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Performance of Amplified DNA in an Illumina GoldenGate BeadArray AssayCUNNINGHAM, Julie M; SELLERS, Thomas A; PANKRATZ, V. Shane et al.Cancer epidemiology, biomarkers & prevention. 2008, Vol 17, Num 7, pp 1781-1789, issn 1055-9965, 9 p.Article

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Strong evidence of a genetic determinant for mammographic density, a major risk factor for breast cancerVACHON, Celine M; SELLERS, Thomas A; CARLSON, Erin E et al.Cancer research (Baltimore). 2007, Vol 67, Num 17, pp 8412-8418, issn 0008-5472, 7 p.Article

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Analysis of the RNASEL gene in familial and sporadic prostate cancerLIANG WANG; MCDONNELL, Shannon K; BLUTE, Michael L et al.American journal of human genetics. 2002, Vol 71, Num 1, pp 116-123, issn 0002-9297Article

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomasCUNNINGHAM, Julie M; KIM, Cheong-Yong; KUBLY, Vickie et al.American journal of human genetics. 2001, Vol 69, Num 4, pp 780-790, issn 0002-9297Article

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Mapping of the IRF8 Gene Identifies a 3'UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma SubtypesSLAGER, Susan L; ACHENBACH, Sara J; WANG, Alice H et al.Cancer epidemiology, biomarkers & prevention. 2013, Vol 22, Num 3, pp 461-466, issn 1055-9965, 6 p.Article

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Nucleotide Excision Repair Pathway Polymorphisms and Pancreatic Cancer Risk: Evidence for role of MMS19LMCWILLIAMS, Robert R; BAMLET, William R; DE ANDRADE, Mariza et al.Cancer epidemiology, biomarkers & prevention. 2009, Vol 18, Num 4, pp 1295-1302, issn 1055-9965, 8 p.Article

Single Nucleotide Polymorphisms in the TP53 Region and Susceptibility to Invasive Epithelial Ovarian CancerSCHILDKRAUT, Joellen M; GOODE, Ellen L; CUNNINGHAM, Julie M et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 6, pp 2349-2357, issn 0008-5472, 9 p.Article

Coffee, Caffeine-Related Genes, and Parkinson's Disease : A Case-Control StudyFACHERIS, Maurizio F; SCHNEIDER, Nicole K; LESNICK, Timothy G et al.Movement disorders. 2008, Vol 23, Num 14, pp 2033-2040, issn 0885-3185, 8 p.Article

Two common chromosome 8q24 variants are associated with increased risk for prostate cancer. CommentaryPLATZ, Elizabeth A; LIANG WANG; THIBODEAU, Stephen N et al.Cancer research (Baltimore). 2007, Vol 67, Num 7, issn 0008-5472, 2905-2907,2944-2950 [10 p.]Article

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Androgen receptor gene polymorphisms and increased risk of urologic measures of benign prostatic hyperplasiaROBERTS, Rosebud O; BERGSTRALH, Erik J; CUNNINGHAM, Julie M et al.American journal of epidemiology. 2004, Vol 159, Num 3, pp 269-276, issn 0002-9262, 8 p.Article

Mutations in CHEK2 associated with prostate cancer riskXIANGYANG DONG; LIANG WANG; SMITH, David I et al.American journal of human genetics. 2003, Vol 72, Num 2, pp 270-280, issn 0002-9297, 11 p.Article