Cite

Anonīms (2007). Latvijas vēža registrs [Cancer Registry of Latvia]. Riga, Latvia (in Latvian).Search in Google Scholar

Anonymous (2002). Globocan 2002. International Agency for Research on Cancer. http://www-dep.iarc.fr/globocan/globocan.htmlSearch in Google Scholar

Aretz, S., Stienen, D., Friedrichs, N., Stemmler, S., Uhlhaas, S., Rahner, N., Friedl, W. (2007). Somatic APC mosaicism: A frequent cause of familial adenomatous polyposis (FAP). Hum. Mutat., 28(10), 985-992.10.1002/humu.2054917486639Search in Google Scholar

Bartch, D.K., Kress, R., Sina-Frey, M., Grutzman, R., Gerdes, B., Pilarsky, C., Heise, J.V., Schulte, K.M., Ghadimi, M.B., Horstmann, O., Schmidt, J., Eisold, S., Hahn, S.A., Schulmann, K., Bock, W., Gress, T.M., Zugel, N., Prenzel, K., Messmann, H., Enlicher, E., Schneider, M., Ziegler, M., Schmiegel, K., Rothmund, M., Rieder, H. (2004). Epidemiology. Prevalence of familial pancreatic cancer in Germany. Int. J. Cancer, 110(6), 902-906.Search in Google Scholar

Bisgaard, M., Ripa, R., Bülow, S. (2004). Mutation analysis of the adenomatous polyposis coli (APC) gene in Danish patients with familial adenomatous polyposis (FAP). Human Mutation: Mutation in Brief, No. 705, http://www3.interscience.wiley.com/homepages/38515/pdf/mutation/705.pdf http://www3.interscience.wiley.com/homepages/38515/pdf/mutation/705.pdf10.1002/humu.923415108286Search in Google Scholar

Boltenberg, A., Furgyik, S., Kullander, S. (1990). Familial cancer agregation in cases of adenocarcinoma corporis uteri. Acta Obstet. Gynecol. Scand., 69, 249-258.10.3109/000163490090286892220348Search in Google Scholar

Bratt, O. (2000). Hereditary prostate cancer. BJU Int. 85(5), 588-98.10.1046/j.1464-410x.2000.00457.x10735934Search in Google Scholar

Bülow, S., Nielsen, T., Bülow, C., Bisgaard, M.L., Karlsen, L., Moesgaard, F. (1996). The incidence rate of familial adenomatous polyposis. Results from the Danish Polyposis Register. Int. J. Colorectal Dis., 11(2), 88-91.Search in Google Scholar

Calin, G.A., Trapasso, F., Shimizu, M., Dumitru, C.D., Godwin, A.K., Ferracin, M., Bernardi, G., Rattan, S., Alder, H., Mabuchi, H., Overgaard, J., Mauro, F.R., Neuberg, D., Bullrich, F., Negrini, M., Croce, C.M. (2005). Familial cancer associated with a polymorphism in ARLTS1. New Engl. J. Med., 352, 1667-1676.10.1056/NEJMoa04228015843669Search in Google Scholar

Chapelle, A., de la (2004). Genetic predisposition to colorectal cancer. Nat. Rev. Cancer., 4(10), 769-780.10.1038/nrc145315510158Search in Google Scholar

Chiaro, M., Presciuttini, S., Bertacca, L., Zerbi, A., Longoni, B.M., Cipollini, G., Caligo, M.A., Boggi, U., Civitelli, V., Falconi, M., Pederzoli, P., Di Carlo, V., Cavallini, G., Mosca, F. (2005). Cancer risk among relatives of probands with pancreatic ductal adenocarcinoma. Offic. J. Int. HepatoPancreatoBiliary Assoc., 7(1), 76.Search in Google Scholar

Csokay, B., Tihomirova, L., Stengrevics, A., Sinicka, O., Olah, E. (1999). Strong founder effects in BRCA1 mutation carrier breast cancer patients from Latvia. Hum. Mutat., 14, 92.Search in Google Scholar

Cybulski, C., Górski, B., Debniak, T., Gliniewicz, B., Mierzejewski, M., Masojc, B., Jakubowska, A., Matyjasik, J., Zlowocka, E., Sikorski, A., Narod, S.A., Lubinski, J. (2004). NBS1 is a prostate cancer susceptibility gene. Cancer Res., 64(4), 1215-1219.10.1158/0008-5472.CAN-03-250214973119Search in Google Scholar

