman M, Hannula-Jouppi K, Kere J. Bruce S, et al. Among authors: kere j. J Med Genet. 2005 Nov;42(11):847-51. doi: 10.1136/jmg.2005.032367. Epub 2005 May 6. J Med Genet. 2005. PMID: 15879501 Free PMC 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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