Amy McGuire Lab

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About the Lab

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Amy McGuire, J.D., Ph.D., is the Leon Jaworski Professor of Biomedical Ethics and Director of the Center for Medical Ethics and Health Policy at 7m��Ƶ. She researches ethical and policy issues related to emerging technologies and innovative therapeutics, with a particular focus on genetics and genomics, neuropsychology, and the clinical integration of novel neurological devices and psychedelics. She receives research funding from the National Institutes of Health and is the founding director of the Ethical Legal Implication of PSychedelics in Society (ELIPSIS) program.

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Collaborators

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Current Projects

As wastewater research and monitoring programs develop and evolve beyond SARS-CoV-2 to a wide range of possible pathogens (viruses, bacteria, and protozoa), one critical challenge is determining what information ought to be shared, with whom, and how.

Wastewater research and monitoring can provide early warning of the spread of known diseases of public health importance and inform public health responses, but it can also provide highly sensitive and potentially stigmatizing information, raising ethical, legal, and social implication (ELSI) considerations, including how to communicate information in a way that maximizes benefits and builds public trust while protecting privacy and avoiding the exacerbation of health inequities. EMPOWER is an innovative embedded ELSI research project that will directly impact the development and implementation of strategies for communicating information from a statewide wastewater research and monitoring program in Texas. This project will collect critical empirical data from stakeholders and engage diverse members of the community to identify and develop strategies to address the ELSI considerations of communicating information from public health research.

The objective of EMPOWER is to develop a strategy for responsible reporting of information from wastewater monitoring in the state of Texas that is feasible and reflects community members’ values and perspectives. We will collaborate with the Texas Epidemic Public Health Institute (TEPHI) Wastewater Consortium (TWC) and its Action Plan Working Group to achieve the following specific aims:

In Aim 1, we will identify facilitators and barriers to results disclosure by conducting embedded ELSI research (participant observation) and interviews with the TEPHI Action Plan Working Group members and other stakeholders involved in the TWC.
In Aim 2, we will assess community members’ perspectives about results disclosures by conducting community engagement studios across Texas and a statewide survey.
In Aim 3, we will generate evidence-based recommendations for results disclosure and develop a communication platform for community members’ review and feedback.

Our overarching goal is to develop ethical guidelines for the dissemination of results from wastewater research and monitoring programs.

Supported by: R01ES036232, Grant funding from National Institutes of Health, National Institute of Environmental Health Science, Office of the Director, National Human Genome Research Institute

Project Personnel

Amy McGuire – mPI

Jennifer Deegan – mPI, UTHealth Houston

Faith Fletcher – Co-I

Christi Guerrini – Co-I

Mary Majumder – Co-I

Rosalia Guerrero – Community health worker, UTHealth Houston

Norah Crossnohere – Consultant, patient-centered outcomes researcher, Ohio State University

Shannon-Claire Barnes, Clinical research associate

Jill Robinson – Research manager

Eric Boerwinkle – Advisory committee chair, UTHealth Houston

Anthony Maresso – Advisory committee member

Cheryl Walker – Advisory committee member

After nearly a 50-year hiatus, there has been a resurgence of research on the use of psychedelics to treat a wide range of neuropsychiatric conditions. The FDA designated MDMA and psilocybin breakthrough therapies for PTSD and severe depression, respectively and is anticipated to approve the first psychedelic drug within the next two years. The therapeutic potential of psychedelics has been widely publicized, and patients are now inquiring about the availability and advisability of psychedelic use. Meanwhile, several US cities and both Oregon and Colorado have decriminalized or deprioritized enforcement for at least some psychedelics, with many others considering similar legislation. This growing public enthusiasm, combined with bipartisan advocacy for regulatory reform, has led to an increase in the number of companies offering private or group psychedelic retreats, often without the involvement of licensed healthcare professionals. Yet little is known about how these retreats are run, and because they typically take place in other countries, there is no oversight of their practices. Ethical concerns are mounting regarding potential for off-label and unregulated use of psychedelics without a corresponding evidence-base, leap-frogging established and safe interventions, and commercial abuse. Unchecked, such issues pose clear risk for the responsible and safe uptake of psychedelic therapies that could affect consumer safety, have legal implications, and deleteriously impact patient trust in psychiatric practice. Despite these concerns, no studies to date have systematically examined the use of psychedelics in these unregulated settings or the ethical, legal, and social implications of such use.

