Petrucelli N - Search Results

1

Racial and ethnic variation in multigene panel testing in a cohort of BRCA1/2-negative individuals who had genetic testing in a large urban comprehensive cancer center.

Tatineni S, Tarockoff M, Abdallah N, Purrington KS, Assad H, Reagle R, Petrucelli N, Simon MS. Tatineni S, et al. Among authors: petrucelli n. Cancer Med. 2022 Mar;11(6):1465-1473. doi: 10.1002/cam4.4541. Epub 2022 Jan 17. Cancer Med. 2022. PMID: 35040284 Free PMC article.

2

Hereditary breast and ovarian cancer syndrome : the impact of race on uptake of genetic counseling and testing.

Simon MS, Petrucelli N. Simon MS, et al. Among authors: petrucelli n. Methods Mol Biol. 2009;471:487-500. doi: 10.1007/978-1-59745-416-2_25. Methods Mol Biol. 2009. PMID: 19109796

3

Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2.

Petrucelli N, Daly MB, Feldman GL. Petrucelli N, et al. Genet Med. 2010 May;12(5):245-59. doi: 10.1097/GIM.0b013e3181d38f2f. Genet Med. 2010. PMID: 20216074 Free article. Review.

4

Variants in the Signaling Protein TSAd are Associated with Susceptibility to Ovarian Cancer in BRCA1/2 Negative High Risk Families.

Kaplun L, Fridman AL, Chen W, Levin NK, Ahsan S, Petrucelli N, Barrick JL, Gold R, Land S, Simon MS, Morris RT, Munkarah AR, Tainsky MA. Kaplun L, et al. Among authors: petrucelli n. Biomark Insights. 2012;7:151-7. doi: 10.4137/BMI.S10815. Epub 2012 Dec 12. Biomark Insights. 2012. PMID: 23300341 Free PMC article.

5

Prospective analysis of association between statin use and breast cancer risk in the women's health initiative.

Desai P, Chlebowski R, Cauley JA, Manson JE, Wu C, Martin LW, Jay A, Bock C, Cote M, Petrucelli N, Rosenberg CA, Peters U, Agalliu I, Budrys N, Abdul-Hussein M, Lane D, Luo J, Park HL, Thomas F, Wactawski-Wende J, Simon MS. Desai P, et al. Among authors: petrucelli n. Cancer Epidemiol Biomarkers Prev. 2013 Oct;22(10):1868-76. doi: 10.1158/1055-9965.EPI-13-0562. Epub 2013 Aug 23. Cancer Epidemiol Biomarkers Prev. 2013. PMID: 23975947 Free PMC article.

6

To reflex or not: additional BRCA1/2 testing in Ashkenazi Jewish individuals without founder mutations.

Petrucelli N, Mange S, Fulbright JL, Dohany L, Zakalik D, Duquette D. Petrucelli N, et al. J Genet Couns. 2015 Apr;24(2):285-93. doi: 10.1007/s10897-014-9762-z. Epub 2014 Sep 9. J Genet Couns. 2015. PMID: 25199548

7

Familial clustering of breast and prostate cancer and risk of postmenopausal breast cancer in the Women's Health Initiative Study.

Beebe-Dimmer JL, Yee C, Cote ML, Petrucelli N, Palmer N, Bock C, Lane D, Agalliu I, Stefanick ML, Simon MS. Beebe-Dimmer JL, et al. Among authors: petrucelli n. Cancer. 2015 Apr 15;121(8):1265-72. doi: 10.1002/cncr.29075. Epub 2015 Mar 9. Cancer. 2015. PMID: 25754547 Free PMC article.

8

Large, Prospective Analysis of the Reasons Patients Do Not Pursue BRCA Genetic Testing Following Genetic Counseling.

Hayden S, Mange S, Duquette D, Petrucelli N, Raymond VM; BRCA Clinical Network Partners. Hayden S, et al. Among authors: petrucelli n. J Genet Couns. 2017 Aug;26(4):859-865. doi: 10.1007/s10897-016-0064-5. Epub 2017 Jan 16. J Genet Couns. 2017. PMID: 28093663 Free article.

9

Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability.

Stafford JL, Dyson G, Levin NK, Chaudhry S, Rosati R, Kalpage H, Wernette C, Petrucelli N, Simon MS, Tainsky MA. Stafford JL, et al. Among authors: petrucelli n. PLoS One. 2017 Jun 7;12(6):e0178450. doi: 10.1371/journal.pone.0178450. eCollection 2017. PLoS One. 2017. PMID: 28591191 Free PMC article.

10

Cell-free DNA results lead to unexpected diagnosis.

Smith J, Kean V, Bianchi DW, Feldman G, Petrucelli N, Simon M, Gonik B. Smith J, et al. Among authors: petrucelli n. Clin Case Rep. 2017 Jul 3;5(8):1323-1326. doi: 10.1002/ccr3.1051. eCollection 2017 Aug. Clin Case Rep. 2017. PMID: 28781851 Free PMC article.

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