Lowstuter KJ - Search Results

1

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

2

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

3

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

4

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

5

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

6

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.

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

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

9

Psychosocial outcomes following germline multigene panel testing in an ethnically and economically diverse cohort of patients.

Culver JO, Ricker CN, Bonner J, Kidd J, Sturgeon D, Hodan R, Kingham K, Lowstuter K, Chun NM, Lebensohn AP, Rowe-Teeter C, Levonian P, Partynski K, Lara-Otero K, Hong C, Morales Pichardo J, Mills MA, Brown K, Lerman C, Ladabaum U, McDonnell KJ, Ford JM, Gruber SB, Kurian AW, Idos GE. Culver JO, et al. Among authors: lowstuter k. Cancer. 2021 Apr 15;127(8):1275-1285. doi: 10.1002/cncr.33357. Epub 2020 Dec 15. Cancer. 2021. PMID: 33320347 Free PMC article.

10

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.

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