Shirts BH - Search Results

1

Incorporating user feedback in the design of a genetics analysis tool: A two-part approach.

Swaminathan A, Shirts BH, Chen AT. Swaminathan A, et al. Among authors: shirts bh. J Biomed Inform. 2019 Jul;95:103204. doi: 10.1016/j.jbi.2019.103204. Epub 2019 May 7. J Biomed Inform. 2019. PMID: 31075532 Free article.

2

The genomic CDS sandbox: An assessment among domain experts.

Aziz A, Kawamoto K, Eilbeck K, Williams MS, Freimuth RR, Hoffman MA, Rasmussen LV, Overby CL, Shirts BH, Hoffman JM, Welch BM. Aziz A, et al. Among authors: shirts bh. J Biomed Inform. 2016 Apr;60:84-94. doi: 10.1016/j.jbi.2015.12.019. Epub 2016 Jan 15. J Biomed Inform. 2016. PMID: 26778834 Free PMC article.

3

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. Among authors: shirts bh. 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.

4

Exploring relatives' perceptions of participation, ethics, and communication in a patient-driven study for hereditary cancer variant reclassification.

Tsai GJ, Chen AT, Garrett LT, Burke W, Bowen DJ, Shirts BH. Tsai GJ, et al. Among authors: shirts bh. J Genet Couns. 2020 Oct;29(5):857-866. doi: 10.1002/jgc4.1215. Epub 2020 Jan 9. J Genet Couns. 2020. PMID: 31916645 Free PMC article.

5

An algorithm for optimal testing in co-segregation analysis.

Buie RW, Rañola JMO, Chen AT, Shirts BH. Buie RW, et al. Among authors: shirts bh. Hum Mutat. 2022 May;43(5):547-556. doi: 10.1002/humu.24363. Epub 2022 Apr 7. Hum Mutat. 2022. PMID: 35225377 Free PMC article.

6

Diagnostic yield of genetic screening in a diverse, community-ascertained cohort.

Rao ND, Kaganovsky J, Malouf EA, Coe S, Huey J, Tsinajinne D, Hassan S, King KM, Fullerton SM, Chen AT, Shirts BH. Rao ND, et al. Among authors: shirts bh. Genome Med. 2023 Apr 18;15(1):26. doi: 10.1186/s13073-023-01174-7. Genome Med. 2023. PMID: 37069702 Free PMC article.

7

Extended Family Outreach in Hereditary Cancer Using Web-Based Genealogy, Direct-to-Consumer Ancestry Genetics, and Social Media: Mixed Methods Process Evaluation of the ConnectMyVariant Intervention.

Chen AT, Huey J, Coe S, Kaganovsky J, Malouf EA, Evans HD, Daker J, Harper E, Fordiani O, Lowe EE, Oldroyd CM, Price A, Roth K, Stoddard J, Crandell JN, Shirts BH. Chen AT, et al. Among authors: shirts bh. JMIR Cancer. 2023 Apr 20;9:e43126. doi: 10.2196/43126. JMIR Cancer. 2023. PMID: 37079361 Free PMC article.

8

Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients.

Rao ND, King KM, Kaganovsky J, Hassan S, Tsinajinne D, Fullerton SM, Chen AT, Veenstra DL, Shirts BH. Rao ND, et al. Among authors: shirts bh. Eur J Hum Genet. 2024 Jan;32(1):77-82. doi: 10.1038/s41431-023-01460-3. Epub 2023 Sep 26. Eur J Hum Genet. 2024. PMID: 37752309

9

Family-Specific Variants and the Limits of Human Genetics.

Shirts BH, Pritchard CC, Walsh T. Shirts BH, et al. Trends Mol Med. 2016 Nov;22(11):925-934. doi: 10.1016/j.molmed.2016.09.007. Epub 2016 Oct 11. Trends Mol Med. 2016. PMID: 27742414 Free PMC article. Review.

10

A comparison of cosegregation analysis methods for the clinical setting.

Rañola JMO, Liu Q, Rosenthal EA, Shirts BH. Rañola JMO, et al. Among authors: shirts bh. Fam Cancer. 2018 Apr;17(2):295-302. doi: 10.1007/s10689-017-0017-7. Fam Cancer. 2018. PMID: 28695303 Free PMC article.

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