Cybulski, C., Huzarski, T., Górski, B., Masojc, B., Mierzejewski, M., Debniak, T., Gliniewicz, B., Matyjasik, J., Zlowocka, E., Kurzawski, G., Sikorski, A., Posmyk, M., Szwiec, M., Czajka, R., Narod, S.A., Lubinski, J. (2004). A novel founder CHEK2 mutation is associated with increased prostate cancer risk. Cancer Res., 64(8), 2677-2679.10.1158/0008-5472.CAN-04-034115087378Search in Google Scholar

Cybulski, C., Górski, B., Gronwald, J., Huzarski, T., Byrski, T., Debniak, T., Jakubowska, A., Wokolorczyk, D., Gliniewicz, B., Sikorski, A., Stawicka, M., Godlewski, D., Kwias, Z., Antczak, A., Borkowski, T., Szwiec, M., Posmyk, M., Narod, S.A., Lubiński, J. (2008). BRCA1 mutations and prostate cancer in Poland. Eur. J. Cancer Prev., 17, 62-66.10.1097/CEJ.0b013e32809b4d2018090912Search in Google Scholar

Debniak, T., Scott, R.J., Huzarski, T., Byrski, T., Rozmiarek, A., Debniak, B., Gorski, B., Cybulski, C., Medrek, K., Masojc, B., Lener, M., Jaworowska, E., Oszutowska, D., Szymanska, A., Castaneda, J., Wetering, T., Suchy, J., Kurzawski, G., Oszurek, O., Narod, S., Lubinski, J. (2006). CDKN2A common variant and multi-organ cancer risk - a population-based study. Int. J. Cancer, 118(12), 3180-3182.10.1002/ijc.2176016395703Search in Google Scholar

Debniak, T., Cybulski, C., Kurzawski, G., Górski, B., Huzarski, T. (2006). Low-risk genes and multi-organ cancer risk in the Polish population. Hered. Cancer Clin. Pract., 4(1), 52-55.10.1186/1897-4287-4-1-52340192220223005Search in Google Scholar

Ford, D., Easton, D.F., Stratton, M., Narod, S., Goldgar, D. (1998). Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. Amer. J. Hum. Genet., 62(3), 676-689.10.1086/30174913769449497246Search in Google Scholar

Frank, B., Hemminki, K., Meindl, A., Wappenschmidt, B., Klaes, R., Schmutzler, R., Untch, M., Bugert, P., Bartram, C.R., Burwinkel, B. (2006). Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk. Int. J. Cancer, 118, 2505-2508.10.1002/ijc.2168716353159Search in Google Scholar

Fromont, G., Yacoub, M., Valeri, A., Mangin, P., Vallancien, G., Cancel-Tassin, G., Cussenot, O. (2008). Differential expression of genes related to androgen and estrogen metabolism in hereditary versus sporadic prostate cancer. Cancer Epidemiol Biomarkers Prev., 17, 1505-1509.10.1158/1055-9965.EPI-07-277818559568Search in Google Scholar

Górski, B., Byrski, T., Huzarski, T. (2000). Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer. Amer. J. Hum. Genet., 66, 1963-1968.10.1086/302922137805110788334Search in Google Scholar

Gronwald, J., Huzarski, T., Oszurek, O., Janicka, A., Szymańska-Pasternak, J., Górski, B., Menkiszak, J., Rzepka-Górska, I., Lubiński, J. (2008). Hereditary breast and ovarian cancer. Hered. Cancer Clin. Pract., 6(2), 88-98.10.1186/1897-4287-6-2-88273578419804604Search in Google Scholar

Gronwald, J., Elsakob, P., Gorski, B., Lubinski, J. (2005). High incidence of 4153delA BRCA1 gene mutations in Lithuanian breast- and breast-ovarian cancer families. Breast Cancer Res. Treat., 94(2), 111-113.10.1007/s10549-005-5150-616261409Search in Google Scholar

Hahn, S.A., Greenhalf, B., Ellis, I., Sine-frey, M., Rieder, H., Korte, B., Gerdes, B., Kress, R., Ziegler, A., Campra, D., Grutzmann, R., Rehder, H., Rothmund, M., Schmiegel, W., Neoptolemos, J.P., Bartsch, D.K. (2003). BRCA2 germline mutations in familial pancreatic carcinoma. J. Natl. Cancer Ins., 95, 214-221.10.1093/jnci/95.3.21412569143Search in Google Scholar

