Browsing byAuthorTurbitt, E

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Issue DateTitleAuthor(s)
2021-10Uptake 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
2021-09-22Views and experiences of palliative care clinicians in addressing genetics with individuals and families: a qualitative study.White, S; Phillips, J; Turbitt, E; Jacobs, C
2021-09-21Decision making about genetic health information among family dyads: A systematic literature review.Law, WK; Yaremych, HE; Ferrer, R; Richardson, E; Wu, YP; Turbitt, E
2021-07Enrolling Children in Clinical Trials for Genetic Neurodevelopmental Conditions: Ethics, Parental Decisions, and Children's Identities.Turbitt, E; Newson, AJ; Biesecker, BB; Wilfond, BS
2021-06-01Advancing precision public health using human genomics: examples from the field and future research opportunitiesRoberts, MC; Fohner, AE; Landry, L; Olstad, DL; Smit, AK; Turbitt, E; Allen, CG
2021-05-13Dyadic concordance and associations of beliefs with intentions to learn carrier results from genomic sequencingHuelsnitz, CO; Turbitt, E; Taber, JM; Lewis, KL; Biesecker, LG; Biesecker, BB; Klein, WMP
2021-05Engagement and return of results preferences among a primarily African American genomic sequencing research cohort.Lewis, KL; Turbitt, E; Chan, PA; Epps, S; Biesecker, BB; Erby, LAH; Fasaye, G-A; Biesecker, LG
2021-04-19Preferences for and acceptability of receiving pharmacogenomic results by mail: A focus group study with a primarily African-American cohort.Chan, PA; Lewis, KL; Biesecker, BB; Erby, LH; Fasaye, G-A; Epps, S; Biesecker, LG; Turbitt, E
2020-12Parental 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
2020-10-01Molecular phylogenetic analysis of New Zealand mosquito speciesCane, RP; Li, D; Turbitt, E; Chambers, GK
2020-05Perceptions of uncertainties about carrier results identified by exome sequencing in a randomized controlled trial.Umstead, KL; Han, PKJ; Lewis, KL; Miller, IM; Hepler, CL; Thompson, LJ; Wolfsberg, TG; Nguyen, A-D; Fredriksen, MT; Gibney, G; Turbitt, E; Biesecker, LG; Biesecker, BB
2020-05A primer in genomics for social and behavioral investigators.Turbitt, E; Biesecker, BB
2019-10-01Psychosocial, attitudinal, and demographic correlates of cancer-related germline genetic testing in the 2017 Health Information National Trends SurveyRoberts, MC; Turbitt, E; Klein, WMP
2019-08-03Early career investigators and precision public healthAllen, CG; Fohner, AE; Landry, L; Paul, J; Smith, SG; Turbitt, E; Roberts, MC
2019-08-01Ethnic identity and engagement with genome sequencing researchTurbitt, E; Roberts, MC; Hollister, BM; Lewis, KL; Biesecker, LG; Klein, WMP
2019-08-01Fragile X syndrome clinical trials: exploring parental decision-makingD'Amanda, CS; Peay, HL; Wheeler, AC; Turbitt, E; Biesecker, BB
2019-06-01Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview SurveyTurbitt, E; Roberts, MC; Taber, JM; Waters, EA; McNeel, TS; Biesecker, BB; Klein, WMP
2019-05-01Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite studyHart, MR; Biesecker, BB; Blout, CL; Christensen, KD; Amendola, LM; Bergstrom, KL; Biswas, S; Bowling, KM; Brothers, KB; Conlin, LK; Cooper, GM; Dulik, MC; East, KM; Everett, JN; Finnila, CR; Ghazani, AA; Gilmore, MJ; Goddard, KAB; Jarvik, GP; Johnston, JJ; Kauffman, TL; Kelley, WV; Krier, JB; Lewis, KL; McGuire, AL; McMullen, C; Ou, J; Plon, SE; Rehm, HL; Richards, CS; Romasko, EJ; Miren Sagardia, A; Spinner, NB; Thompson, ML; Turbitt, E; Vassy, JL; Wilfond, BS; Veenstra, DL; Berg, JS; Green, RC; Biesecker, LG; Hindorff, LA
2019-05-01Managing the need to tell: Triggers and strategic disclosure of thalassemia major in SingaporeKumar, N; Turbitt, E; Biesecker, BB; Miller, IM; Cham, B; Smith, KC; Rimal, RN
2019-05-01Australians’ views and experience of personal genomic testing: survey findings from the Genioz studySavard, J; Hickerton, C; Tytherleigh, R; Terrill, B; Turbitt, E; Newson, AJ; Wilson, B; Gray, K; Gaff, C; Middleton, A; Stackpoole, E; Metcalfe, SA