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PUBMED FOR HANDHELDS

Journal Abstract Search


212 related items for PubMed ID: 16825437

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  • 11. Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer.
    Weber-Lassalle N, Borde J, Weber-Lassalle K, Horváth J, Niederacher D, Arnold N, Kaulfuß S, Ernst C, Paul VG, Honisch E, Klaschik K, Volk AE, Kubisch C, Rapp S, Lichey N, Altmüller J, Lepkes L, Pohl-Rescigno E, Thiele H, Nürnberg P, Larsen M, Richters L, Rhiem K, Wappenschmidt B, Engel C, Meindl A, Schmutzler RK, Hahnen E, Hauke J.
    Breast Cancer Res; 2019 Apr 29; 21(1):55. PubMed ID: 31036035
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  • 13. Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals.
    Kuusisto KM, Bebel A, Vihinen M, Schleutker J, Sallinen SL.
    Breast Cancer Res; 2011 Feb 28; 13(1):R20. PubMed ID: 21356067
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  • 14. Mutation screening of the BARD1 gene: evidence for involvement of the Cys557Ser allele in hereditary susceptibility to breast cancer.
    Karppinen SM, Heikkinen K, Rapakko K, Winqvist R.
    J Med Genet; 2004 Sep 28; 41(9):e114. PubMed ID: 15342711
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  • 17. BARD1 Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort.
    Rofes P, Del Valle J, Torres-Esquius S, Feliubadaló L, Stradella A, Moreno-Cabrera JM, López-Doriga A, Munté E, De Cid R, Campos O, Cuesta R, Teulé Á, Grau È, Sanz J, Capellá G, Díez O, Brunet J, Balmaña J, Lázaro C.
    Genes (Basel); 2021 Jan 23; 12(2):. PubMed ID: 33498765
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  • 18. Literature Review of BARD1 as a Cancer Predisposing Gene with a Focus on Breast and Ovarian Cancers.
    Alenezi WM, Fierheller CT, Recio N, Tonin PN.
    Genes (Basel); 2020 Jul 27; 11(8):. PubMed ID: 32726901
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  • 20. Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals.
    Rutter JL, Smith AM, Dávila MR, Sigurdson AJ, Giusti RM, Pineda MA, Doody MM, Tucker MA, Greene MH, Zhang J, Struewing JP.
    Hum Mutat; 2003 Aug 27; 22(2):121-8. PubMed ID: 12872252
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