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    Results: 1 to 20 of 173

    1.

    Frequency of CHEK2 mutations in a population based, case-control study of breast cancer in young women.

    Friedrichsen DM, Malone KE, Doody DR, Daling JR, Ostrander EA.

    Breast Cancer Res. 2004;6(6):R629-35. Epub 2004 Sep 22.

    PMID:
    15535844
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer.

    Vahteristo P, Bartkova J, Eerola H, Syrjäkoski K, Ojala S, Kilpivaara O, Tamminen A, Kononen J, Aittomäki K, Heikkilä P, Holli K, Blomqvist C, Bartek J, Kallioniemi OP, Nevanlinna H.

    Am J Hum Genet. 2002 Aug;71(2):432-8. Epub 2002 Jul 28.

    PMID:
    12094328
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    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.

    Nat Genet. 2002 May;31(1):55-9. Epub 2002 Apr 22.

    PMID:
    11967536
    [PubMed - indexed for MEDLINE]
    4.

    The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.

    Oldenburg RA, Kroeze-Jansema K, Kraan J, Morreau H, Klijn JG, Hoogerbrugge N, Ligtenberg MJ, van Asperen CJ, Vasen HF, Meijers C, Meijers-Heijboer H, de Bock TH, Cornelisse CJ, Devilee P.

    Cancer Res. 2003 Dec 1;63(23):8153-7.

    PMID:
    14678969
    [PubMed - indexed for MEDLINE]
    Free Article
    5.

    Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility.

    Schutte M, Seal S, Barfoot R, Meijers-Heijboer H, Wasielewski M, Evans DG, Eccles D, Meijers C, Lohman F, Klijn J, van den Ouweland A, Futreal PA, Nathanson KL, Weber BL, Easton DF, Stratton MR, Rahman N; Breast Cancer Linkage Consortium.

    Am J Hum Genet. 2003 Apr;72(4):1023-8. Epub 2003 Feb 27.

    PMID:
    12610780
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.

    Bell DW, Kim SH, Godwin AK, Schiripo TA, Harris PL, Haserlat SM, Wahrer DC, Haiman CA, Daly MB, Niendorf KB, Smith MR, Sgroi DC, Garber JE, Olopade OI, Le Marchand L, Henderson BE, Altshuler D, Haber DA, Freedman ML.

    Int J Cancer. 2007 Dec 15;121(12):2661-7.

    PMID:
    17721994
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    7.

    The CHEK2 1100delC mutation is not present in Korean patients with breast cancer cases tested for BRCA1 and BRCA2 mutation.

    Choi DH, Cho DY, Lee MH, Park HS, Ahn SH, Son BH, Haffty BG.

    Breast Cancer Res Treat. 2008 Dec;112(3):569-73. Epub 2008 Jan 3.

    PMID:
    18175216
    [PubMed - indexed for MEDLINE]
    8.

    Absence of CHEK2*1100delC mutation in families with hereditary breast cancer in North America.

    Iniesta MD, Gorin MA, Chien LC, Thomas SM, Milliron KJ, Douglas JA, Merajver SD.

    Cancer Genet Cytogenet. 2010 Oct 15;202(2):136-40.

    PMID:
    20875877
    [PubMed - indexed for MEDLINE]
    9.

    BRCA1/BRCA2 rearrangements and CHEK2 common mutations are infrequent in Italian male breast cancer cases.

    Falchetti M, Lupi R, Rizzolo P, Ceccarelli K, Zanna I, Calò V, Tommasi S, Masala G, Paradiso A, Gulino A, Giannini G, Russo A, Palli D, Ottini L.

    Breast Cancer Res Treat. 2008 Jul;110(1):161-7. Epub 2007 Jul 28.

    PMID:
    17661168
    [PubMed - indexed for MEDLINE]
    10.

    CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls.

    Weischer M, Bojesen SE, Ellervik C, Tybjaerg-Hansen A, Nordestgaard BG.

    J Clin Oncol. 2008 Feb 1;26(4):542-8. Epub 2008 Jan 2. Review.

    PMID:
    18172190
    [PubMed - indexed for MEDLINE]
    11.

    CHEK2 1100delC is not a risk factor for male breast cancer population.

