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Shawneequa Callier
Shawneequa Callier
Associate Professor
Zweryfikowany adres z email.gwu.edu
Tytuł
Cytowane przez
Cytowane przez
Rok
Diversity and inclusion in genomic research: why the uneven progress?
AR Bentley, S Callier, CN Rotimi
Journal of community genetics 8 (4), 255-266, 2017
3082017
Evaluating the promise of inclusion of African ancestry populations in genomics
AR Bentley, SL Callier, CN Rotimi
NPJ genomic medicine 5 (1), 5, 2020
1292020
Will precision medicine move us beyond race?
VL Bonham, SL Callier, CD Royal
The New England journal of medicine 374 (21), 2003, 2016
1152016
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
552016
Swabbing students: should universities be allowed to facilitate educational DNA testing?
SL Callier
The American Journal of Bioethics 12 (4), 32-40, 2012
472012
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
442023
Taking a stand: The genetics community's responsibility for intelligence research
SL Callier, VL Bonham
Hastings Center Report 45 (S1), S54-S58, 2015
412015
Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects
KJ Karczewski, R Gupta, M Kanai, W Lu, K Tsuo, Y Wang, RK Walters, ...
MedRxiv, 2024.03. 13.24303864, 2024
372024
Why personalized medicine will fail if we stay the course
E Ramos, SL Callier, CN Rotimi
Personalized medicine 9 (8), 839-847, 2012
362012
The use of racial categories in precision medicine research
SL Callier
Ethnicity & disease 29 (Suppl 3), 651, 2019
342019
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
342012
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
272021
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
252019
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
242021
Exclusion cycles: Reinforcing disparities in medicine
A Bracic, SL Callier, WN Price
Science 377 (6611), 1158-1160, 2022
232022
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
222018
Racial equity, diversity and inclusion in bioethics: Recommendations from the Association of Bioethics Program Directors Presidential Task Force
SSJ Lee, A Walker, SL Callier, FE Fletcher, C Galarneau, N Garrison, ...
The American Journal of Bioethics 24 (10), 3-14, 2024
202024
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
162019
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
162016
Genomic data-sharing: what will be our legacy?
S Callier, R Husain, R Simpson
Frontiers in genetics 5, 34, 2014
162014
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