Weitzel JN - 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. 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

The HRAS1 minisatellite locus and risk of ovarian cancer.

Weitzel JN, Ding S, Larson GP, Nelson RA, Goodman A, Grendys EC, Ball HG, Krontiris TG. Weitzel JN, et al. Cancer Res. 2000 Jan 15;60(2):259-61. Cancer Res. 2000. PMID: 10667571

3

Restriction endonuclease fingerprinting enhanced conformation sensitive gel electrophoresis (REF-CSGE) in the analysis of BRCA1 exon 11 mutations in a high-risk breast cancer cohort.

Herzog JS, Jancis EM, Liao S, Somlo G, Weitzel JN. Herzog JS, et al. Among authors: weitzel jn. Hum Mutat. 2002 Jun;19(6):656-63. doi: 10.1002/humu.10091. Hum Mutat. 2002. PMID: 12007222

4

Development of a cancer genetics education program for clinicians.

Blazer KR, Grant M, Sand SR, MacDonald DJ, Choi JJ, Nedelcu RA, Weitzel JN. Blazer KR, et al. Among authors: weitzel jn. J Cancer Educ. 2002 Summer;17(2):69-73. doi: 10.1080/08858190209528801. J Cancer Educ. 2002. PMID: 12092855

5

Effect of genetic cancer risk assessment on surgical decisions at breast cancer diagnosis.

Weitzel JN, McCaffrey SM, Nedelcu R, MacDonald DJ, Blazer KR, Cullinane CA. Weitzel JN, et al. Arch Surg. 2003 Dec;138(12):1323-8; discussion 1329. doi: 10.1001/archsurg.138.12.1323. Arch Surg. 2003. PMID: 14662532

6

Outcomes from intensive training in genetic cancer risk counseling for clinicians.

Blazer KR, MacDonald DJ, Ricker C, Sand S, Uman GC, Weitzel JN. Blazer KR, et al. Among authors: weitzel jn. Genet Med. 2005 Jan;7(1):40-7. doi: 10.1097/01.gim.0000151154.27612.49. Genet Med. 2005. PMID: 15654227

7

Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers.

Cullinane CA, Lubinski J, Neuhausen SL, Ghadirian P, Lynch HT, Isaacs C, Weber B, Moller P, Offit K, Kim-Sing C, Friedman E, Randall S, Pasini B, Ainsworth P, Gershoni-Baruch R, Foulkes WD, Klijn J, Tung N, Rennert G, Olopade O, Couch F, Wagner T, Olsson H, Sun P, Weitzel JN, Narod SA. Cullinane CA, et al. Among authors: weitzel jn. Int J Cancer. 2005 Dec 20;117(6):988-91. doi: 10.1002/ijc.21273. Int J Cancer. 2005. PMID: 15986445

8

Prevalence of BRCA mutations and founder effect in high-risk Hispanic families.

Weitzel JN, Lagos V, Blazer KR, Nelson R, Ricker C, Herzog J, McGuire C, Neuhausen S. Weitzel JN, et al. Cancer Epidemiol Biomarkers Prev. 2005 Jul;14(7):1666-71. doi: 10.1158/1055-9965.EPI-05-0072. Cancer Epidemiol Biomarkers Prev. 2005. PMID: 16030099

9

Linkage of a pedigree drawing program and database to a program for determining BRCA mutation carrier probability.

Sand SR, DeRam DS, MacDonald DJ, Blazer KR, Weitzel JN. Sand SR, et al. Among authors: weitzel jn. Fam Cancer. 2005;4(4):313-6. doi: 10.1007/s10689-005-8849-y. Fam Cancer. 2005. PMID: 16341809

10

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

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

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