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133 related items for PubMed ID: 18663745

  • 1. Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.
    Oldenburg RA, Kroeze-Jansema KH, Houwing-Duistermaat JJ, Bayley JP, Dambrot C, van Asperen CJ, van den Ouweland AM, Bakker B, van Beers EH, Nederlof PM, Vasen H, Hoogerbrugge N, Cornelisse CJ, Meijers-Heijboer H, Devilee P.
    Genes Chromosomes Cancer; 2008 Nov; 47(11):947-56. PubMed ID: 18663745
    [Abstract] [Full Text] [Related]

  • 2. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families.
    Arason A, Gunnarsson H, Johannesdottir G, Jonasson K, Bendahl PO, Gillanders EM, Agnarsson BA, Jönsson G, Pylkäs K, Mustonen A, Heikkinen T, Aittomäki K, Blomqvist C, Melin B, Johannsson OT, Møller P, Winqvist R, Nevanlinna H, Borg A, Barkardottir RB.
    Breast Cancer Res; 2010 Nov; 12(4):R50. PubMed ID: 20637093
    [Abstract] [Full Text] [Related]

  • 3. CGH analysis of familial non-BRCA1/BRCA2 breast tumors and mutation screening of a candidate locus on chromosome 17q11.2-12.
    Maguire P, Holmberg K, Kost-Alimova M, Imreh S, Skoog L, Lindblom A.
    Int J Mol Med; 2005 Jul; 16(1):135-41. PubMed ID: 15942690
    [Abstract] [Full Text] [Related]

  • 4. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.
    Kainu T, Juo SH, Desper R, Schaffer AA, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi OP, Tirkkonen M, Syrjäkoski K, Kuukasjärvi T, Koivisto P, Karhu R, Holli K, Arason A, Johannesdottir G, Bergthorsson JT, Johannsdottir H, Egilsson V, Barkardottir RB, Johannsson O, Haraldsson K, Sandberg T, Holmberg E, Grönberg H, Olsson H, Borg A, Vehmanen P, Eerola H, Heikkila P, Pyrhönen S, Nevanlinna H.
    Proc Natl Acad Sci U S A; 2000 Aug 15; 97(17):9603-8. PubMed ID: 10944226
    [Abstract] [Full Text] [Related]

  • 5. Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer.
    Marikkannu R, Aravidis C, Rantala J, Picelli S, Adamovic T, Keihas M, Liu T, Kontham V, Nilsson D, Lindblom A.
    Anticancer Res; 2015 Jun 15; 35(6):3155-65. PubMed ID: 26026075
    [Abstract] [Full Text] [Related]

  • 6. Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: suggestive linkage to 10q23.32-q25.3.
    Bergman A, Karlsson P, Berggren J, Martinsson T, Björck K, Nilsson S, Wahlström J, Wallgren A, Nordling M.
    Genes Chromosomes Cancer; 2007 Mar 15; 46(3):302-9. PubMed ID: 17171685
    [Abstract] [Full Text] [Related]

  • 7. Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.
    Rosa-Rosa JM, Pita G, Urioste M, Llort G, Brunet J, Lázaro C, Blanco I, Ramón y Cajal T, Díez O, de la Hoya M, Caldés T, Tejada MI, González-Neira A, Benítez J.
    Am J Hum Genet; 2009 Feb 15; 84(2):115-22. PubMed ID: 19147119
    [Abstract] [Full Text] [Related]

  • 8. Characterization of familial non-BRCA1/2 breast tumors by loss of heterozygosity and immunophenotyping.
    Oldenburg RA, Kroeze-Jansema K, Meijers-Heijboer H, van Asperen CJ, Hoogerbrugge N, van Leeuwen I, Vasen HF, Cleton-Jansen AM, Kraan J, Houwing-Duistermaat JJ, Morreau H, Cornelisse CJ, Devilee P.
    Clin Cancer Res; 2006 Mar 15; 12(6):1693-700. PubMed ID: 16551851
    [Abstract] [Full Text] [Related]