Hughes, C., Murphy, A., Martin, C., Sheils, O., O'Leary, J. (2005). Molecular pathology of prostate cancer. J. Clin. Pathol., 58, 673-684.10.1136/jcp.2002.003954177071515976331Search in Google Scholar

Jarvinen, H.J. (1992). Epidemiology of familial adenomatous polyposis in Finland: Impact of family screening on the colorectal cancer rate and survival. Gut, 33(3), 357-360.10.1136/gut.33.3.35713738271314763Search in Google Scholar

Jacobi, C.E., Jonker, M.A., Nagelkerke, N., van Houwelingen, J., Bock, G.H. (2003). Prevalence of family histories of breast cancer in the general population and the incidence of related seeking of health care. J. Med. Genet., 40(7), e83.10.1136/jmg.40.7.e83Search in Google Scholar

Jemal, A., Thomas, A., Murray, T., Thun, M. (2002). Cancer statistics. Ca. Cancer J. Clin., 52, 23-47.10.3322/canjclin.52.1.23Search in Google Scholar

John, E.M. (2004). The Breast Cancer Family Registry: An infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer. Breast Cancer Res., 6(4), R375-389.10.1186/bcr801Search in Google Scholar

Kilpivaara, O., Laiho, L., Aaltonen, A., Nevanlinna, H. (2003). CHEK2 1100delC and colorectal cancer. J. Med. Genet., 40(10), 110.10.1136/jmg.40.10.e110Search in Google Scholar

Kurzawski, G., Suchy, J., Kladny, J., Grabowska, E., Jakubowska, A., Debniak, T., Cybulski, C., Kowalska, E., Szych, Z., Domagala, W., Scott, R.J., Lubinski, J. (2004). The NOD2 3020insC mutation and the risk of colorectal cancer. Cancer Res. 64(5), 1604-1606.10.1158/0008-5472.CAN-03-3791Search in Google Scholar

Levy-Lahad, E. (1997). Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: Frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families. Amer. J. Hum. Genet., 60(5), 1059-1067.Search in Google Scholar

Lichtenstein, P., Holm, N.V., Verkasalo, P.K., Iliadou, A., Kaprio, J., Koskenvuo M., Pukkala E., Hemminki, K. (2000). Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland. New Engl. J. Med., 343, 78-85.10.1056/NEJM200007133430201Search in Google Scholar

Lynch, H.T., Lanspa, S., Smyrk, B.B., Watson, P., Lynch, J. (1991). Hereditary non-polyposis colorectal cancer (Lynch syndromes I and II) genetics, pathology, natural history and cancer control, Part I. Cancer Genet. Cytogenetic., 53, 143-160.10.1016/0165-4608(91)90093-ASearch in Google Scholar

Martin, A.M., Blackwood, M.A., Antin-Ozerkis, D., Shih, H.A., Calzone, K., Colligon, T., Seal, S., Collins, N., Stratton, M.R., Weber, B.L., Nathanson, K.L. (2001). Germline mutations in BRCA1 and BRCA2 in breast-ovarian families from a breast cancer risk evaluation clinic. J. Clin. Oncol., 19(8), 2247-2253.10.1200/JCO.2001.19.8.2247Search in Google Scholar

Masojc, B., Mierzejewski, M., Cybulski, C., Wetering, T., Debniak, T., Gorski, B., Jaworowska, E., Tarnowska, C., Lenner, M., Scott, R.J., Lubinski, J. (2006). Cancer Familial Aggregation (CFA) and G446A polymorphism in ARLTS1 gene. Breast Cancer Res. Treat., 99(1), 59-62.10.1007/s10549-006-9180-5Search in Google Scholar

Mecklin, J.-P., Jarvinen, H.I. (1991). Tumor spectrum in cancer-family syndroma. Cancer, 68, 1109-1112.10.1002/1097-0142(19910901)68:5<1109::AID-CNCR2820680535>3.0.CO;2-SSearch in Google Scholar

