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3. Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing. Himes P; Kauffman TL; Muessig KR; Amendola LM; Berg JS; Dorschner MO; Gilmore M; Nickerson DA; Reiss JA; Richards CS; Rope AF; Simpson DK; Wilfond BS; Jarvik GP; Goddard KAB Genet Med; 2017 Jul; 19(7):803-808. PubMed ID: 28079899 [TBL] [Abstract][Full Text] [Related]
4. Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results. Werner-Lin A; Zaspel L; Carlson M; Mueller R; Walser SA; Desai R; Bernhardt BA Am J Med Genet A; 2018 Mar; 176(3):578-588. PubMed ID: 29446570 [TBL] [Abstract][Full Text] [Related]
5. Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies. Robinson JO; Wynn J; Biesecker B; Biesecker LG; Bernhardt B; Brothers KB; Chung WK; Christensen KD; Green RC; McGuire AL; Hart MR; Griesemer I; Patrick DL; Rini C; Veenstra D; Cronin AM; Gray SW Genet Med; 2019 Dec; 21(12):2781-2790. PubMed ID: 31189963 [TBL] [Abstract][Full Text] [Related]
6. 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 Genet Med; 2019 May; 21(5):1100-1110. PubMed ID: 30287922 [TBL] [Abstract][Full Text] [Related]
8. Clinical providers' experiences with returning results from genomic sequencing: an interview study. Wynn J; Lewis K; Amendola LM; Bernhardt BA; Biswas S; Joshi M; McMullen C; Scollon S BMC Med Genomics; 2018 May; 11(1):45. PubMed ID: 29739461 [TBL] [Abstract][Full Text] [Related]
9. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing. Jamal L; Robinson JO; Christensen KD; Blumenthal-Barby J; Slashinski MJ; Perry DL; Vassy JL; Wycliff J; Green RC; McGuire AL AJOB Empir Bioeth; 2017; 8(2):82-88. PubMed ID: 28949844 [TBL] [Abstract][Full Text] [Related]
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11. Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium. Suckiel SA; O'Daniel JM; Donohue KE; Gallagher KM; Gilmore MJ; Hendon LG; Joseph G; Lianoglou BR; Mathews JM; Norton ME; Odgis JA; Poss AF; Rego S; Scollon S; Yip T; Amendola LM J Pers Med; 2021 Mar; 11(3):. PubMed ID: 33805616 [TBL] [Abstract][Full Text] [Related]
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14. Disclosure of genetic research results to members of a founder population. Anderson RL; Murray K; Chong JX; Ouwenga R; Antillon M; Chen P; Diaz de Leon L; Swoboda KJ; Lester LA; Das S; Ober C; Waggoner DJ J Genet Couns; 2014 Dec; 23(6):984-91. PubMed ID: 24777552 [TBL] [Abstract][Full Text] [Related]
15. Counseling for personal health implications identified during reproductive genetic carrier screening. Gbur S; Mauney L; Gray KJ; Wilkins-Haug L; Guseh S Prenat Diagn; 2021 Oct; 41(11):1460-1466. PubMed ID: 34426984 [TBL] [Abstract][Full Text] [Related]
16. Generating a taxonomy for genetic conditions relevant to reproductive planning. Korngiebel DM; McMullen CK; Amendola LM; Berg JS; Davis JV; Gilmore MJ; Harding CO; Himes P; Jarvik GP; Kauffman TL; Kennedy KA; Simpson DK; Leo MC; Lynch FL; Quigley DI; Reiss JA; Richards CS; Rope AF; Schneider JL; Goddard KA; Wilfond BS Am J Med Genet A; 2016 Mar; 170(3):565-73. PubMed ID: 26889673 [TBL] [Abstract][Full Text] [Related]
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19. Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium. Amendola LM; Robinson JO; Hart R; Biswas S; Lee K; Bernhardt BA; East K; Gilmore MJ; Kauffman TL; Lewis KL; Roche M; Scollon S; Wynn J; Blout C J Genet Couns; 2018 Sep; 27(5):1220-1227. PubMed ID: 29497922 [TBL] [Abstract][Full Text] [Related]
20. Patient perspectives on the use of categories of conditions for decision making about genomic carrier screening results. Kraft SA; McMullen CK; Porter KM; Kauffman TL; Davis JV; Schneider JL; Goddard KAB; Wilfond BS Am J Med Genet A; 2018 Feb; 176(2):376-385. PubMed ID: 29250907 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]