Milliron KJ - Search Results

1

Absence of CHEK2*1100delC mutation in families with hereditary breast cancer in North America.

Iniesta MD, Gorin MA, Chien LC, Thomas SM, Milliron KJ, Douglas JA, Merajver SD. Iniesta MD, et al. Among authors: milliron kj. Cancer Genet Cytogenet. 2010 Oct 15;202(2):136-40. doi: 10.1016/j.cancergencyto.2010.07.124. Cancer Genet Cytogenet. 2010. PMID: 20875877

2

BRCA-associated cancer risk: molecular biology and clinical practice.

van Golen K, Milliron K, Davies S, Merajver SD. van Golen K, et al. J Lab Clin Med. 1999 Jul;134(1):11-8. doi: 10.1016/s0022-2143(99)90049-5. J Lab Clin Med. 1999. PMID: 10402055 Review. No abstract available.

3

Cancer-specific worry interference in women attending a breast and ovarian cancer risk evaluation program: impact on emotional distress and health functioning.

Trask PC, Paterson AG, Wang C, Hayasaka S, Milliron KJ, Blumberg LR, Gonzalez R, Murray S, Merajver SD. Trask PC, et al. Among authors: milliron kj. Psychooncology. 2001 Sep-Oct;10(5):349-60. doi: 10.1002/pon.510. Psychooncology. 2001. PMID: 11536413 Free article.

4

Health insurance and discrimination concerns and BRCA1/2 testing in a clinic population.

Peterson EA, Milliron KJ, Lewis KE, Goold SD, Merajver SD. Peterson EA, et al. Among authors: milliron kj. Cancer Epidemiol Biomarkers Prev. 2002 Jan;11(1):79-87. Cancer Epidemiol Biomarkers Prev. 2002. PMID: 11815404

5

Genetic counseling for BRCA1/2: a randomized controlled trial of two strategies to facilitate the education and counseling process.

Wang C, Gonzalez R, Milliron KJ, Strecher VJ, Merajver SD. Wang C, et al. Among authors: milliron kj. Am J Med Genet A. 2005 Apr 1;134A(1):66-73. doi: 10.1002/ajmg.a.30577. Am J Med Genet A. 2005. PMID: 15690408 Free article. Clinical Trial.

6

Breast cancer risk assessment: a guide for clinicians using the NCCN Breast Cancer Risk Reduction Guidelines.

Merajver SD, Milliron K. Merajver SD, et al. J Natl Compr Canc Netw. 2003 Apr;1(2):297-301. doi: 10.6004/jnccn.2003.0027. J Natl Compr Canc Netw. 2003. PMID: 19768887

7

Differences between women who pursued genetic testing for hereditary breast and ovarian cancer and their at-risk relatives who did not.

Katapodi MC, Northouse L, Pierce P, Milliron KJ, Liu G, Merajver SD. Katapodi MC, et al. Among authors: milliron kj. Oncol Nurs Forum. 2011 Sep;38(5):572-81. doi: 10.1188/11.ONF.572-581. Oncol Nurs Forum. 2011. PMID: 21875844

8

Individual and family characteristics associated with BRCA1/2 genetic testing in high-risk families.

Katapodi MC, Northouse LL, Milliron KJ, Liu G, Merajver SD. Katapodi MC, et al. Among authors: milliron kj. Psychooncology. 2013 Jun;22(6):1336-43. doi: 10.1002/pon.3139. Epub 2012 Jul 24. Psychooncology. 2013. PMID: 22826208 Free article.

9

Using a state cancer registry to recruit young breast cancer survivors and high-risk relatives: protocol of a randomized trial testing the efficacy of a targeted versus a tailored intervention to increase breast cancer screening.

Katapodi MC, Northouse LL, Schafenacker AM, Duquette D, Duffy SA, Ronis DL, Anderson B, Janz NK, McLosky J, Milliron KJ, Merajver SD, Duong LM, Copeland G. Katapodi MC, et al. Among authors: milliron kj. BMC Cancer. 2013 Mar 1;13:97. doi: 10.1186/1471-2407-13-97. BMC Cancer. 2013. PMID: 23448100 Free PMC article. Clinical Trial.

10

Use of Cancer Genetics Services in African-American Young Breast Cancer Survivors.

Jones T, Lockhart JS, Mendelsohn-Victor KE, Duquette D, Northouse LL, Duffy SA, Donley R, Merajver SD, Milliron KJ, Roberts JS, Katapodi MC. Jones T, et al. Among authors: milliron kj. Am J Prev Med. 2016 Oct;51(4):427-36. doi: 10.1016/j.amepre.2016.03.016. Epub 2016 Apr 23. Am J Prev Med. 2016. PMID: 27117712

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