Ogura, Y., Bonen, D.K., Inohara, N., Nicolae, D.L., Chen, F.F., Ramos, R., Britton, H., Moran, T., Duerr, R., Achkar, R., Brant, S., Bayless, T., Kirschner, B., Hanauer, S., Nunez, G., Cho, J.H. (2001). A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature, 411(6837), 603-606.Search in Google Scholar

Oszurek, O., Gorski, B., Gronwald, J., Prosolow, Z., Uglanica, K., Murinow, A., Bobko, I., Norik, D., Byrski, T., Jakubowska, A., Lubinski, J. (2001). Founder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families. Clin. Genet., 60(6), 470-471.10.1034/j.1399-0004.2001.600611.xSearch in Google Scholar

Ollikainen, M., Abdel-Rahman, W., Moisio, A., Lindroos, A., Kariola, R., Jarvela, I., Poyhonen, M., Butzow, R., Peltomaki, P. (2005). Molecular analysis of familial endometrial carcinoma: A manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome. J. Clin. Oncol., 23(21), 4609-4616.10.1200/JCO.2005.06.055Search in Google Scholar

Pohlreich, P. (2005). High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area. Breast Cancer Res., 7(5), R728-736.10.1186/bcr1282Search in Google Scholar

Rennert, H., Zeigler-Johnson, C., Addya, K., Finley, M., Walker, A., Spangler, E., Leonard, D., Wein, A., Malkowicz, S., Rebbeck, T. (2005). Association of susceptibility alleles in ELAC2/HPC2, RNASEL/HPC1, and MSR1 with prostate cancer severity in European American and African American men. Cancer Epidemiol. Biomarkers Prev., 14(4), 949-957.10.1158/1055-9965.EPI-04-0637Search in Google Scholar

Sandles, L.G. (1998). Familial endometrial adenocarcinoma. Clin. Obstet. Gynecol., 41, 167-171.10.1097/00003081-199803000-00023Search in Google Scholar

Santarosa, M., Liede, A., Aube, J., Finch, A., Kwan, E., Jack, E., Narod, S., Randall, S., Hugel, L., Clark, K. (1999). BRCA1 and BRCA2 genes: Role in hereditary breast and ovarian cancer in Italy. Int. J. Cancer, 83(1), 5-9.10.1002/(SICI)1097-0215(19990924)83:1<5::AID-IJC2>3.0.CO;2-USearch in Google Scholar

Sinicka, O., Stengrevics, A., Eglitis, J., Smite, D., Shomshteine, Z., Tihomirova, L. (2004). Ovarian cancer in Latvia is attributable to recurrent mutations in the BRCA1 gene. Acta Universitatis Latviensis. Biology, 676, 17-25.Search in Google Scholar

Suomi, R., Hakala, T., Pietila, A., Laminen, A., Mecklin, J.-P., Lehtovirta, P. (1995). Hereditary aspects of endometrial adenocarcinoma. J. Cancer, 62, 132-137.10.1002/ijc.2910620204Search in Google Scholar

Stacey, S.N., Sulem, P., Johannsson, O., Helgason, A., Gudmundsson, J., Kostic, J., Kristjansson, K., Sveinsson, T., Myrdal, G., Grimsson, H., Kong, A., Stefansson, K. (2006). The BARD1 Cys557Ser variant and breast cancer risk in Iceland. PLoS Med., 3(7), e217.10.1371/journal.pmed.0030217Search in Google Scholar

Thompson, D., Easton, D.F. (2002). Cancer incidence in BRCA1 mutation carriers. J. Natl. Cancer Inst., 94(18), 1358-1365.10.1093/jnci/94.18.1358Search in Google Scholar

Tikhomirova, L., Sinicka, O., Smite, D., Hodgson, S.V., Stengrevics, A. (2005). High prevalence of two BRCA1 mutations, 4154delA and 5382insC in Latvia. Fam. Cancer, 4, 77-84.10.1007/s10689-004-2758-3Search in Google Scholar

Vasen, H.F. (2001). Erfelijke tumoren. Richtlijnen voor diagnostiek en preventie. Stichting Opsporing Erfelijke Tumoren & Vereniging klinische Genetica Nederland Werkgroep Klinische Oncogenetica. 21.Search in Google Scholar

ISSN:
1407-009X
Language:
English
Publication timeframe:
6 times per year
Journal Subjects:
General Interest, Mathematics, General Mathematics