Hereditary Colorectal Cancer

Paper I: Journal of Clinical Oncology 19(20), Vasen, H. F. A.; Stormorken, A.; Menko, F. H.; Nagengast, F. M.; Kleibeuker, J. H.; Griffioen, G.; Taal, B. G.; Moller, P. and J.T. Wijnen, MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers. A study of 138 HNPCC families, pp. 4074-4080. Copyright © 2001 by the American Society of Clinical Oncology.

Paper II: Gastroenterology 127, Hendriks, Yvonne M. C.; Wagner, Anja; Morreau, Hans; Menko, Fred; Stormorken, Astrid; Quehenberger, Franz; Sandkuijl, Lodewijk; Møller, Pal; Genuardi, Maurizio; Houwelingen, Hans van; Tops, Carli; Puijenbroek, Marjo van; Verkuijlen, Paul; Kenter, Gemma; Mil, Anneke van; Meijers-Heijboer, Hanne; Tan, Gita B.; Breuning, Martijn H.; Fodde, Riccardo; Winjen, Jull Th.; Bröcker–Vriends, Annette H. J. T. and Hans Vasen, Cancer risk in Hereditary nonpolyposis colorectal caner due to MSH6 mutations: Impact on counseling and surveillance, pp. 17–25. Copyright © 2004 by the American Gastroenterological Association. Published by Elsevier Inc. Published version available at: http://dx.doi.org/10.1053/j.gastro.2004.03.068

Paper III: Familial Cancer 2, Stormorken, Astrid T.; Müller, Wolfram; Lindblom, Annika; Heimdal, Ketil; Aase, Steinar; Bowitz Lothe, Inger Marie; Norèn, Tove; Wijnen, Juul T.; Möslein, Gabriela and Pål Møller, The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours, pp. 9–13. Copyright 2003 Kluwer Academic Publishers/ Springer Verlag. Full-text not available due to publisher restrictions. Published version available at: http://dx.doi.org/10.1023/A:1023362205205

Paper IV: Journal of Pathology 192(3), Leeuw, Wiljo J. F. de; Dierssen, Jan Willem; Vasen, Hans F. A.; Wijnen, Juul Th.; Kenter, Gemma G.;Meijers-Heijboer, Hanne; Brocker-Vriends, Annette; Stormorken, Astrid; Moller, Pal; Menko, Fred; Cornelisse, Cees J. and Hans Morreau, Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients, pp. 328-335. Copyright 2000 John Wiley & Sons, Ltd. Full-text not available due to publisher restrictions. Published version available at: http://dx.doi.org/10.1002/1096-9896(2000)9999:9999<::AID-PATH701>3.0.CO;2-2

Paper V: Familial Cancer 1, Stormorken, Astrid T.; Müller, Wolfram; Lemkemeyer, Britta; Apold, Jaran; Wijnen, Juul T.; Fodde, Riccardo; Möslein Gabriela and Pål Møller, Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry, pp. 169–173. Copyright 2002 Kluwer Academic Publishers/ Springer Verlag. Full-text not available due to publisher restrictions. Published version available at: http://dx.doi.org/10.1023/A:1021151227983

Paper VI: Journal of Clinical Oncology 23(21), Stormorken, Astrid T.; Bowitz-Lothe, Inger Marie; Norèn, Tove; Kure, Elin; Aase, Steinar; Wijnen, Juul; Apold, Jaran; Heimdal, Ketil and Pål Møller, Immunohistochemistry identifies carriers of mismatch repair gene defects causing Hereditary nonpolyposis colorectal cancer, pp. 4705-4712. Copyright © 2005 by American Society of Clinical Oncology. Published version available at: http://dx.doi.org/10.1200/JCO.2005.05.180

Paper VII: Hereditary Cancer in Clinical Practice 4(2), Stormorken, Astrid; Heintz, Karen-Marie; Andresen, Per Arne; Hovig, Eivind; Møller, Pål, MUTYH mutations do not cause HNPCC or late onset familial colorectal cancer, pp. 90-93. Copyright 2006 Termedia Publishing

Paper VIII: Scandinavian Journal of Gastroenterology 41, Stormorken, Astrid T.; Hoff, Jarle Norstein, Inger Marie Bowitz-Lothe, Eldbjørg Hanslien, Eli Grindedal & Pål Møller, Estimated prevalences of hereditary cancers and need for surveillance in a Norwegian county, Telemark, pp. 71-79. Copyright 2006 Taylor & Francis. Published version available at: http://dx.doi.org/10.1080/0036552051002389

Paper IX: Scandinavian Journal of Gastroenterology 42(5), Stormorken, Astrid T.; Clark, Neal; Grindedal, Eli; Mæhle Lovise & Pål Møller, Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer, pp. 611 – 617. Copyright 2007 Taylor & Francis. Published version available at: http://dx.doi.org/10.1080/00365520601010230

Utgiver

The University of Bergen