Torniainen S - Search Results

1

Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD).

Torniainen S, Freddara R, Routi T, Gijsbers C, Catassi C, Höglund P, Savilahti E, Järvelä I. Torniainen S, et al. BMC Gastroenterol. 2009 Jan 22;9:8. doi: 10.1186/1471-230X-9-8. BMC Gastroenterol. 2009. PMID: 19161632 Free PMC article.

2

[Congenital lactase deficiency--a more common disease than previously thought?].

Torniainen S, Savilahti E, Järvelä I. Torniainen S, et al. Duodecim. 2009;125(7):766-70. Duodecim. 2009. PMID: 19432082 Finnish.

3

Screening of variants for lactase persistence/non-persistence in populations from South Africa and Ghana.

Torniainen S, Parker MI, Holmberg V, Lahtela E, Dandara C, Jarvela I. Torniainen S, et al. BMC Genet. 2009 Jul 5;10:31. doi: 10.1186/1471-2156-10-31. BMC Genet. 2009. PMID: 19575818 Free PMC article.

4

Molecular genetics of human lactase deficiencies.

Järvelä I, Torniainen S, Kolho KL. Järvelä I, et al. Among authors: torniainen s. Ann Med. 2009;41(8):568-75. doi: 10.1080/07853890903121033. Ann Med. 2009. PMID: 19639477 Review.

5

Lactase persistence, dietary intake of milk, and the risk for prostate cancer in Sweden and Finland.

Torniainen S, Hedelin M, Autio V, Rasinperä H, Bälter KA, Klint A, Bellocco R, Wiklund F, Stattin P, Ikonen T, Tammela TL, Schleutker J, Grönberg H, Järvelä I. Torniainen S, et al. Cancer Epidemiol Biomarkers Prev. 2007 May;16(5):956-61. doi: 10.1158/1055-9965.EPI-06-0985. Cancer Epidemiol Biomarkers Prev. 2007. PMID: 17507622

6

The -13914G>A variant upstream of the lactase gene (LCT) is associated with lactase persistence/non-persistence.

Khabarova Y, Torniainen S, Savilahti E, Isokoski M, Mattila K, Järvelä I. Khabarova Y, et al. Among authors: torniainen s. Scand J Clin Lab Invest. 2010 Sep;70(5):354-7. doi: 10.3109/00365513.2010.491554. Scand J Clin Lab Invest. 2010. PMID: 20509822

7

Lactase non-persistence and milk consumption in Estonia.

Lember M, Torniainen S, Kull M, Kallikorm R, Saadla P, Rajasalu T, Komu H, Järvelä I. Lember M, et al. Among authors: torniainen s. World J Gastroenterol. 2006 Dec 7;12(45):7329-31. doi: 10.3748/wjg.v12.i45.7329. World J Gastroenterol. 2006. PMID: 17143950 Free PMC article.

8

Screening of DNA-variants in the properdin gene (CFP) in age-related macular degeneration (AMD).

Seitsonen S, Onkamo P, Torniainen S, Ihalainen M, Immonen I, Meri S, Järvelä I. Seitsonen S, et al. Among authors: torniainen s. Mol Immunol. 2010 Mar;47(6):1334-6. doi: 10.1016/j.molimm.2010.01.001. Epub 2010 Jan 31. Mol Immunol. 2010. PMID: 20122735

9

Novel PORCN mutations in focal dermal hypoplasia.

Froyen G, Govaerts K, Van Esch H, Verbeeck J, Tuomi ML, Heikkilä H, Torniainen S, Devriendt K, Fryns JP, Marynen P, Järvelä I, Ala-Mello S. Froyen G, et al. Among authors: torniainen s. Clin Genet. 2009 Dec;76(6):535-43. doi: 10.1111/j.1399-0004.2009.01248.x. Epub 2009 Oct 23. Clin Genet. 2009. PMID: 19863546

10

Prevalence of lactase persistent/non-persistent genotypes and milk consumption in a young population in north-west Russia.

Khabarova Y, Torniainen ST, Nurmi HA, Järvelä IE, Isokoski MK, Mattila KJ. Khabarova Y, et al. Among authors: torniainen st. World J Gastroenterol. 2009 Apr 21;15(15):1849-53. doi: 10.3748/wjg.15.1849. World J Gastroenterol. 2009. PMID: 19370782 Free PMC article.

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