V. Bonham

“I think if we don’t eat well, we will be sicker”: A Qualitative Perspective on Contributing Factors to Diet Intake and Nutrition Among Adults Living with Sickle Cell Disease in the U.S
20260 citationsauthor #10
Democratizing Education for Sickle Cell Disease Gene Therapy: A Community-Based Model for Creating Patient Education Materials
20250 citationsauthor #1
Enabling discovery of the social determinants of health: using a specialized lens to see beyond the surface
20250 citationsauthor #4
First-in-human gene therapy clinical trials in the media: Exploring patient narratives
20250 citationsauthor #4
The role of religiosity and spirituality in coping with sickle cell disease clinical severity.
20250 citationsauthor #7
Measuring (Mis)trust in the age of COVID-19: viewpoints of vaccine clinical trial participation among individuals living with sickle cell disease
20250 citationsauthor #8
A Holistic Approach to Sickle Cell Disease Severity Using Patient-Reported Outcomes
20240 citationsauthor #6
An Examination of John Henryism in Adults Living with Sickle Cell Disease
20240 citationsauthor #6
Bidirectional Relationship Between Sickle Cell Disease and Food Insecurity: Scoping Review
20243 citationsauthor #6
Leg ulcers are indicators of systemic dysfunction in individuals with sickle cell disease
20241 citationsauthor #4
Advancing genomics to improve health equity
202440 citationsauthor #3
Patient Perceptions on the Advancement of Noninvasive Prenatal Testing for Sickle Cell Disease among Black Women in the United States
20244 citationsauthor #5
Assessing Bias Toward a Black or White Simulated Patient with Obesity in a Virtual Reality-Based Genomics Encounter
20241 citationsauthor #7
"Resilience?" perspectives from adults living with sickle cell disease.
20240 citationsauthor #4
Ancestry-independent risk of venous thromboembolism in individuals with sickle cell trait vs factor V Leiden
20241 citationsauthor #4
Dietary Behaviors and Social Determinants of Health Among Adults Living with Sickle Cell Disease
20230 citationsauthor #13
Views of Adults Living with Sickle Cell Disease on the Theoretical Return of Secondary Genomic Findings.
20231 citationsauthor #5
Race-Based Care and Beliefs Regarding the Etiology of Racial Differences in Health Outcomes.
20232 citationsauthor #6
Equitable delivery of expanded genetic technologies: Considerations for prenatal and reproductive care
20235 citationsauthor #4
Insights on Sickle Cell Disease Therapies in Sierra Leone
20230 citationsauthor #5
Returning Secondary Genomic Findings to a Sickle Cell Disease Cohort
20230 citationsauthor #7
Examining resilience of individuals living with sickle cell disease in the COVID-19 pandemic
20220 citationsauthor #7
Herstory as an Important Force in Bioethics.
20223 citationsauthor #8
Educational considerations based on medical student use of polygenic risk information and apparent race in a simulated consultation.
20222 citationsauthor #7
Examining resilience of individuals living with sickle cell disease in the COVID-19 pandemic
202212 citationsauthor #7
438 “How do you define Resilience?” Examining the Psychological Resilience of Black Adults Living with Sickle Cell Disease (SCD)
20220 citationsauthor #3
Democratizing Knowledge for Sickle Cell Disease Gene Therapy: A Community Based Model for Creating Patient Education Materials
20222 citationsauthor #4
Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?
202228 citationsauthor #7
Navigating Access to Cancer Care: Identifying Barriers to Precision Cancer Medicine.
202210 citationsauthor #5
Examining Sickle Cell Trait Associated Clinical Outcomes in the All of Us research Program
20222 citationsauthor #5
Association of Sickle Cell Trait and Venous Thromboembolism in the 23andMe Cohort
20221 citationsauthor #4
Splenic infarction in sickle cell trait: A comprehensive systematic review of case studies
202115 citationsauthor #6
Treatment decision-making in sickle cell disease patients
20218 citationsauthor #2
The genomics workforce must become more diverse: a strategic imperative.