    Syrjäkoski K, Kuukasjärvi T, Auvinen A, Kallioniemi OP.

    Int J Cancer. 2004 Jan 20;108(3):475-6.

    PMID:
    14648717
    [PubMed - indexed for MEDLINE]
    12.

    Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

    Walsh T, Casadei S, Coats KH, Swisher E, Stray SM, Higgins J, Roach KC, Mandell J, Lee MK, Ciernikova S, Foretova L, Soucek P, King MC.

    JAMA. 2006 Mar 22;295(12):1379-88.

    PMID:
    16551709
    [PubMed - indexed for MEDLINE]
    13.

    Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2*1100delC variant.

    de Bock GH, Schutte M, Krol-Warmerdam EM, Seynaeve C, Blom J, Brekelmans CT, Meijers-Heijboer H, van Asperen CJ, Cornelisse CJ, Devilee P, Tollenaar RA, Klijn JG.

    J Med Genet. 2004 Oct;41(10):731-5.

    PMID:
    15466005
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    German populations with infrequent CHEK2*1100delC and minor associations with early-onset and familial breast cancer.

    Rashid MU, Jakubowska A, Justenhoven C, Harth V, Pesch B, Baisch C, Pierl CB, Brüning T, Ko Y, Benner A, Wichmann HE, Brauch H, Hamann U; GENICA Network.

    Eur J Cancer. 2005 Dec;41(18):2896-903. Epub 2005 Oct 18.

    PMID:
    16239104
    [PubMed - indexed for MEDLINE]
    15.

    Germline CHEK2 mutations in Jewish Ashkenazi women at high risk for breast cancer.

    Laitman Y, Kaufman B, Lahad EL, Papa MZ, Friedman E.

    Isr Med Assoc J. 2007 Nov;9(11):791-6.

    PMID:
    18085035
    [PubMed - indexed for MEDLINE]
    Free Article
    16.

    CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.

    CHEK2 Breast Cancer Case-Control Consortium.

    Am J Hum Genet. 2004 Jun;74(6):1175-82. Epub 2004 Apr 30.

    PMID:
    15122511
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    Frequency of BRCA1/BRCA2 mutations in a population-based sample of young breast carcinoma cases.

    Malone KE, Daling JR, Neal C, Suter NM, O'Brien C, Cushing-Haugen K, Jonasdottir TJ, Thompson JD, Ostrander EA.

    Cancer. 2000 Mar 15;88(6):1393-402.

    PMID:
    10717622
    [PubMed - indexed for MEDLINE]
    18.

    Family history, genetic testing, and clinical risk prediction: pooled analysis of CHEK2 1100delC in 1,828 bilateral breast cancers and 7,030 controls.

    Fletcher O, Johnson N, Dos Santos Silva I, Kilpivaara O, Aittomäki K, Blomqvist C, Nevanlinna H, Wasielewski M, Meijers-Heijerboer H, Broeks A, Schmidt MK, Van't Veer LJ, Bremer M, Dörk T, Chekmariova EV, Sokolenko AP, Imyanitov EN, Hamann U, Rashid MU, Brauch H, Justenhoven C, Ashworth A, Peto J.

    Cancer Epidemiol Biomarkers Prev. 2009 Jan;18(1):230-4.

    PMID:
    19124502
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    19.

    The CHEK2*1100delC allelic variant and risk of breast cancer: screening results from the Breast Cancer Family Registry.

    Bernstein JL, Teraoka SN, John EM, Andrulis IL, Knight JA, Lapinski R, Olson ER, Wolitzer AL, Seminara D, Whittemore AS, Concannon P.

    Cancer Epidemiol Biomarkers Prev. 2006 Feb;15(2):348-52.

    PMID:
    16492927
    [PubMed - indexed for MEDLINE]
    Free Article
    20.

    Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals.

    Jekimovs CR, Chen X, Arnold J, Gatei M, Richard DJ, Spurdle AB, Khanna KK, Chenevix-Trench G; kConFab Investigators.

    Br J Cancer. 2005 Feb 28;92(4):784-90.

    PMID:
    15700044
    [PubMed - indexed for MEDLINE]
    Free PMC Article

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