Lowstuter KJ - Search Results

1

Influence of genetic discrimination perceptions and knowledge on cancer genetics referral practice among clinicians.

Lowstuter KJ, Sand S, Blazer KR, MacDonald DJ, Banks KC, Lee CA, Schwerin BU, Juarez M, Uman GC, Weitzel JN. Lowstuter KJ, et al. Genet Med. 2008 Sep;10(9):691-8. doi: 10.1097/gim.0b013e3181837246. Genet Med. 2008. PMID: 18978681 Free article.

2

Evolving perspectives on genetic discrimination in health insurance among health care providers.

Huizenga CR, Lowstuter K, Banks KC, Lagos VI, Vandergon VO, Weitzel JN. Huizenga CR, et al. Fam Cancer. 2010 Jun;9(2):253-60. doi: 10.1007/s10689-009-9308-y. Fam Cancer. 2010. PMID: 19967457

3

Limited family structure and BRCA gene mutation status in single cases of breast cancer.

Weitzel JN, Lagos VI, Cullinane CA, Gambol PJ, Culver JO, Blazer KR, Palomares MR, Lowstuter KJ, MacDonald DJ. Weitzel JN, et al. Among authors: lowstuter kj. JAMA. 2007 Jun 20;297(23):2587-95. doi: 10.1001/jama.297.23.2587. JAMA. 2007. PMID: 17579227

4

If we build it ... will they come?--establishing a cancer genetics services clinic for an underserved predominantly Latina cohort.

Ricker C, Lagos V, Feldman N, Hiyama S, Fuentes S, Kumar V, Gonzalez K, Palomares M, Blazer K, Lowstuter K, MacDonald D, Weitzel J. Ricker C, et al. J Genet Couns. 2006 Dec;15(6):505-14. doi: 10.1007/s10897-006-9052-5. J Genet Couns. 2006. PMID: 17106633

5

Breast cancer and the family tree. An issue for all practice settings.

Edwards QT, Seibert D, Maradiegue A, MacDonald D, Jasperson K, Lowstuter K, Weitzel J. Edwards QT, et al. Adv Nurse Pract. 2007 May;15(5):34-41; quiz 41-2. Adv Nurse Pract. 2007. PMID: 20000211 No abstract available.

6

Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families.

Weitzel JN, Lagos VI, Herzog JS, Judkins T, Hendrickson B, Ho JS, Ricker CN, Lowstuter KJ, Blazer KR, Tomlinson G, Scholl T. Weitzel JN, et al. Among authors: lowstuter kj. Cancer Epidemiol Biomarkers Prev. 2007 Aug;16(8):1615-20. doi: 10.1158/1055-9965.EPI-07-0198. Epub 2007 Jul 23. Cancer Epidemiol Biomarkers Prev. 2007. PMID: 17646271

7

Assessing the predictive accuracy of hMLH1 and hMSH2 mutation probability models.

Jasperson KW, Lowstuter K, Weitzel JN. Jasperson KW, et al. J Genet Couns. 2006 Oct;15(5):339-47. doi: 10.1007/s10897-006-9035-6. J Genet Couns. 2006. PMID: 16969708

8

Working through a diagnostic challenge: colonic polyposis, Amsterdam criteria, and a mismatch repair mutation.

Jasperson KW, Blazer KR, Lowstuter K, Weitzel JN. Jasperson KW, et al. Fam Cancer. 2008;7(4):281-5. doi: 10.1007/s10689-007-9179-z. Epub 2008 Jan 6. Fam Cancer. 2008. PMID: 18176851

9

Scoping the family history: assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings--a primer for nurse practitioners.

Maradiegue A, Jasperson K, Edwards QT, Lowstuter K, Weitzel J. Maradiegue A, et al. J Am Acad Nurse Pract. 2008 Feb;20(2):76-84. doi: 10.1111/j.1745-7599.2007.00282.x. J Am Acad Nurse Pract. 2008. PMID: 18271762 Review.

10

Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations.

Gonzalez KD, Noltner KA, Buzin CH, Gu D, Wen-Fong CY, Nguyen VQ, Han JH, Lowstuter K, Longmate J, Sommer SS, Weitzel JN. Gonzalez KD, et al. J Clin Oncol. 2009 Mar 10;27(8):1250-6. doi: 10.1200/JCO.2008.16.6959. Epub 2009 Feb 9. J Clin Oncol. 2009. PMID: 19204208

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