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Distinct molecular profiles in Lynch syndrome-associated and sporadic ovarian carcinomas.

Niskakoski A, Kaur S, Renkonen-Sinisalo L, Lassus H, Järvinen HJ, Mecklin JP, Bützow R, Peltomäki P. Niskakoski A, et al. Int J Cancer. 2013 Dec 1;133(11):2596-608. doi: 10.1002/ijc.28287. Epub 2013 Jun 21. Int J Cancer. 2013. PMID: 23716351

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Surveillance improves survival of colorectal cancer in patients with hereditary nonpolyposis colorectal cancer.

Renkonen-Sinisalo L, Aarnio M, Mecklin JP, Järvinen HJ. Renkonen-Sinisalo L, et al. Cancer Detect Prev. 2000;24(2):137-42. Cancer Detect Prev. 2000. PMID: 10917133

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No support for endoscopic surveillance for gastric cancer in hereditary non-polyposis colorectal cancer.

Renkonen-Sinisalo L, Sipponen P, Aarnio M, Julkunen R, Aaltonen LA, Sarna S, Järvinen HJ, Mecklin JP. Renkonen-Sinisalo L, et al. Scand J Gastroenterol. 2002 May;37(5):574-7. doi: 10.1080/00365520252903134. Scand J Gastroenterol. 2002. PMID: 12059060

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Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome.

Renkonen-Sinisalo L, Bützow R, Leminen A, Lehtovirta P, Mecklin JP, Järvinen HJ. Renkonen-Sinisalo L, et al. Int J Cancer. 2007 Feb 15;120(4):821-4. doi: 10.1002/ijc.22446. Int J Cancer. 2007. PMID: 17096354

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Utility of computed tomographic colonography in surveillance for hereditary nonpolyposis colorectal cancer syndrome.

Renkonen-Sinisalo L, Kivisaari A, Kivisaari L, Sarna S, Järvinen HJ. Renkonen-Sinisalo L, et al. Fam Cancer. 2007;6(1):135-40. doi: 10.1007/s10689-007-9116-1. Fam Cancer. 2007. PMID: 17273816

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Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds.

Grindedal EM, Renkonen-Sinisalo L, Vasen H, Evans G, Sala P, Blanco I, Gronwald J, Apold J, Eccles DM, Sánchez AA, Sampson J, Järvinen HJ, Bertario L, Crawford GC, Stormorken AT, Maehle L, Moller P. Grindedal EM, et al. J Med Genet. 2010 Feb;47(2):99-102. doi: 10.1136/jmg.2009.068130. Epub 2009 Jul 26. J Med Genet. 2010. PMID: 19635727

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Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members.

Järvinen HJ, Renkonen-Sinisalo L, Aktán-Collán K, Peltomäki P, Aaltonen LA, Mecklin JP. Järvinen HJ, et al. J Clin Oncol. 2009 Oct 1;27(28):4793-7. doi: 10.1200/JCO.2009.23.7784. Epub 2009 Aug 31. J Clin Oncol. 2009. PMID: 19720893

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Molecular analysis of endometrial tumorigenesis: importance of complex hyperplasia regardless of atypia.

Nieminen TT, Gylling A, Abdel-Rahman WM, Nuorva K, Aarnio M, Renkonen-Sinisalo L, Järvinen HJ, Mecklin JP, Bützow R, Peltomäki P. Nieminen TT, et al. Clin Cancer Res. 2009 Sep 15;15(18):5772-83. doi: 10.1158/1078-0432.CCR-09-0506. Epub 2009 Sep 1. Clin Cancer Res. 2009. PMID: 19723644

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Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.

Vasen HF, Möslein G, Alonso A, Aretz S, Bernstein I, Bertario L, Blanco I, Bulow S, Burn J, Capella G, Colas C, Engel C, Frayling I, Rahner N, Hes FJ, Hodgson S, Mecklin JP, Møller P, Myrhøj T, Nagengast FM, Parc Y, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen J, Lubinski J, Järvinen H, Claes E, Heinimann K, Karagiannis JA, Lindblom A, Dove-Edwin I, Müller H. Vasen HF, et al. Fam Cancer. 2010 Jun;9(2):109-15. doi: 10.1007/s10689-009-9291-3. Epub 2009 Sep 18. Fam Cancer. 2010. PMID: 19763885

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Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.

Vasen HF, Blanco I, Aktan-Collan K, Gopie JP, Alonso A, Aretz S, Bernstein I, Bertario L, Burn J, Capella G, Colas C, Engel C, Frayling IM, Genuardi M, Heinimann K, Hes FJ, Hodgson SV, Karagiannis JA, Lalloo F, Lindblom A, Mecklin JP, Møller P, Myrhoj T, Nagengast FM, Parc Y, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Sijmons RH, Tejpar S, Thomas HJ, Rahner N, Wijnen JT, Järvinen HJ, Möslein G; Mallorca group. Vasen HF, et al. Gut. 2013 Jun;62(6):812-23. doi: 10.1136/gutjnl-2012-304356. Epub 2013 Feb 13. Gut. 2013. PMID: 23408351 Free PMC article.

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