The overall goal of this research is to examine the appropriate role (scope, value, and legitimacy) of healthcare gatekeeping for ensuring safe and responsible use of psychedelics.

Specific aims of this project include:

Assess the current state of unregulated psychedelic retreats that are advertised in the U.S.
Examine the ethical, legal, and social implications of these programs from the perspective of those participating in them.
Provide recommendations for the appropriate role (scope, value, and legitimacy) of healthcare gatekeeping in the context of unregulated psychedelic retreats, informed by the results of the first two aims.

Funded by: The Ortus Foundation

Media

The has been ongoing since 2013. The Initiative “is aimed at revolutionizing our understanding of the human brain” through the “development and application of innovative technologies” to deepen our understandings of how the brain and neural circuits interact in health and disease (The BRAIN Initiative, NIH, 2021).

Data sharing is essential to promote equity and maximize the impact of the significant public investment in the BRAIN Initiative. Data sharing plans are now required for BRAIN funding, but there is an urgent need to develop specific policies and practices that are empirically informed and address ethical challenges and concerns related to sharing human data from BRAIN research. Our own experience and research with investigators conducting BRAIN Initiative studies of closed loop or adaptive deep brain stimulation, for instance, suggests that the practice of sharing data is inconsistent and incomplete, despite broad agreement that it is important. Some ethical challenges relate to privacy, consent, the interoperability of data types and sharing platforms, and competing commercial and processional interests.

The specific objectives of BRAINshare: Sharing Data in BRAIN Initiative Studies are to engage key stakeholders in a deliberative process to identify challenges and concerns specific to sharing human data from the BRAIN Initiative and to generate empirically informed policy and practice options to facilitate responsible sharing of this data.

In Aim 1, we will use informational interviews and document analysis to identify BRAIN Initiative-specific data-sharing challenges, as well as relevant policy and practice considerations.
In Aim 2, we will use semi-structured interviews and surveys to evaluate BRAIN Initiative research participants’ attitudes, preferences, and concerns about data sharing and brain privacy.
In Aim 3, we will employ a modified policy Delphi process with diverse stakeholders to prioritize challenges and generate and evaluate policy and practice options that address high-priority challenges.

The long-term goals of this research program are to develop, test, and disseminate strategies to improve data sharing in biomedical research associated with human neuroscience. The overall objective of this project is to apply our combined expertise in neuroscience, neuroethics, social science, law, and science policy to identify challenges and concerns and generate empirically informed policy and practice options that facilitate responsible data sharing within the NIH BRAIN Initiative.

Supported by: R01MH126937, Grant funding from BRAIN Initiative - National Institute of Mental Health of the National Institutes of Health

Presentations

Sharing Data: Speedbumps on the Translation Trail. ELSIcon2022: Innovating for a Just and Equitable Future. Cook-Deegan R, Maxson Jones K, Rahimzadeh V, Spector-Bagdady K (2022).

The Montreal Neurological Institute: A case study in “open” neuroscience. The BRAIN Initiative Meeting. Skvarkova Z, Maxson Jones K, Robinson J, McGuire A, Sheth S, Cook-Deegan R (2022).

Paving the Way to a More Interconnected Community of BRAINs. The BRAIN Initiative Meeting. Iyer S, Maxson Jones K, Robinson J, Cook-Deegan R, Guerrini C, Lázaro-Muñoz G, Majumder M, Sheth S, McGuire A (2022).

BRAINshare: Sharing Data in BRAIN Initiative Studies. The BRAIN Initiative Meeting. Maxson Jones K, Robinson J, Cook-Deegan R, Guerrini C, Lázaro-Muñoz G, Majumder M, Sheth S, McGuire A (2022).