202135 citationsauthor #1
Lower hair cortisol among patients with sickle cell disease may indicate decreased adrenal reserves.
20212 citationsauthor #10
Cultivating diversity as an ethos with an anti-racism approach in the scientific enterprise
202123 citationsauthor #10
Insights into the skin microbiome of sickle cell disease leg ulcers
202113 citationsauthor #10
Social support networks of adults with sickle cell disease
202114 citationsauthor #3
Ethical Issues in Genetics and Infectious Diseases Research: An Interdisciplinary Expert Review.
20213 citationsauthor #2
Practices and Attitudes toward Returning Genomic Research Results to Low-Resource Research Participants
20218 citationsauthor #4
Evolving use of ancestry, ethnicity, and race in genetics research—A survey spanning seven decades
202140 citationsauthor #7
Pragmatic Clinical Trial-Collateral Findings: Recognizing the Needs of Low-Resource Research Participants
20204 citationsauthor #5
The Meaning of Informed Consent: Genome Editing Clinical Trials for Sickle Cell Disease
202015 citationsauthor #6
Strategic vision for improving human health at The Forefront of Genomics
2020265 citationsauthor #27
Alaska Native genomic research: perspectives from Alaska Native leaders, federal staff, and biomedical researchers
202022 citationsauthor #6
Immunophenotypes and Clinical Outcomes in Adult Patients with Sickle Cell Disease: Lymphopenia Correlates with End Organ Damage
20200 citationsauthor #8
Emergency Department Utilization for Patients Living With Sickle Cell Disease: Psychosocial Predictors of Health Care Behaviors
202019 citationsauthor #8
Perspectives of Sickle Cell Disease Stakeholders on Heritable Genome Editing
201917 citationsauthor #11
Clinical Implications of Active Coping on Sleep: John Henryism in a Sickle Cell Disease Cohort
20193 citationsauthor #1
Defining and Achieving Health Equity in Genomic Medicine.
201964 citationsauthor #4
Social and behavioral science at the forefront of genomics: Discovery, translation, and health equity.
20198 citationsauthor #4
Intersectionality and Clinical Decision Making: The Role of Race
20197 citationsauthor #3
Somatic Genome Editing in Sickle Cell Disease: Rewriting a More Just Future
20196 citationsauthor #1
How Can Law Support Development of Genomics and Precision Medicine to Advance Health Equity and Reduce Disparities?
20196 citationsauthor #2
Blending Insights from Implementation Science and the Social Sciences to Mitigate Inequities in Screening for Hereditary Cancer Syndromes
201912 citationsauthor #4
Correction to: Physician Knowledge of Human Genetic Variation, Beliefs About Race and Genetics, and Use of Race in Clinical Decision-making
20190 citationsauthor #3
The clinical application of gene editing: ethical and social issues.
201935 citationsauthor #3
Hair Cortisol Is a Potential Indicator of Adrenal Insufficiency in Individuals with Sickle Cell Disease
20190 citationsauthor #10
Advocacy and actions to address disparities in access to genomic health care: A report on a National Academies workshop.
20199 citationsauthor #2
A Comparison of Physicians' and Nurse Practitioners' Use of Race in Clinical Decision-Making.
20195 citationsauthor #6
Race and Ethnicity Data in Research-Reply.
20192 citationsauthor #1
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.
201943 citationsauthor #7
Should Electronic Health Record-Derived Social and Behavioral Data Be Used in Precision Medicine Research?
201826 citationsauthor #2
The Role of the Health Care Provider in Building Trust Between Patients and Precision Medicine Research Programs
201826 citationsauthor #2
Nutritional supplement profile of adults with sickle cell disease
20184 citationsauthor #2
Engagement and Education of the Sickle Cell Disease Community: What Sickle Cell Disease Patients and Parents Want to Know about CRISPR Genome Editing
20181 citationsauthor #4
Moving towards a cure in genetics: what is needed to bring somatic gene therapy to the clinic?