  • 9. A genome wide linkage search for breast cancer susceptibility genes.
    Smith P, McGuffog L, Easton DF, Mann GJ, Pupo GM, Newman B, Chenevix-Trench G, kConFab Investigators, Szabo C, Southey M, Renard H, Odefrey F, Lynch H, Stoppa-Lyonnet D, Couch F, Hopper JL, Giles GG, McCredie MR, Buys S, Andrulis I, Senie R, BCFS, BRCAX Collaborators Group, Goldgar DE, Oldenburg R, Kroeze-Jansema K, Kraan J, Meijers-Heijboer H, Klijn JG, van Asperen C, van Leeuwen I, Vasen HF, Cornelisse CJ, Devilee P, Baskcomb L, Seal S, Barfoot R, Mangion J, Hall A, Edkins S, Rapley E, Wooster R, Chang-Claude J, Eccles D, Evans DG, Futreal P, Nathanson KL, Weber BL, Breast Cancer Susceptibility Collaboration (UK), Rahman N, Stratton MR.
    Genes Chromosomes Cancer; 2006 Jul 15; 45(7):646-55. PubMed ID: 16575876
    [Abstract] [Full Text] [Related]

  • 10. Prediction of BRCA2-association in hereditary breast carcinomas using array-CGH.
    Joosse SA, Brandwijk KI, Devilee P, Wesseling J, Hogervorst FB, Verhoef S, Nederlof PM.
    Breast Cancer Res Treat; 2012 Apr 15; 132(2):379-89. PubMed ID: 20614180
    [Abstract] [Full Text] [Related]

  • 11. Genetic heterogeneity in hereditary breast cancer: role of BRCA1 and BRCA2.
    Rebbeck TR, Couch FJ, Kant J, Calzone K, DeShano M, Peng Y, Chen K, Garber JE, Weber BL.
    Am J Hum Genet; 1996 Sep 15; 59(3):547-53. PubMed ID: 8751855
    [Abstract] [Full Text] [Related]

  • 12. Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?
    Serova OM, Mazoyer S, Puget N, Dubois V, Tonin P, Shugart YY, Goldgar D, Narod SA, Lynch HT, Lenoir GM.
    Am J Hum Genet; 1997 Mar 15; 60(3):486-95. PubMed ID: 9042907
    [Abstract] [Full Text] [Related]

  • 13. Genome-wide scanning for linkage in Finnish breast cancer families.
    Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, Leisti J, Blanco G, Puistola U, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi OP.
    Eur J Hum Genet; 2004 Feb 15; 12(2):98-104. PubMed ID: 14560309
    [Abstract] [Full Text] [Related]

  • 14. A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer.
    Djureinovic T, Skoglund J, Vandrovcova J, Zhou XL, Kalushkova A, Iselius L, Lindblom A.
    Gut; 2006 Mar 15; 55(3):362-6. PubMed ID: 16150854
    [Abstract] [Full Text] [Related]

  • 15. RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families.
    Larsen MJ, Thomassen M, Tan Q, Lænkholm AV, Bak M, Sørensen KP, Andersen MK, Kruse TA, Gerdes AM.
    BMC Med Genomics; 2014 Jan 31; 7():9. PubMed ID: 24479546
    [Abstract] [Full Text] [Related]

  • 16. BRCA1 and BRCA2 unclassified variants and missense polymorphisms in Algerian breast/ovarian cancer families.
    Cherbal F, Salhi N, Bakour R, Adane S, Boualga K, Maillet P.
    Dis Markers; 2012 Jan 31; 32(6):343-53. PubMed ID: 22684231
    [Abstract] [Full Text] [Related]

  • 17. Statewide Retrospective Review of Familial Pancreatic Cancer in Delaware, and Frequency of Genetic Mutations in Pancreatic Cancer Kindreds.
    Catts ZA, Baig MK, Milewski B, Keywan C, Guarino M, Petrelli N.
    Ann Surg Oncol; 2016 May 31; 23(5):1729-35. PubMed ID: 26727920
    [Abstract] [Full Text] [Related]

  • 18. Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer.
    Machackova E, Foretova L, Lukesova M, Vasickova P, Navratilova M, Coene I, Pavlu H, Kosinova V, Kuklova J, Claes K.
    BMC Cancer; 2008 May 20; 8():140. PubMed ID: 18489799
    [Abstract] [Full Text] [Related]

  • 19. Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer.
    Cavallone L, Arcand SL, Maugard CM, Nolet S, Gaboury LA, Mes-Masson AM, Ghadirian P, Provencher D, Tonin PN.
    Fam Cancer; 2010 Dec 20; 9(4):507-17. PubMed ID: 20694749
    [Abstract] [Full Text] [Related]

  • 20. Mapping of a novel ocular and cutaneous malignant melanoma susceptibility locus to chromosome 9q21.32.
    Jönsson G, Bendahl PO, Sandberg T, Kurbasic A, Staaf J, Sunde L, Crüger DG, Ingvar C, Olsson H, Borg A.
    J Natl Cancer Inst; 2005 Sep 21; 97(18):1377-82. PubMed ID: 16174859
    [Abstract] [Full Text] [Related]

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