Data Sharing Challenges in Academic-Industry Collaborations in the BRAIN Initiative. The BRAIN Initiative Meeting. Noor I, Maxson Jones K, Robinson J, Cook-Deegan R, Guerrini C, Lázaro-Muñoz G, Majumder M, Sheth S, McGuire A (2022).

Publications

Rahimzadeh V, Jones KM, Majumder MA, et al. Benefits of sharing neurophysiology data from the BRAIN Initiative Research Opportunities in Humans Consortium [published online ahead of print, 2023 Nov 3]. Neuron. 2023;S0896-6273(23)00717-1. doi:10.1016/j.neuron.2023.09.029

Supplement: A Case Study on Autism in Data Sharing Practices

Project Description

This one-year supplement project aims to conduct a case study on ethical data sharing challenges in autism research and how to address data sharing practices that lack diversity, equity, and inclusion considerations. Data will be collected through a literature review and in-depth interviews with diverse stakeholders to explore challenges and potential solutions to address such ethical and policy challenges in data sharing. This case study will serve as an additional research input that informs the ongoing Delphi process in the BRAINshare Project’s Aim 3 and shapes the Project’s broader policy recommendations.

Supported by: R01MH126937-03S1, National Institute of Mental Health, NIH, Research Supplement to Promote Diversity in Health-Related Research Program

Project team: Zuzana Skvarkova (Arizona State University), Robert Cook-Deegan (Arizona State University, co-mentor) and Amy McGuire (co-mentor)

After the Golden State Killer: Public Preferences and Policy Implications of Police Use of Genetic Data

In 2018, the arrest of the alleged Golden State Killer made headlines around the world. He was identified using a controversial new technique called investigative genetic genealogy (IGG). This technique involves uploading crime scene DNA to genetic genealogy databases with the intention of identifying a criminal offender’s genetic relatives and, eventually, locating the offender in their family tree. Since 2018, according to one expert, IGG has helped lead to the successful identification of over 1,000 violent criminal suspects.

At the same time, the technique has been challenged by those who argue it violates fundamental privacy interests of database participants and their families. Some believe that these privacy concerns are so compelling that IGG threatens to undermine public participation in clinical and research genetic databases, especially those maintained by the government.

Past studies—including our own—have demonstrated that individuals are concerned about genetic privacy, yet they are willing to share their genetic data with certain individuals, for particular reasons, and under specific conditions. But all of these studies pre-date IGG and none probed participation by law enforcement in genetic genealogy or other recreational genetic databases. Understanding the complex trade-offs that the public makes when assessing the value and acceptability of law enforcement use of genetic data will be important in ensuring that IGG-relevant policies and practices that are adopted strike a balance between safety and privacy that is acceptable to the public.

This project involves:

Qualitative interviews to characterize and forecast law enforcement participation in genetic genealogy databases.
Focus groups and a discrete choice experiment to measure preferences related to law enforcement participation in genetic genealogy databases.
A modified policy Delphi to develop best practices related to law enforcement participation in genetic genealogy databases.

Additional project materials available at: .

Supported by: R01HG011268, National Human Genome Research Institute, NIH, 2020-2024

FORENSEQ is a trademark of Verogen, Inc. and Qiagen, N.V. The ForenSeq Study is not affiliated with the FORENSEQ mark.

