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For: Brothers KB, Vassy JL, Green RC. Reconciling Opportunistic and Population Screening in Clinical Genomics. Mayo Clin Proc 2019;94:103-9. [PMID: 30611438 DOI: 10.1016/j.mayocp.2018.08.028] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 4.7] [Reference Citation Analysis]
Number Citing Articles
1 Myskja BK, Steinsbekk KS. Personalized medicine, digital technology and trust: a Kantian account. Med Health Care Philos 2020;23:577-87. [PMID: 32888101 DOI: 10.1007/s11019-020-09974-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
2 Joshi E, Mighton C, Clausen M, Casalino S, Kim THM, Kowal C, Birken C, Maguire JL, Bombard Y. Primary care provider perspectives on using genomic sequencing in the care of healthy children. Eur J Hum Genet 2020;28:551-7. [PMID: 31804631 DOI: 10.1038/s41431-019-0547-6] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
3 Katz AE, Nussbaum RL, Solomon BD, Rehm HL, Williams MS, Biesecker LG. Management of Secondary Genomic Findings. Am J Hum Genet 2020;107:3-14. [PMID: 32619490 DOI: 10.1016/j.ajhg.2020.05.002] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
4 Greve V, Odom K, Pudner S, Lamb NE, Cooper SJ, East K. Characteristics and experiences of patients from a community-based and consumer-directed hereditary cancer population screening initiative. HGG Adv 2022;3:100055. [PMID: 35047846 DOI: 10.1016/j.xhgg.2021.100055] [Reference Citation Analysis]
5 Vu M, Degeling K, Martyn M, Lynch E, Chong B, Gaff C, IJzerman MJ. Evaluating the resource implications of different service delivery models for offering additional genomic findings. Genet Med 2021;23:606-13. [PMID: 33214711 DOI: 10.1038/s41436-020-01030-8] [Reference Citation Analysis]
6 Christensen KD, Bell M, Zawatsky CLB, Galbraith LN, Green RC, Hutchinson AM, Jamal L, LeBlanc JL, Leonhard JR, Moore M, Mullineaux L, Petry N, Platt DM, Shaaban S, Schultz A, Tucker BD, Van Heukelom J, Wheeler E, Zoltick ES, Hajek C; Imagenetics Metrics Team. Precision Population Medicine in Primary Care: The Sanford Chip Experience. Front Genet 2021;12:626845. [PMID: 33777099 DOI: 10.3389/fgene.2021.626845] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
7 Hagenkord J, Funke B, Qian E, Hegde M, Jacobs KB, Ferber M, Lebo M, Buchanan A, Bick D. Design and Reporting Considerations for Genetic Screening Tests. The Journal of Molecular Diagnostics 2020;22:599-609. [DOI: 10.1016/j.jmoldx.2020.01.014] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
8 Hoell C, Aufox S, Nashawaty N, Myers MF, Smith ME. Comprehension and personal value of negative non-diagnostic genetic panel testing. J Genet Couns 2021;30:418-27. [PMID: 32945059 DOI: 10.1002/jgc4.1327] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Babovic-Vuksanovic D. Genomics as a Scientifically Based Fortune-teller. Mayo Clin Proc 2019;94:7-9. [PMID: 30611456 DOI: 10.1016/j.mayocp.2018.11.008] [Reference Citation Analysis]
10 Kelly MA, Leader JB, Wain KE, Bodian D, Oetjens MT, Ledbetter DH, Martin CL, Strande NT. Leveraging population-based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project. Am J Med Genet C Semin Med Genet 2021;187:83-94. [PMID: 33576083 DOI: 10.1002/ajmg.c.31887] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 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] [Article Influence: 0.5] [Reference Citation Analysis]
12 Powell SN, Byfield G, Bennetone A, Frantz AM, Harrison LK, James-crook ER, Osborne H, Owens TH, Shaw JL, O’daniel J, Milko LV. Parental Guidance Suggested: Engaging Parents as Partners in Research Studies of Genomic Screening for a Pediatric Population. Front Genet 2022;13:867030. [DOI: 10.3389/fgene.2022.867030] [Reference Citation Analysis]
13 Bylstra Y, Lim WK, Kam S, Tham KW, Wu RR, Teo JX, Davila S, Kuan JL, Chan SH, Bertin N, Yang CX, Rozen S, Teh BT, Yeo KK, Cook SA, Jamuar SS, Ginsburg GS, Orlando LA, Tan P. Family history assessment significantly enhances delivery of precision medicine in the genomics era. Genome Med 2021;13:3. [PMID: 33413596 DOI: 10.1186/s13073-020-00819-1] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Ross LF, Clayton EW. Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq. Pediatrics 2019;144:e20191031. [PMID: 31719124 DOI: 10.1542/peds.2019-1031] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 3.3] [Reference Citation Analysis]