| Issue Date | Title | Author(s) |
| 2019-05-01 | Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study | Hart, 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 |
| 2018-08-01 | Australians’ views on personal genomic testing: focus group findings from the Genioz study | Metcalfe, SA; Hickerton, C; Savard, J; Terrill, B; Turbitt, E; Gaff, C; Gray, K; Middleton, A; Wilson, B; Newson, AJ |
| 2018-09-06 | Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot | Sapp, JC; Johnston, JJ; Driscoll, K; Heidlebaugh, AR; Miren Sagardia, A; Dogbe, DN; Umstead, KL; Turbitt, E; Alevizos, I; Baron, J; Bönnemann, C; Brooks, B; Donkervoort, S; Jee, YH; Linehan, WM; McMahon, FJ; Moss, J; Mullikin, JC; Nielsen, D; Pelayo, E; Remaley, AT; Siegel, R; Su, H; Zarate, C; Barnabas, BB; Bouffard, GG; Brooks, SY; Coleman, H; Dekhtyar, L; Guan, X; Han, J; Ho, SL; Legaspi, R; Maduro, QL; Masiello, CA; McDowell, JC; Montemayor, C; Park, M; Riebow, NL; Schandler, K; Scharer, C; Schmidt, B; Sison, C; Stantripop, S; Thomas, JW; Thomas, PJ; Vemulapalli, M; Young, AC; Manolio, TA; Biesecker, BB; Biesecker, LG |
| 2018-02-01 | Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention | Haakonsen Smith, C; Turbitt, E; Muschelli, J; Leonard, L; Lewis, KL; Freedman, B; Muratori, M; Biesecker, BB |
| 2019-08-01 | Ethnic identity and engagement with genome sequencing research | Turbitt, E; Roberts, MC; Hollister, BM; Lewis, KL; Biesecker, LG; Klein, WMP |
| 2019-04-01 | Communication about genetic testing with breast and ovarian cancer patients: a scoping review | Jacobs, C; Patch, C; Michie, S |
| 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 |
| 2019-10 | Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell? | Taylor, S; Rodrigues, M; Poke, G; Wake, S; McEwen, A |
| 2020-07 | Mainstreaming genetics and genomics: a systematic review of the barriers and facilitators for nurses and physicians in secondary and tertiary care. | White, S; Jacobs, C; Phillips, J |
| 2020-02 | Who should access germline genome sequencing? A mixed methods study of patient views. | Best, MC; Butow, P; Jacobs, C; Savard, J; Biesecker, B; Ballinger, ML; Bartley, N; Davies, G; Napier, CE; Smit, AK; Thomas, DM; Newson, AJ; Members of the PiGeOn Project |
