Stanislaw C - Search Results

1

Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™).

Bellcross C, Hermstad A, Tallo C, Stanislaw C. Bellcross C, et al. Among authors: stanislaw c. Genet Med. 2019 Jan;21(1):181-184. doi: 10.1038/s41436-018-0020-x. Epub 2018 May 8. Genet Med. 2019. PMID: 29740170 Free article.

2

Impact of Implementing B-RST^TM to Screen for Hereditary Breast and Ovarian Cancer on Risk Perception and Genetic Counseling Uptake Among Women in an Academic Safety Net Hospital.

Wernke K, Bellcross C, Gabram S, Ali N, Stanislaw C. Wernke K, et al. Among authors: stanislaw c. Clin Breast Cancer. 2019 Aug;19(4):e547-e555. doi: 10.1016/j.clbc.2019.02.014. Epub 2019 Mar 11. Clin Breast Cancer. 2019. PMID: 31005475

3

Validation of the pedigree assessment tool (PAT) in families with BRCA1 and BRCA2 mutations.

Teller P, Hoskins KF, Zwaagstra A, Stanislaw C, Iyengar R, Green VL, Gabram SG. Teller P, et al. Among authors: stanislaw c. Ann Surg Oncol. 2010 Jan;17(1):240-6. doi: 10.1245/s10434-009-0697-9. Epub 2009 Sep 18. Ann Surg Oncol. 2010. PMID: 19763692

4

Prevention and Screening in Hereditary Breast and Ovarian Cancer.

Zeichner SB, Stanislaw C, Meisel JL. Zeichner SB, et al. Among authors: stanislaw c. Oncology (Williston Park). 2016 Oct 15;30(10):896-904. Oncology (Williston Park). 2016. PMID: 27753056 Free article. Review.

5

Evaluating the Effectiveness of a Telehealth Cancer Genetics Program: A BRCA Pilot Study.

Rose E, Hardy MW, Gates R, Stanislaw C, Meisel J, Grinzaid KA. Rose E, et al. Among authors: stanislaw c. Public Health Genomics. 2022 Aug 9:1-14. doi: 10.1159/000525658. Online ahead of print. Public Health Genomics. 2022. PMID: 35944511 Free article.

6

Presymptomatic ALS genetic counseling and testing: Experience and recommendations.

Benatar M, Stanislaw C, Reyes E, Hussain S, Cooley A, Fernandez MC, Dauphin DD, Michon SC, Andersen PM, Wuu J. Benatar M, et al. Among authors: stanislaw c. Neurology. 2016 Jun 14;86(24):2295-302. doi: 10.1212/WNL.0000000000002773. Epub 2016 May 18. Neurology. 2016. PMID: 27194384 Free PMC article. Review.

7

Adverse events in cancer genetic testing: the third case series.

Bonadies DC, Brierley KL, Barnett RE, Baxter MD, Donenberg T, Ducaine WL, Ernst ME, Homer J, Judkins M, Lovick NM, Powers JM, Stanislaw C, Stark E, Stenner RC, Matloff ET. Bonadies DC, et al. Among authors: stanislaw c. Cancer J. 2014 Jul-Aug;20(4):246-53. doi: 10.1097/PPO.0000000000000057. Cancer J. 2014. PMID: 25098283

8

Impact of presymptomatic genetic testing for familial amyotrophic lateral sclerosis.

Fanos JH, Gronka S, Wuu J, Stanislaw C, Andersen PM, Benatar M. Fanos JH, et al. Among authors: stanislaw c. Genet Med. 2011 Apr;13(4):342-8. doi: 10.1097/GIM.0b013e318204d004. Genet Med. 2011. PMID: 21285887 Free PMC article.

9

Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing.

Stanislaw C, Xue Y, Wilcox WR. Stanislaw C, et al. Cancer Biol Med. 2016 Mar;13(1):55-67. doi: 10.28092/j.issn.2095-3941.2016.0002. Cancer Biol Med. 2016. PMID: 27144062 Free PMC article.

10

Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications.

Brierley KL, Blouch E, Cogswell W, Homer JP, Pencarinha D, Stanislaw CL, Matloff ET. Brierley KL, et al. Cancer J. 2012 Jul-Aug;18(4):303-9. doi: 10.1097/PPO.0b013e3182609490. Cancer J. 2012. PMID: 22846730 Review.

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