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Prevention and Treatment Publications

Shah FT, French KS, Osann KE, Bocian M, Jones MC, Korty L. Impact of cell-free fetal DNA screening patients' choice of invasive procedures after a positive California prenatal screen result. J Clin Med 2014, 3(3), 849-864.

Weitzel J, Claque J, Martir-Negron A, Ogaz R, Herzog J, Ricker C, Jungbluth C, Cina C, e al. Prevalence and type of BRCA mutations in hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network. J of Clin Oncol. 2013 May 1;31(13):1702.

Brown SM, Culver JO, Osann KE, MacDonald DJ, Sand S, Thornton AA, Grant M, Bowen DJ, Metcalfe KA, Burke HB, Robson ME, Friedman S, Weitzel JN Health literacy, numeracy, and interpretation of graphical breast cancer risk estimates. Patient Educ Coun. 2011 Apr;83(1):92-8.

Huizenga CR, Lowstuter K, Banks KC, Lagos VI, Vandergon VO, Weitzel JN. Evolving perspectives on genetic discrimination in health insurance among health care providers. Fam Cancer 2010 Jun;9(2):253-60.

McKinnon W, Banks KC, Skelly J, Kohlman W , Bennett R, Shannon K, Larson-Haidle J, Ashakaga T, Weitzel JN, Wood M. Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals. Fam Cancer. 2009;8(4):363-9.

Leachman S, Carucci J, Kohlmann W, Banks KC, Asgari M, Bergman W, et al. Selection criteria for genetic assessment of patients with familial melanoma. J Am Acad Dermatol. 2009 Oct;61(4):677.

Lowstuter KJ, Sand S, Blazer KR, MacDonald DJ, Banks KC, Lee CA, Schwerin BU, Juarez M, Uman GC, Weitzel JN. Influence of genetic discrimination perceptions and knowledge on cancer genetics referral practice among clinicians. Genet Med. 2008 Sep;10(9):691-8.

Tuazon E, Banks K, Koh CJ, De Filippo RE, Chang A, Hardy BE, Cortessis VK. Prepubertal orchiopexy for cryptorchidism may be associated with lower risk of testicular cancer. J Urol. 2008 Aug;180(2):783-4.

Weitzel JN, Lagos V, Blazer KR, Nelson R, Ricker C, Herzog J, McGuire C, Neuhausen S. Prevalence of BRCA mutations and founder effect in high-risk Hispanic families. Cancer Epidemiol Biomarkers Prev. 2005 Jul;14(7):1666-71.