Issue Date | Title | Author(s) |
2019-08-01 | Ethnic identity and engagement with genome sequencing research | Turbitt, E; Roberts, MC; Hollister, BM; Lewis, KL; Biesecker, LG; Klein, WMP |
2019-06-01 | Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview Survey | Turbitt, E; Roberts, MC; Taber, JM; Waters, EA; McNeel, TS; Biesecker, BB; Klein, WMP |
2019-08-01 | Fragile X syndrome clinical trials: exploring parental decision-making | D'Amanda, CS; Peay, HL; Wheeler, AC; Turbitt, E; Biesecker, BB |
2019-08-03 | Early career investigators and precision public health | Allen, CG; Fohner, AE; Landry, L; Paul, J; Smith, SG; Turbitt, E; Roberts, MC |
2018-03-01 | Web platform vs in-person genetic counselor for return of carrier results from exome sequencing a randomized clinical trial | Biesecker, BB; Lewis, KL; Umstead, KL; Johnston, JJ; Turbitt, E; Fishler, KP; Patton, JH; Miller, IM; Heidlebaugh, AR; Biesecker, LG |
2019-05-01 | Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study | Metcalfe, SA; Hickerton, C; Savard, J; Stackpoole, E; Tytherleigh, R; Tutty, E; Terrill, B; Turbitt, E; Gray, K; Middleton, A; Wilson, B; Newson, AJ; Gaff, C |
2020-12 | Parental decision making about clinical trial enrollment: A survey of parents of children with Fragile X syndrome. | Turbitt, E; Klein, WMP; Rogers, K; D'Amanda, CS; Biesecker, BB |
2020-05 | A primer in genomics for social and behavioral investigators. | Turbitt, E; Biesecker, BB |
2021-10 | Uptake of Genetic Testing Among Patients with Cancer At Risk for Lynch Syndrome in the National Health Interview Survey. | Actkins, KV; Srinivasan, S; Spees, LP; Turbitt, E; Allen, CG; Roberts, MC |
2022-12 | Do online decision aids reflect new prenatal screening and testing options? An environmental scan and content analysis | Lu, JYT; McKinn, S; Freeman, L; Turbitt, E; Bonner, C |