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A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland.
Cybulski C, Wokołorczyk D, Huzarski T, Byrski T, Gronwald J, Górski B, Debniak T, Masojć B, Jakubowska A, van de Wetering T, Narod SA, Lubiński J. Cybulski C, et al. Among authors: narod sa. Breast Cancer Res Treat. 2007 Mar;102(1):119-22. doi: 10.1007/s10549-006-9320-y. Epub 2006 Aug 8. Breast Cancer Res Treat. 2007. PMID: 16897426
BRCA2 hereditary breast cancer pathophenotype.
Marcus JN, Watson P, Page DL, Narod SA, Tonin P, Lenoir GM, Serova O, Lynch HT. Marcus JN, et al. Among authors: narod sa. Breast Cancer Res Treat. 1997 Jul;44(3):275-7. doi: 10.1023/a:1005830230664. Breast Cancer Res Treat. 1997. PMID: 9266108 No abstract available.
Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer.
Górski B, Byrski T, Huzarski T, Jakubowska A, Menkiszak J, Gronwald J, Pluzańska A, Bebenek M, Fischer-Maliszewska L, Grzybowska E, Narod SA, Lubiński J. Górski B, et al. Among authors: narod sa. Am J Hum Genet. 2000 Jun;66(6):1963-8. doi: 10.1086/302922. Epub 2000 Apr 28. Am J Hum Genet. 2000. PMID: 10788334 Free PMC article.
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.
Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N, Stratton MR; CHEK2-Breast Cancer Consortium. Meijers-Heijboer H, et al. Nat Genet. 2002 May;31(1):55-9. doi: 10.1038/ng879. Epub 2002 Apr 22. Nat Genet. 2002. PMID: 11967536
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.
Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, Loman N, Olsson H, Johannsson O, Borg A, Pasini B, Radice P, Manoukian S, Eccles DM, Tang N, Olah E, Anton-Culver H, Warner E, Lubinski J, Gronwald J, Gorski B, Tulinius H, Thorlacius S, Eerola H, Nevanlinna H, Syrjäkoski K, Kallioniemi OP, Thompson D, Evans C, Peto J, Lalloo F, Evans DG, Easton DF. Antoniou A, et al. Am J Hum Genet. 2003 May;72(5):1117-30. doi: 10.1086/375033. Epub 2003 Apr 3. Am J Hum Genet. 2003. PMID: 12677558 Free PMC article.
Heterozygosity for the BLM(Ash) mutation and cancer risk.
Cleary SP, Zhang W, Di Nicola N, Aronson M, Aube J, Steinman A, Haddad R, Redston M, Gallinger S, Narod SA, Gryfe R. Cleary SP, et al. Among authors: narod sa. Cancer Res. 2003 Apr 15;63(8):1769-71. Cancer Res. 2003. PMID: 12702560
Hereditary ovarian cancer in Poland.
Menkiszak J, Gronwald J, Górski B, Jakubowska A, Huzarski T, Byrski T, Foszczyńska-Kłoda M, Haus O, Janiszewska H, Perkowska M, Brozek I, Grzybowska E, Zientek H, Góźdź S, Kozak-Klonowska B, Urbański K, Miturski R, Kowalczyk J, Pluzańska A, Niepsuj S, Koc J, Szwiec M, Drosik K, Mackiewicz A, Lamperska K, Strózyk E, Godlewski D, Stawicka M, Waśko B, Bebenek M, Rozmiarek A, Rzepka-Górska I, Narod SA, Lubiński J. Menkiszak J, et al. Among authors: narod sa. Int J Cancer. 2003 Oct 10;106(6):942-5. doi: 10.1002/ijc.11338. Int J Cancer. 2003. PMID: 12918074 Free article.
888 results