Publications

Dahlquist, J, Robinson, JO, Daoud, A, Bash-Brooks, W, McGuire, AL, Guerrini, CJ, Fullerton, SM. Public perspectives on investigative genetic genealogy: Findings from a national focus group study. AJOB Empir Bioeth. 2024 1–11.
Guerrini CJ, Wickenheiser RA, Bettinger B, McGuire AL, Fullerton SM. Four misconceptions about investigative genetic genealogy. J Law Biosci. 2021;8(1):lsab001. Published 2021 Apr 13. doi:10.1093/jlb/lsab001
Guerrini CJ, Robinson JO, Petersen D, McGuire AL. Should police have access to genetic genealogy databases? Capturing the Golden State Killer and other criminals using a controversial new forensic technique. PLoS Biol. 2018;16(10):e2006906. Published 2018 Oct 2. doi:10.1371/journal.pbio.2006906
Ram N, Guerrini CJ, McGuire AL. Genealogy databases and the future of criminal investigation. Science. 2018;360(6393):1078-1079. doi:10.1126/science.aau1083
Guerrini CJ, Bash Brooks W, Robinson JO, Fullerton SM, Zoorob E, McGuire AL. IGG in the trenches: results of an in-depth interview study on the practice, politics, and future of investigative genetic genealogy. Forensic Science International; 2024;356. Published 2024 Mar.
Campmoamor NB, Guerrini CJ, Bash Brooks W, Bridges JFP, Crossnohere NL. Pretesting discrete‑choice experiments: A guide for researchers. Patient.2024;17,109-120. Published 16 Feb 2024.
McGuire AL, Wickenheiser R, Budowle B, Gurney D, Guerrini CJ. Solving crimes while protecting genetic privacy. Forensic Gen; Published 2023 Dec 7.
Guerrini CJ, Gurney D, Kramer S, Moore, C, Press M, McGuire AL. State genetic privacy statutes: Good intentions, unintended consequences? Bill of Health; Published 2023 Aug 10.
Guerrini CJ, McGuire, AL. Studying public preferences and policy options for investigative genetic genealogy. ISHI News. Publishes 2021 Nov 09
Guerrini CJ, Wickenheiser RA, Bettinger B, McGuire AL, Fullerton SM. Four misconceptions about investigative genetic genealogy. J Law Biosci. 2021;8(1):lsab001. Published 2021 Apr 13. doi:10.1093/jlb/lsab001
Guerrini CJ, Robinson JO, Petersen D, McGuire AL. Should police have access to genetic genealogy databases? Capturing the Golden State Killer and other criminals using a controversial new forensic technique. PLoS Biol. 2018;16(10):e2006906. Published 2018 Oct 2. doi:10.1371/journal.pbio.2006906
Ram N, Guerrini CJ, McGuire AL. Genealogy databases and the future of criminal investigation. Science. 2018;360(6393):1078-1079. doi:10.1126/science.aau1083

Presentations

2024

Christi Guerrini participated in a panel at the National Academies workshop on Law Enforcement use of Probabilistic Genotyping, Forensic DNA Phenotyping, and Forensic Investigative Genetic Genealogy Technologies in Washington DC: "Forensic Investigative Genetic Genealogy: Considerations for Implementation."

2023

Whitney Bash Brooks presented at the American Society of Bioethics and Humanities annual meeting in Baltimore, MD: "Public perceptions on law enforcement use of IGG: results from a choice experiment.
Amy McGuire and Christi Guerrini participated in an invited panel at the International Symposium on Human Identification annual meeting in Denver, CO: “Solving crimes while protecting genetic privacy.”
Whitney Bash Brooks presented two posters at the International Symposium on Human Identification annual meeting in Denver, CO: "Concerns, predictions, and possibilities: a systematic review of ethical issues associated with investigative genetic genealogy" and "Public perspectives on investigative genetic genealogy practices and policies."
Sara Huston presented a poster at the International Symposium on Human Identification annual meeting in Denver, CO:"Twitter/X insigths into public perspectives regarding investigative genetic genealogy."
Nicola Campoamor presented a poster at the Society for Medical Decision Making annual meeting in Philadelphia, PA: "Pretesting novel discrete-choice instruments: A guide for researchers."
Christi Guerrini presented at the Ramapo Investigative Genetic Genealogy Conference in Mahwah, NJ: “IGG from the inside: Practitioner Perspectives on the practice, future, and politics of investigative genetic genealogy.”
Whitney Bash-Brooks presented at the Ramapo Investigative Genetic Genealogy Conference in Mahwah, NJ: “ELSI inside the precinct: a systematic review of rthical and regulatory issues with investigative genetic genealogy.”
Diana Maden presented at the Ramapo Investigative Genetic Genealogy Conference in Mahwah, NJ: “Insights from social media into public perspectives on investigative genetic genealogy.”
Christi Guerrini presented a poster at the American Society of Crime Laboratory Directors Annual Symposium in Austin, TX: "IGG from the inside: practitioner perspectives on the practice, future, and politics of investigative genetic genealogy."