201813 citationsauthor #4
Clinical Outcomes Associated With Sickle Cell Trait
201857 citationsauthor #11
A CRISPR focus on attitudes and beliefs toward somatic genome editing from stakeholders within the sickle cell disease community
201839 citationsauthor #4
Examining How Race, Ethnicity, and Ancestry Data Are Used in Biomedical Research.
2018131 citationsauthor #1
Negotiating Deliberative Ideals in Theory and Practice : A Case Study in " Hybrid Design "
20181 citationsauthor #6
Physician Knowledge of Human Genetic Variation, Beliefs About Race and Genetics, and Use of Race in Clinical Decision-making
201812 citationsauthor #3
Coagulation Profile of Sickle Cell Patients with Leg Ulcers
20180 citationsauthor #9
The Clinical Imperative for Inclusivity: Race, Ethnicity, and Ancestry (REA) in Genomics
2018122 citationsauthor #14
Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice.
2018259 citationsauthor #5
Enhancing diversity to reduce health information disparities and build an evidence base for genomic medicine.
201843 citationsauthor #2
Prioritizing diversity in human genomics research
2017324 citationsauthor #2
Genomics for all in the 21st century?
201715 citationsauthor #2
The Psychosocial Impact of Leg Ulcers in Sickle Cell Disease
20170 citationsauthor #1
Leveraging the learning health care model to improve equity in the age of genomic medicine
201719 citationsauthor #2
Primary Care Physicians' Collection, Comfort, and Use of Race and Ethnicity in Clinical Practice in the United States
201725 citationsauthor #1
The psychosocial impact of leg ulcers in patients with sickle cell disease: I don’t want them to know my little secret
201736 citationsauthor #6
Nurses' Use of Race in Clinical Decision Making.
20169 citationsauthor #6
Health Disparities and the Microbiome.
201672 citationsauthor #4
Will Precision Medicine Move Us beyond Race?
201695 citationsauthor #1
Towards a more representative morphology: clinical and ethical considerations for including diverse populations in diagnostic genetic atlases
201632 citationsauthor #2
Taking a Stand: The Genetics Community's Responsibility for Intelligence Research.
201510 citationsauthor #2
Physicians’ Anxiety Due to Uncertainty and Use of Race in Medical Decision Making
201427 citationsauthor #2
Physicians’ knowledge, beliefs, and use of race and human genetic variation: new measures and insights
201431 citationsauthor #1
Multi-ethnic minority nurses' knowledge and practice of genetics and genomics.
201442 citationsauthor #8
National nursing workforce survey of nursing attitudes, knowledge and practice in genomics.
201371 citationsauthor #4
What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report
2013126 citationsauthor #7
Framing the research agenda for sickle cell trait: Building on the current understanding of clinical events and their potential implications
2012105 citationsauthor #2
Where Do Men Get Information about Benign Prostatic Hyperlasia (Bph): Is There a Difference between College Educated and Non-College Educated Older Men?
20110 citationsauthor #2
Goal-striving stress and the mental health of college-educated Black American men: the protective effects of system-blame.
201138 citationsauthor #3
Abstract ED04-02: Are we moving beyond race in clinical care? Lessons from the RACE Project
20110 citationsauthor #1
Effects of Incentives and Prenotification on Response Rates and Costs in a National Web Survey of Physicians
201168 citationsauthor #5
Is race medically relevant? A qualitative study of physicians' attitudes about the role of race in treatment decision-making
201154 citationsauthor #6
Inclusion of Racial and Ethnic Minorities in Genetic Research: Advance the Spirit by Changing the Rules?
201136 citationsauthor #3
Contents Vol. 13, 2010
20100 citationsauthor #6

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