Ollila S - Search Results

1

Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.

Ollila S, Sarantaus L, Kariola R, Chan P, Hampel H, Holinski-Feder E, Macrae F, Kohonen-Corish M, Gerdes AM, Peltomäki P, Mangold E, de la Chapelle A, Greenblatt M, Nyström M. Ollila S, et al. Gastroenterology. 2006 Nov;131(5):1408-17. doi: 10.1053/j.gastro.2006.08.044. Epub 2006 Aug 22. Gastroenterology. 2006. PMID: 17101317

2

The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC.

Ollila S, Fitzpatrick R, Sarantaus L, Kariola R, Ambus I, Velsher L, Hsieh E, Andersen MK, Raevaara TE, Gerdes AM, Mangold E, Peltomäki P, Lynch HT, Nyström M. Ollila S, et al. Int J Oncol. 2006 Jan;28(1):149-53. Int J Oncol. 2006. PMID: 16327991

3

Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.

Zhang J, Lindroos A, Ollila S, Russell A, Marra G, Mueller H, Peltomaki P, Plasilova M, Heinimann K. Zhang J, et al. Among authors: ollila s. Cancer Res. 2006 Jan 15;66(2):659-64. doi: 10.1158/0008-5472.CAN-05-4043. Cancer Res. 2006. PMID: 16423994 Free article.

4

Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR).

Chan PA, Duraisamy S, Miller PJ, Newell JA, McBride C, Bond JP, Raevaara T, Ollila S, Nyström M, Grimm AJ, Christodoulou J, Oetting WS, Greenblatt MS. Chan PA, et al. Among authors: ollila s. Hum Mutat. 2007 Jul;28(7):683-93. doi: 10.1002/humu.20492. Hum Mutat. 2007. PMID: 17370310

5

Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification.

Ollila S, Dermadi Bebek D, Greenblatt M, Nyström M. Ollila S, et al. Int J Cancer. 2008 Aug 1;123(3):720-4. doi: 10.1002/ijc.23573. Int J Cancer. 2008. PMID: 18470917

6

Mechanisms of pathogenicity in human MSH2 missense mutants.

Ollila S, Dermadi Bebek D, Jiricny J, Nyström M. Ollila S, et al. Hum Mutat. 2008 Nov;29(11):1355-63. doi: 10.1002/humu.20893. Hum Mutat. 2008. PMID: 18951462

7

Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome.

Gargiulo S, Torrini M, Ollila S, Nasti S, Pastorino L, Cusano R, Bonelli L, Battistuzzi L, Mastracci L, Bruno W, Savarino V, Sciallero S, Borgonovo G, Nyström M, Bianchi-Scarrà G, Mareni C, Ghiorzo P. Gargiulo S, et al. Among authors: ollila s. Fam Cancer. 2009;8(4):547-53. doi: 10.1007/s10689-009-9285-1. Fam Cancer. 2009. PMID: 19728162

8

MutSbeta exceeds MutSalpha in dinucleotide loop repair.

Kantelinen J, Kansikas M, Korhonen MK, Ollila S, Heinimann K, Kariola R, Nyström M. Kantelinen J, et al. Among authors: ollila s. Br J Cancer. 2010 Mar 16;102(6):1068-73. doi: 10.1038/sj.bjc.6605531. Epub 2010 Feb 16. Br J Cancer. 2010. PMID: 20160730 Free PMC article.

9

A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one.

Kantelinen J, Hansen TV, Kansikas M, Krogh LN, Korhonen MK, Ollila S, Nyström M, Gerdes AM, Kariola R. Kantelinen J, et al. Among authors: ollila s. Fam Cancer. 2011 Sep;10(3):515-20. doi: 10.1007/s10689-011-9436-z. Fam Cancer. 2011. PMID: 21431882

10

Cancer-predicting gene expression changes in colonic mucosa of Western diet fed Mlh1+/- mice.

Pussila M, Sarantaus L, Dermadi Bebek D, Valo S, Reyhani N, Ollila S, Päivärinta E, Peltomäki P, Mutanen M, Nyström M. Pussila M, et al. Among authors: ollila s. PLoS One. 2013 Oct 8;8(10):e76865. doi: 10.1371/journal.pone.0076865. eCollection 2013. PLoS One. 2013. PMID: 24204690 Free PMC article.

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