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Polymorphisms in DNA repair genes, ionizing radiation exposure and risk of breast cancer in U.S. Radiologic technologists.
Bhatti P, Struewing JP, Alexander BH, Hauptmann M, Bowen L, Mateus-Pereira LH, Pineda MA, Simon SL, Weinstock RM, Rosenstein M, Stovall M, Preston DL, Linet MS, Doody MM, Sigurdson AJ. Bhatti P, et al. Among authors: pineda ma. Int J Cancer. 2008 Jan 1;122(1):177-82. doi: 10.1002/ijc.23066. Int J Cancer. 2008. PMID: 17764108 Free article.
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. Rutter JL, et al. Among authors: pineda ma. Hum Mutat. 2003 Aug;22(2):121-8. doi: 10.1002/humu.10238. Hum Mutat. 2003. PMID: 12872252
CHEK2:1100delC and female breast cancer in the United States.
Mateus Pereira LH, Sigurdson AJ, Doody MM, Pineda MA, Alexander BH, Greene MH, Struewing JP. Mateus Pereira LH, et al. Among authors: pineda ma. Int J Cancer. 2004 Nov 10;112(3):541-3. doi: 10.1002/ijc.20439. Int J Cancer. 2004. PMID: 15382084 Free article. No abstract available.
The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer.
Stredrick DL, Garcia-Closas M, Pineda MA, Bhatti P, Alexander BH, Doody MM, Lissowska J, Peplonska B, Brinton LA, Chanock SJ, Struewing JP, Sigurdson AJ. Stredrick DL, et al. Among authors: pineda ma. Hum Mutat. 2006 Jun;27(6):538-44. doi: 10.1002/humu.20323. Hum Mutat. 2006. PMID: 16652348 Free PMC article.
Skewed X chromosome inactivation and early-onset breast cancer.
Struewing JP, Pineda MA, Sherman ME, Lissowska J, Brinton LA, Peplonska B, Bardin-Mikolajczak A, Garcia-Closas M. Struewing JP, et al. Among authors: pineda ma. J Med Genet. 2006 Jan;43(1):48-53. doi: 10.1136/jmg.2005.033134. Epub 2005 May 27. J Med Genet. 2006. PMID: 15923273 Free PMC article.
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. Pereira LH, et al. Among authors: pineda ma. BMC Genet. 2007 Oct 4;8:68. doi: 10.1186/1471-2156-8-68. BMC Genet. 2007. PMID: 17916242 Free PMC article.
89 results