2022

Amy McGuire was a presenter in Verogen’s Forensic Investigative Genealogy Master Class webinar: “Public perceptions and Investigative Genetic Genealogy.”
Christi Guerrini presented at the at the American Society for Bioethics and the Humanities annual conference (virtual): “Investigative genetic genealogy from the inside: what is its ethical practice and future?”
Stephanie Malia Fullerton, Christi Guerrini, and Amy McGuire participated in a panel at ELSICon (virtual): “Developing an evidence base for investigative genetic genealogy policy making.”

2021

Christi Guerrini presented at The Biology of Genomes conference (virtual): “Law enforcement use of genetic data: old, new, and non controversies."

Supplement Project

IGG on the Internet: Characterizing Public Perspectives on Law Enforcement Use of Genetic Genealogy Data in Social Media

Project Description

Since DeAngelo’s arrest, IGG has aided resolution of hundreds of cases in the United States. The use of IGG has stimulated U.S. public debate about the technique’s ethical acceptability, especially important as more law enforcement use IGG in investigations.

Traditional media websites and social media platforms are a rich repository of these conversations. Specifically, public comments posted to these web platforms can be mined using informatics tools and interpreted using traditional social science methods to reveal features, applications, and consequences of IGG that are associated with public approval and disapproval. These publicly sourced data emerge without intervention or influence by researchers, allowing unique observations.

The Precision Medicine for Alzheimer’s Disease and Related Dementias Project is a joint project conducted in collaboration with the Center for Alzheimer’s and Neurodegenerative Disease at 7m��Ƶ. This project aims to integrate precision medicine (cognitive testing, genomic testing, and neuroimaging) into Alzheimer’s research and care to increase early detection of ADRD and improve clinical outcomes. In this project, at-risk patient-participants enroll together with study partners (potential caregivers) to receive cognitive testing, genetic testing, and neuroimaging (MRI, PET), and a comprehensive profile of their risk of developing ADRD. In conjunction with CAND, the Center for Medical Ethics and Health policy is assessing the impact of precision medicine testing and disclosure on both patient-participants and their potential caregivers in order to facilitate ethical and effective implementation of precision medicine disclosure.

The AD Project is enrolling 250 patient-participants and their study partners in the Houston area. The diverse settings of the study allow us to evaluate the impact of precision medicine on a diverse community, including both English and Spanish-speaking populations.

We are exploring impact across a variety of dimensions including:

Attitudes towards different testing modalities, and the perceived relative importance of different test results for future planning.
Psychological impact of testing, including both patient-participant and study partner worry and self-efficacy around test results, as well as the effects of disclosure of patient-participant results on study partner burden.
How results are actually used to improve patient-participant health behaviors for the purposes of improving ADRD outcomes.

Patient-participants and study partners complete pre-disclosure surveys to assess their expectations around results prior to receiving them. At follow-up, both patient-participants and study partners provide information about their understanding of and reaction to their results. Study partners also provide information about their caregiver burden and gains in dementia caregiving.

Supported by: a private foundation

Publications

Stevens Smith et al., , Journal of Alzheimer’s Disease

Presentation

Levchenko et al., Impact of Precision Medicine on Patient and Caregiver Perceptions of Alzheimer’s Disease. American Society for Bioethics and Humanities Annual Conference. October 2023.

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Completed Projects

Building on the previous success of the BASIC3 study, over four years, KidsCanSeq enrolled 627 pediatric patients and their parents at several diverse healthcare setting across Texas. The diverse settings of the study allowed us to evaluate our novel, culturally sensitive approaches to the informed consent process – including informational videos in English and Spanish - and return of results that includes communicating complex genomic information to families and physicians.

Supported by: U01HG006485, National Human Genome Research Institute, National Cancer Institute, NIH

Building on the previous success of the BASIC3 study, over four years, KidsCanSeq is enrolling 1100 pediatric patients and their patients at several diverse healthcare setting across Texas. The diverse settings of the study allow us to evaluate our novel, culturally sensitive approaches to the informed consent process – including informational videos in English and Spanish - and return of results that includes communicating complex genomic information to families and physicians.

