Shirts B - Search Results

1

Socioeconomic Status and Interest in Genetic Testing in a US-Based Sample.

Dusic EJ, Bowen DJ, Bennett R, Cain KC, Theoryn T, Velasquez M, Swisher E, Brant JM, Shirts B, Wang C. Dusic EJ, et al. Among authors: shirts b. Healthcare (Basel). 2022 May 10;10(5):880. doi: 10.3390/healthcare10050880. Healthcare (Basel). 2022. PMID: 35628017 Free PMC article.

2

Actionable, pathogenic incidental findings in 1,000 participants' exomes.

Dorschner MO, Amendola LM, Turner EH, Robertson PD, Shirts BH, Gallego CJ, Bennett RL, Jones KL, Tokita MJ, Bennett JT, Kim JH, Rosenthal EA, Kim DS; National Heart, Lung, and Blood Institute Grand Opportunity Exome Sequencing Project; Tabor HK, Bamshad MJ, Motulsky AG, Scott CR, Pritchard CC, Walsh T, Burke W, Raskind WH, Byers P, Hisama FM, Nickerson DA, Jarvik GP. Dorschner MO, et al. Am J Hum Genet. 2013 Oct 3;93(4):631-40. doi: 10.1016/j.ajhg.2013.08.006. Epub 2013 Sep 19. Am J Hum Genet. 2013. PMID: 24055113 Free PMC article.

3

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. 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

4

Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational Tool.

Garrett LT, Hickman N, Jacobson A, Bennett RL, Amendola LM, Rosenthal EA, Shirts BH. Garrett LT, et al. J Genet Couns. 2016 Dec;25(6):1146-1156. doi: 10.1007/s10897-016-9993-2. Epub 2016 Jul 16. J Genet Couns. 2016. PMID: 27422780 Free PMC article.

5

Hereditary cancer gene panel test reports: wide heterogeneity suggests need for standardization.

Makhnoon S, Shirts BH, Bowen DJ, Fullerton SM. Makhnoon S, et al. Genet Med. 2018 Nov;20(11):1438-1445. doi: 10.1038/gim.2018.23. Epub 2018 Mar 1. Genet Med. 2018. PMID: 29493582 Free article.

6

Experiences of patients seeking to participate in variant of uncertain significance reclassification research.

Makhnoon S, Garrett LT, Burke W, Bowen DJ, Shirts BH. Makhnoon S, et al. J Community Genet. 2019 Apr;10(2):189-196. doi: 10.1007/s12687-018-0375-3. Epub 2018 Jul 19. J Community Genet. 2019. PMID: 30027524 Free PMC article.

7

Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance.

Tsai GJ, Rañola JMO, Smith C, Garrett LT, Bergquist T, Casadei S, Bowen DJ, Shirts BH. Tsai GJ, et al. Genet Med. 2019 Jun;21(6):1435-1442. doi: 10.1038/s41436-018-0335-7. Epub 2018 Oct 30. Genet Med. 2019. PMID: 30374176 Free article.

8

Patients' perspectives of variants of uncertain significance and strategies for uncertainty management.

Makhnoon S, Shirts BH, Bowen DJ. Makhnoon S, et al. J Genet Couns. 2019 Apr;28(2):313-325. doi: 10.1002/jgc4.1075. Epub 2019 Jan 12. J Genet Couns. 2019. PMID: 30636062

9

Patient goals, motivations, and attitudes in a patient-driven variant reclassification study.

Tsai GJ, Garrett LT, Makhnoon S, Bowen DJ, Burke W, Shirts BH. Tsai GJ, et al. J Genet Couns. 2019 Jun;28(3):558-569. doi: 10.1002/jgc4.1052. Epub 2018 Dec 31. J Genet Couns. 2019. PMID: 31163102

10

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: shirts b. 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.

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