Biblio

Found 12 results
Filters: Keyword is Genomics  [Clear All Filters]
2024
James JElyse, Riddle L, Koenig B, Joseph G. Moving toward Equity through Embedded ELSI Ethnography. Hastings Cent Rep. 2024 ;54 Suppl 2:S93-S101.
2022
Jeske M, Vasquez E, Fullerton SM, Saperstein A, Bentz M, Foti N, Shim JK, Lee SSoo-Jin. Beyond inclusion: Enacting team equity in precision medicine research. PLoS One. 2022 ;17(2):e0263750.
Norstad M, Outram S, Brown JEH, Zamora AN, Koenig BA, Risch N, Norton ME, Slavotinek A, Ackerman SL. The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research. Genet Med. 2022 ;24(2):410-418.
Wang T, Antonacci-Fulton L, Howe K, Lawson HA, Lucas JK, Phillippy AM, Popejoy AB, Asri M, Carson C, Chaisson MJP, et al. The Human Pangenome Project: a global resource to map genomic diversity. Nature. 2022 ;604(7906):437-446.
Smith HStevens, Morain SR, Robinson JOliver, Canfield I, Malek J, Rubanovich CKseniya, Bloss CS, Ackerman SL, Biesecker B, Brothers KB, et al. Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development. Patient. 2022 ;15(3):317-328.
Rego S, Hoban H, Outram S, Zamora AN, Chen F, Sahin-Hodoglugil N, Anguiano B, Norstad M, Yip T, Lianoglou B, et al. Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach. Genet Med. 2022 ;24(6):1206-1216.
Ghazal LV, Cole S, Salsman JM, Wagner L, Duan F, Gareen I, Lux L, Parsons SK, Cheung C, Loeb DM, et al. Social Genomics as a Framework for Understanding Health Disparities Among Adolescent and Young Adult Cancer Survivors: A Commentary. JCO Precis Oncol. 2022 ;6:e2100462.
Johansson A, Dar H, Veer LJ van 't, Tobin NP, Perez-Tenorio G, Nordenskjöld A, Johansson U, Hartman J, Skoog L, Yau C, et al. Twenty-Year Benefit From Adjuvant Goserelin and Tamoxifen in Premenopausal Patients With Breast Cancer in a Controlled Randomized Clinical Trial. J Clin Oncol. 2022 ;40(35):4071-4082.
2021
McInnes G, Sharo AG, Koleske ML, Brown JEH, Norstad M, Adhikari AN, Wang S, Brenner SE, Halpern J, Koenig BA, et al. Opportunities and challenges for the computational interpretation of rare variation in clinically important genes. Am J Hum Genet. 2021 ;108(4):535-548.
2020
Popejoy AB, Crooks KR, Fullerton SM, Hindorff LA, Hooker GW, Koenig BA, Pino N, Ramos EM, Ritter DI, Wand H, et al. Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures. Am J Hum Genet. 2020 ;107(1):72-82.
Bliss C. Conceptualizing Race in the Genomic Age. Hastings Cent Rep. 2020 ;50 Suppl 1:S15-S22.
Flowers E, Leutwyler H, Shim JK. Direct-to-consumer genomic testing: Are nurses prepared?. Nursing. 2020 ;50(8):48-52.