| Diversity and inclusion in genomic research: why the uneven progress? AR Bentley, S Callier, CN Rotimi Journal of community genetics 8, 255-266, 2017 | 257 | 2017 |
| Will precision medicine move us beyond race? VL Bonham, SL Callier, CD Royal The New England journal of medicine 374 (21), 2003, 2016 | 111 | 2016 |
| Evaluating the promise of inclusion of African ancestry populations in genomics AR Bentley, SL Callier, CN Rotimi NPJ genomic medicine 5 (1), 5, 2020 | 107 | 2020 |
| Ethical, legal, and social implications of personalized genomic medicine research: current literature and suggestions for the future SL Callier, R Abudu, MJ Mehlman, ME Singer, D Neuhauser, ... Bioethics 30 (9), 698-705, 2016 | 52 | 2016 |
| Swabbing students: should universities be allowed to facilitate educational DNA testing? SL Callier The American Journal of Bioethics 12 (4), 32-40, 2012 | 46 | 2012 |
| Taking a stand: The genetics community's responsibility for intelligence research SL Callier, VL Bonham Hastings Center Report 45 (S1), S54-S58, 2015 | 41 | 2015 |
| Why personalized medicine will fail if we stay the course E Ramos, SL Callier, CN Rotimi Personalized medicine 9 (8), 839-847, 2012 | 37 | 2012 |
| How anonymous is ‘anonymous’? Some suggestions towards a coherent universal coding system for genetic samples H Schmidt, S Callier Journal of Medical Ethics 38 (5), 304-309, 2012 | 34 | 2012 |
| The use of racial categories in precision medicine research SL Callier Ethnicity & disease 29 (Suppl 3), 651, 2019 | 30 | 2019 |
| The emergence of genomic research in Africa and new frameworks for equity in biomedical research AR Bentley, S Callier, C Rotimi Ethnicity & disease 29 (Suppl 1), 179, 2019 | 24 | 2019 |
| Multi-Ancestry Meta-Analysis yields novel genetic discoveries and ancestry-specific associations P Turley, AR Martin, G Goldman, H Li, M Kanai, RK Walters, JB Jala, K Lin, ... BioRxiv, 2021.04. 23.441003, 2021 | 22 | 2021 |
| Wrestling with social and behavioral genomics: risks, potential benefits, and ethical responsibility MN Meyer, PS Appelbaum, DJ Benjamin, SL Callier, N Comfort, D Conley, ... Hastings Center Report 53, S2-S49, 2023 | 20 | 2023 |
| Complicated legacies: The human genome at 20 KM Jones, R Cook-Deegan, CN Rotimi, SL Callier, AR Bentley, H Stevens, ... Science 371 (6529), 564-569, 2021 | 20 | 2021 |
| Trust, precision medicine research, and equitable participation of underserved populations M Sabatello, S Callier, NA Garrison, EG Cohn The American Journal of Bioethics 18 (4), 34-36, 2018 | 20 | 2018 |
| Genomic data-sharing: what will be our legacy? S Callier, R Husain, R Simpson Frontiers in genetics 5, 63295, 2014 | 16 | 2014 |
| Impact of a personal CYP2D6 testing workshop on physician assistant student attitudes toward pharmacogenetics TJ O'Brien, S LeLacheur, C Ward, NH Lee, S Callier, AF Harralson Pharmacogenomics 17 (4), 341-352, 2016 | 15 | 2016 |
| Exclusion cycles: Reinforcing disparities in medicine A Bracic, SL Callier, WN Price Science 377 (6611), 1158-1160, 2022 | 14 | 2022 |
| Cardiologists' perspectives on race-based drug labels and prescribing within the context of treating heart failure SL Callier, BA Cunningham, J Powell, MA McDonald, CDM Royal Health equity 3 (1), 246-253, 2019 | 12 | 2019 |
| Diversity and inclusion in unregulated mHealth research: addressing the risks S Callier, SM Fullerton The Journal of Law, Medicine & Ethics 48 (1_suppl), 115-121, 2020 | 11 | 2020 |
| Genetic diseases and the duty to disclose S Callier, R Simpson AMA Journal of Ethics 14 (8), 640-644, 2012 | 11 | 2012 |
Nanibaa' GarrisonUniversity of California Los AngelesEmail confirmado em socgen.ucla.edu
