Bennett RL - Search Results

1

Germline mutation in MSH6 associated with multiple malignant neoplasms in a patient With Muir-Torre syndrome.

Tavakkol Z, Keller JJ, Furmanczyk PS, Bennett RL, Chien AJ. Tavakkol Z, et al. Among authors: bennett rl. J Clin Oncol. 2012 Aug 1;30(22):e195-8. doi: 10.1200/JCO.2011.41.5562. Epub 2012 Jun 25. J Clin Oncol. 2012. PMID: 22734033 No abstract available.

2

A mosaic PTEN mutation causing Cowden syndrome identified by deep sequencing.

Pritchard CC, Smith C, Marushchak T, Koehler K, Holmes H, Raskind W, Walsh T, Bennett RL. Pritchard CC, et al. Among authors: bennett rl. Genet Med. 2013 Dec;15(12):1004-7. doi: 10.1038/gim.2013.51. Epub 2013 Apr 25. Genet Med. 2013. PMID: 23619277 Free article.

3

Biochemical and imaging surveillance in Li-Fraumeni syndrome.

Raskind WH, Hisama FM, Bennett RL. Raskind WH, et al. Among authors: bennett rl. Lancet Oncol. 2016 Nov;17(11):e472. doi: 10.1016/S1470-2045(16)30530-7. Lancet Oncol. 2016. PMID: 27819239 No abstract available.

4

Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests.

Amendola LM, Hart MR, Bennett RL, Horike-Pyne M, Dorschner M, Shirts B, Jarvik GP. Amendola LM, et al. Among authors: bennett rl. J Genet Couns. 2019 Dec;28(6):1208-1213. doi: 10.1002/jgc4.1155. Epub 2019 Jul 17. J Genet Couns. 2019. PMID: 31317629 Free PMC article.

5

Simultaneous germline and somatic sequencing in ovarian carcinoma: mutation rate and impact on clinical decision-making.

Jorge S, McFaddin AS, Doll KM, Pennington KP, Norquist BM, Bennett RL, Pritchard CC, Swisher EM. Jorge S, et al. Among authors: bennett rl. Gynecol Oncol. 2020 Mar;156(3):517-522. doi: 10.1016/j.ygyno.2019.12.010. Epub 2019 Dec 27. Gynecol Oncol. 2020. PMID: 31883735

6

A self-administered family history questionnaire improves identification of women who warrant referral to genetic counseling for hereditary cancer risk.

Vogel TJ, Stoops K, Bennett RL, Miller M, Swisher EM. Vogel TJ, et al. Among authors: bennett rl. Gynecol Oncol. 2012 Jun;125(3):693-8. doi: 10.1016/j.ygyno.2012.03.025. Epub 2012 Mar 21. Gynecol Oncol. 2012. PMID: 22446623

7

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.

Pritchard CC, Smith C, Salipante SJ, Lee MK, Thornton AM, Nord AS, Gulden C, Kupfer SS, Swisher EM, Bennett RL, Novetsky AP, Jarvik GP, Olopade OI, Goodfellow PJ, King MC, Tait JF, Walsh T. Pritchard CC, et al. Among authors: bennett rl. J Mol Diagn. 2012 Jul;14(4):357-66. doi: 10.1016/j.jmoldx.2012.03.002. Epub 2012 May 30. J Mol Diagn. 2012. PMID: 22658618 Free PMC article.

8

Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.

Murray ML, Cerrato F, Bennett RL, Jarvik GP. Murray ML, et al. Among authors: bennett rl. Genet Med. 2011 Dec;13(12):998-1005. doi: 10.1097/GIM.0b013e318226fc15. Genet Med. 2011. PMID: 21811163 Free article.

9

Recommendations for returning genomic incidental findings? We need to talk!

Burke W, Antommaria AH, Bennett R, Botkin J, Clayton EW, Henderson GE, Holm IA, Jarvik GP, Khoury MJ, Knoppers BM, Press NA, Ross LF, Rothstein MA, Saal H, Uhlmann WR, Wilfond B, Wolf SM, Zimmern R. Burke W, et al. Genet Med. 2013 Nov;15(11):854-9. doi: 10.1038/gim.2013.113. Epub 2013 Aug 1. Genet Med. 2013. PMID: 23907645 Free PMC article. Review.

10

Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome.

Gallego CJ, Perez ML, Burt A, Amendola LM, Shirts BH, Pritchard CC, Hisama FM, Bennett RL, Veenstra DL, Jarvik GP. Gallego CJ, et al. Among authors: bennett rl. J Genet Couns. 2016 Jun;25(3):515-9. doi: 10.1007/s10897-015-9902-0. Epub 2015 Dec 5. J Genet Couns. 2016. PMID: 26637299

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