BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 16206141)

  • 1. Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping.
    Ellis NA; Kirchhoff T; Mitra N; Ye TZ; Chuai S; Huang H; Nafa K; Norton L; Neuhausen S; Gordon D; Struewing JP; Narod S; Offit K
    Genet Epidemiol; 2006 Jan; 30(1):48-61. PubMed ID: 16206141
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Localization of cancer susceptibility genes by genome-wide single-nucleotide polymorphism linkage-disequilibrium mapping.
    Mitra N; Ye TZ; Smith A; Chuai S; Kirchhoff T; Peterlongo P; Nafa K; Phillips MS; Offit K; Ellis NA
    Cancer Res; 2004 Nov; 64(21):8116-25. PubMed ID: 15520224
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Haplotype and linkage disequilibrium architecture for human cancer-associated genes.
    Bonnen PE; Wang PJ; Kimmel M; Chakraborty R; Nelson DL
    Genome Res; 2002 Dec; 12(12):1846-53. PubMed ID: 12466288
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels.
    Goode EL; Jarvik GP
    Genet Epidemiol; 2005; 29 Suppl 1():S72-6. PubMed ID: 16342185
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel germline mutations in breast cancer susceptibility genes BRCA1, BRCA2 and p53 gene in breast cancer patients from India.
    Hedau S; Jain N; Husain SA; Mandal AK; Ray G; Shahid M; Kant R; Gupta V; Shukla NK; Deo SS; Das BC
    Breast Cancer Res Treat; 2004 Nov; 88(2):177-86. PubMed ID: 15564800
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
    Gaudet MM; Kirchhoff T; Green T; Vijai J; Korn JM; Guiducci C; Segrè AV; McGee K; McGuffog L; Kartsonaki C; Morrison J; Healey S; Sinilnikova OM; Stoppa-Lyonnet D; Mazoyer S; Gauthier-Villars M; Sobol H; Longy M; Frenay M; GEMO Study Collaborators ; Hogervorst FB; Rookus MA; Collée JM; Hoogerbrugge N; van Roozendaal KE; ; Piedmonte M; Rubinstein W; Nerenstone S; Van Le L; Blank SV; Caldés T; de la Hoya M; Nevanlinna H; Aittomäki K; Lazaro C; Blanco I; Arason A; Johannsson OT; Barkardottir RB; Devilee P; Olopade OI; Neuhausen SL; Wang X; Fredericksen ZS; Peterlongo P; Manoukian S; Barile M; Viel A; Radice P; Phelan CM; Narod S; Rennert G; Lejbkowicz F; Flugelman A; Andrulis IL; Glendon G; Ozcelik H; ; Toland AE; Montagna M; D'Andrea E; Friedman E; Laitman Y; Borg A; Beattie M; Ramus SJ; Domchek SM; Nathanson KL; Rebbeck T; Spurdle AB; Chen X; Holland H; ; John EM; Hopper JL; Buys SS; Daly MB; Southey MC; Terry MB; Tung N; Overeem Hansen TV; Nielsen FC; Greene MH; Mai PL; Osorio A; Durán M; Andres R; Benítez J; Weitzel JN; Garber J; Hamann U; ; Peock S; Cook M; Oliver C; Frost D; Platte R; Evans DG; Lalloo F; Eeles R; Izatt L; Walker L; Eason J; Barwell J; Godwin AK; Schmutzler RK; Wappenschmidt B; Engert S; Arnold N; Gadzicki D; Dean M; Gold B; Klein RJ; Couch FJ; Chenevix-Trench G; Easton DF; Daly MJ; Antoniou AC; Altshuler DM; Offit K
    PLoS Genet; 2010 Oct; 6(10):e1001183. PubMed ID: 21060860
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found.
    Hartikainen JM; Tuhkanen H; Kataja V; Dunning AM; Antoniou A; Smith P; Arffman A; Pirskanen M; Easton DF; Eskelinen M; Uusitupa M; Kosma VM; Mannermaa A
    Cancer Epidemiol Biomarkers Prev; 2005 Jan; 14(1):75-80. PubMed ID: 15668479
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies.
    Gonzalez-Neira A; Rosa-Rosa JM; Osorio A; Gonzalez E; Southey M; Sinilnikova O; Lynch H; Oldenburg RA; van Asperen CJ; Hoogerbrugge N; Pita G; Devilee P; Goldgar D; Benitez J
    BMC Genomics; 2007 Aug; 8():299. PubMed ID: 17760956
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of linkage disequilibrium and its effect on non-parametric multipoint linkage analysis using two high density single-nucleotide polymorphism mapping panels.
    Murray SS
    BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S85. PubMed ID: 16451700
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Linkage disequilibrium maps and disease-association mapping.
    Maniatis N
    Methods Mol Biol; 2007; 376():109-21. PubMed ID: 17984541
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ovarian cancer risk in Ashkenazi Jewish carriers of BRCA1 and BRCA2 mutations.
    Satagopan JM; Boyd J; Kauff ND; Robson M; Scheuer L; Narod S; Offit K
    Clin Cancer Res; 2002 Dec; 8(12):3776-81. PubMed ID: 12473589
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi origin.
    Wolf I; Laitman Y; Rubinek T; Abramovitz L; Novikov I; Beeri R; Kuro-O M; Koeffler HP; Catane R; Freedman LS; Levy-Lahad E; Karlan BY; Friedman E; Kaufman B
    Oncogene; 2010 Jan; 29(1):26-33. PubMed ID: 19802015
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fine mapping by linkage and association in nuclear family and case-control designs.
    Bull SB; John S; Briollais L
    Genet Epidemiol; 2005; 29 Suppl 1():S48-58. PubMed ID: 16342184
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of the progesterone receptor gene with breast cancer risk: a single-nucleotide polymorphism tagging approach.
    Pooley KA; Healey CS; Smith PL; Pharoah PD; Thompson D; Tee L; West J; Jordan C; Easton DF; Ponder BA; Dunning AM
    Cancer Epidemiol Biomarkers Prev; 2006 Apr; 15(4):675-82. PubMed ID: 16614108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes.
    Berry DA; Iversen ES; Gudbjartsson DF; Hiller EH; Garber JE; Peshkin BN; Lerman C; Watson P; Lynch HT; Hilsenbeck SG; Rubinstein WS; Hughes KS; Parmigiani G
    J Clin Oncol; 2002 Jun; 20(11):2701-12. PubMed ID: 12039933
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies.
    Pereira LH; Pineda MA; Rowe WH; Fonseca LR; Greene MH; Offit K; Ellis NA; Zhang J; Collins A; Struewing JP
    BMC Genet; 2007 Oct; 8():68. PubMed ID: 17916242
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%.
    Oddoux C; Struewing JP; Clayton CM; Neuhausen S; Brody LC; Kaback M; Haas B; Norton L; Borgen P; Jhanwar S; Goldgar D; Ostrer H; Offit K
    Nat Genet; 1996 Oct; 14(2):188-90. PubMed ID: 8841192
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association mapping: methodologies, strategies, and issues.
    Havill LM; Dyer TD
    Genet Epidemiol; 2005; 29 Suppl 1():S77-85. PubMed ID: 16342177
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 22(2):121-8. PubMed ID: 12872252
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Short communication: Characterization of the genome-wide linkage disequilibrium in 2 divergent selection lines of dairy cows.
    Banos G; Coffey MP
    J Dairy Sci; 2010 Jun; 93(6):2775-8. PubMed ID: 20494187
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.