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For: Hylind R, Smith M, Rasmussen-Torvik L, Aufox S. Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results. J Community Genet 2018;9:19-26. [PMID: 28656483 DOI: 10.1007/s12687-017-0314-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 14] [Article Influence: 2.2] [Reference Citation Analysis]
Number Citing Articles
1 Madrid SD, Blum-Barnett E, Lemke AA, Pan V, Paolino V, McGlynn EA, Burnett-Hartman AN. "A Gift to My Family for Their Future": Attitudes about Genetic Research Participation. Public Health Genomics 2022;:1-10. [PMID: 35545013 DOI: 10.1159/000524462] [Reference Citation Analysis]
2 Barlow-Stewart K, Bardsley K, Elan E, Fleming J, Berman Y, Fleischer R, Recsei K, Goldberg D, Tucker J, Burnett L. Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community. J Community Genet 2021. [PMID: 34846685 DOI: 10.1007/s12687-021-00567-8] [Reference Citation Analysis]
3 Vears DF, Minion JT, Roberts SJ, Cummings J, Machirori M, Blell M, Budin-Ljøsne I, Cowley L, Dyke SOM, Gaff C, Green R, Hall A, Johns AL, Knoppers BM, Mulrine S, Patch C, Winkler E, Murtagh MJ. Return of individual research results from genomic research: A systematic review of stakeholder perspectives. PLoS One 2021;16:e0258646. [PMID: 34748551 DOI: 10.1371/journal.pone.0258646] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
4 Swanson K, Sparks TN, Lianoglou BR, Chen F, Downum S, Patel S, Rego S, Yip T, Van Ziffle J, Koenig BA, Slavotinek AM, Norton ME. Preference for secondary findings in prenatal and pediatric exome sequencing. Prenat Diagn 2021. [PMID: 34057224 DOI: 10.1002/pd.5973] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
5 Vears DF, Minion JT, Roberts SJ, Cummings J, Machirori M, Murtagh MJ. Views on genomic research result delivery methods and informed consent: a review. Per Med 2021;18:295-310. [PMID: 33822658 DOI: 10.2217/pme-2020-0139] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
6 Gaille M, Horn R; UK-FR GENE (Genetics and Ethics Network) Consortia. The ethics of genomic medicine: redefining values and norms in the UK and France. Eur J Hum Genet 2021;29:780-8. [PMID: 33456054 DOI: 10.1038/s41431-020-00798-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
7 Etchegary H, Winsor M, Power A, Simmonds C. Public engagement with genomic medicine: a summary of town hall discussions. J Community Genet 2021;12:27-35. [PMID: 32865775 DOI: 10.1007/s12687-020-00485-1] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
8 Etchegary H, Wilson B, Rahman P, Simmonds C, Pullman D. Public interest in whole genome sequencing and information needs: an online survey study. Personalized Medicine 2020;17:283-93. [DOI: 10.2217/pme-2019-0136] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
9 Smit AK, Reyes-Marcelino G, Keogh L, Cust AE, Newson AJ. 'There is a lot of good in knowing, but there is also a lot of downs': public views on ethical considerations in population genomic screening. J Med Ethics 2020:medethics-2019-105934. [PMID: 32434901 DOI: 10.1136/medethics-2019-105934] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
10 Hao J, Hassen D, Manickam K, Murray MF, Hartzel DN, Hu Y, Liu K, Rahm AK, Williams MS, Lazzeri A, Buchanan A, Sturm A, Snyder SR. Healthcare Utilization and Costs after Receiving a Positive BRCA1/2 Result from a Genomic Screening Program. J Pers Med 2020;10:E7. [PMID: 32028596 DOI: 10.3390/jpm10010007] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
11 Horton R, Crawford G, Freeman L, Fenwick A, Wright CF, Lucassen A. Direct-to-consumer genetic testing. BMJ 2019;367:l5688. [PMID: 31619392 DOI: 10.1136/bmj.l5688] [Cited by in Crossref: 19] [Cited by in F6Publishing: 28] [Article Influence: 6.3] [Reference Citation Analysis]
12 Ballard LM, Horton RH, Fenwick A, Lucassen AM. Genome sequencing in healthcare: understanding the UK general public's views and implications for clinical practice. Eur J Hum Genet 2020;28:155-64. [PMID: 31527856 DOI: 10.1038/s41431-019-0504-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
13 Fleming J, Terrill B, Dziadek M, Kirk EP, Roscioli T, Barlow-stewart K. Personal genomic screening: How best to facilitate preparedness of future clients. European Journal of Medical Genetics 2019;62:397-404. [DOI: 10.1016/j.ejmg.2019.05.006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
14 Lu A, Kuhn P, Deichaite I. Time for a change: considering the rights of study participants to ownership of their personal research-grade genomic data. Converg Sci Phys Oncol 2018;4:046001. [DOI: 10.1088/2057-1739/aaf822] [Reference Citation Analysis]