17 results for author:"Szabo C.I." in Literature citations
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| Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction. Antoniou A.C., Beesley J., McGuffog L., Sinilnikova O.M., Healey S., Neuhausen S.L., Ding Y.C., Rebbeck T.R., Weitzel J.N., Lynch H.T. et al. Cancer Res. 70:9742-9754(2010) · Mapped (18) |
| Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers. Walker L.C., Fredericksen Z.S., Wang X., Tarrell R., Pankratz V.S., Lindor N.M., Beesley J., Healey S., Chen X., Stoppa-Lyonnet D. et al. Breast Cancer Res. 12:R102-R102(2010) · Mapped (6) |
| Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab) Cancer Epidemiol. Biomarkers Prev. 19:2859-2868(2010) · Mapped (21) |
| A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. Antoniou A.C., Wang X., Fredericksen Z.S., McGuffog L., Tarrell R., Sinilnikova O.M., Healey S., Morrison J., Kartsonaki C., Lesnick T. et al. Nat. Genet. 42:885-892(2010) · Mapped (4) |
| Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers. Wang X., Pankratz V.S., Fredericksen Z., Tarrell R., Karaus M., McGuffog L., Pharaoh P.D., Ponder B.A., Dunning A.M., Peock S. et al. Hum. Mol. Genet. 19:2886-2897(2010) · Mapped (29) |
| Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). Osorio A., Milne R.L., Pita G., Peterlongo P., Heikkinen T., Simard J., Chenevix-Trench G., Spurdle A.B., Beesley J., Chen X. et al. Br. J. Cancer 101:2048-2054(2009) · Mapped (22) |
| Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer Hum. Mol. Genet. 18:4442-4456(2009) · Mapped (25) |
| Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. Kathleen Cuningham Consortium for Research into Familial Breast Cancer Am. J. Hum. Genet. 82:937-948(2008) · Mapped (20) |
| RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. German Consortium for Hereditary Breast and Ovarian Cancer (GCHBOC) Am. J. Hum. Genet. 81:1186-1200(2007) · Mapped (25) |
| Contribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India. Saxena S., Chakraborty A., Kaushal M., Kotwal S., Bhatanager D., Mohil R.S., Chintamani C., Aggarwal A.K., Sharma V.K., Sharma P.C. et al. BMC Med. Genet. 7:75-75(2006) · Mapped (18) |
| BRCA1 and BRCA2 in Indian breast cancer patients. Saxena S., Szabo C.I., Chopin S., Barjhoux L., Sinilnikova O., Lenoir G., Goldgar D.E., Bhatanager D. |
| Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1. Smith T.M., Lee M.K., Szabo C.I., Jerome N., McEuen M., Taylor M., Hood L., King M.-C. Genome Res. 6:1029-1049(1996) · UniProtKB (4) |
| Human, canine and murine BRCA1 genes: sequence comparison among species. Szabo C.I., Wagner L.A., Francisco L.V., Roach J.C., Argonza R., King M.-C., Ostrander E.A. Hum. Mol. Genet. 5:1289-1298(1996) · UniProtKB (2) · Mapped (6) |
| BRCA1 is secreted and exhibits properties of a granin. Jensen R.A., Thompson M.E., Jetton T.L., Szabo C.I., van der Meer R., Helou B., Tronick S.R., Page D.L., King M.C., Holt J.T. Nat. Genet. 12:303-308(1996) · Mapped (5) |
| Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families. Friedman L.S., Szabo C.I., Ostermeyer E.A., Dowd P., Butler L., Park T., Lee M.K., Goode E.L., Rowell S.E., King M.C. Am. J. Hum. Genet. 57:1284-1297(1995) · UniProtKB (1) |
| Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Friedman L.S., Ostermeyer E.A., Szabo C.I., Dowd P., Lynch E.D., Rowell S.E., King M.-C. Nat. Genet. 8:399-404(1994) · UniProtKB (1) |
| 22 genes from chromosome 17q21: cloning, sequencing, and characterization of mutations in breast cancer families and tumors. Friedman L.S., Ostermeyer E.A., Lynch E.D., Szabo C.I., Meza J.E., Anderson L.A., Dowd P., Lee M.K., Rowell S.E., Ellison J. et al. Genomics 25:256-263(1995) · UniProtKB (2) |