We are exploring utility from a broad range of perspectives including:

testing to impact treatment decisions, and the impact of germline diagnostic and/or actionable findings on surveillance and testing recommendations for family members.
, including clinical and personal utility of the ES information.
of the ES information.

Parents complete longitudinal surveys to assess their perceived utility of and feelings about their child’s genomic results. At follow-up, parents also provide information about whether other family members followed up on any testing and surveillance recommendations, as well as barriers to doing so. Oncologists enrolled in the study complete multiple surveys to assess the clinical utility of genomic testing and its effect on treatment decisions, as well as their perceived utility of the information.

Supported by: U01HG006485, National Human Genome Research Institute and National Cancer Institute, NIH

Supplement Project: Measuring Perceptions of Utility of Clinical Genome Sequencing: Instrument Development and Validation

Project Description

A major goal of the CSER consortium is to generate evidence regarding the utility of genomic sequencing (GS). Specifically, the aim is to understand what clinical utility (e.g., impact on diagnosis, treatment, and management) and other dimensions of utility beyond those captured in medical records (e.g., psychological and pragmatic utility) clinicians, patients, families and society experience with GS information. We are developing a survey instrument to assess patients' and families' perceived utility using a rigorous methodological approach in order to generate comprehensive evidence of the broad dimensions of utility of GS. To develop this survey instrument, we are:

Developing a typology of how different stakeholders define utility through a systematic literature review. Conducting interviews with adult patients and parents of pediatric patients who received GS across diverse clinical settings that comprise the CSER consortium studies (n=60, 10 at each of 6 sites). Triangulating data from the typology and interviews to develop a comprehensive conceptual model of the relevant dimensions of perceived patient utility. This model will guide the generation of an item pool for survey instrument development that will be refined and pilot tested according to established practices for measuring patient-reported outcomes and instrument development.

Supported by: U01HG006485-S1, National Human Genome Research Institute, NIH

Publications

Gutierrez AM, Robinson JO, Raesz-Martinez R, Canfield I, Majumder MA, Scollon S, Desrosiers LR, Hsu RL, Allen-Rhoades W, Parsons DW, Plon SE, McGuire AL, Malek J. Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research. J Adolesc Young Adult Oncol. 2023 Oct;12(5):773-781. doi: 10.1089/jayao.2022.0066. Epub 2023 Jan 2. PMID: 36595372; PMCID: PMC10611971.

Muenzen KD, Amendola LM, Kauffman TL, Mittendorf KF, Bensen JT, Chen F, Green R, Powell BC, Kvale M, Angelo F, Farnan L, Fullerton SM, Robinson JO, Li T, Murali P, Lawlor JMJ, Ou J, Hindorff LA, Jarvik GP, Crosslin DR. Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience. HGG Adv. 2022 May 20;3(3):100120. doi: 10.1016/j.xhgg.2022.100120. PMID: 35707062; PMCID: PMC9190054.

Kraft SA, Russell H, Bensen JT, Bonini KE, Robinson JO, Sahin-Hodoglugil N, Renna K, Hindorff LA, Kaufman D, Horowitz CR, Waltz M, Zepp JM, Knight SJ. Conducting clinical genomics research during the COVID-19 pandemic: Lessons learned from the CSER consortium experience. Am J Med Genet A. 2022 Nov 7. doi: 10.1002/ajmg.a.63033. Epub ahead of print. PMID: 36341765.

Goddard KAB, Angelo FAN, Ackerman SL, et al. Lessons learned about harmonizing survey measures for the CSER consortium. Journal of Clinical and Translational Science. 2020;4(6):537-546. doi:10.1017/cts.2020.41.

Smith HS, Brothers KB, Knight SJ, Ackerman SL, Rini C, Veenstra DL, McGuire AL, Wilfond BS, Malek J. Conceptualization of utility in translational clinical genomics research. Am J Hum Genet. 2021 Nov 4;108(11):2027-2036. doi: 10.1016/j.ajhg.2021.08.013. Epub 2021 Oct 22. PMID: 34687653; PMCID: PMC8595895.

Plon, Sharon et al. Physician recommendations after germline sequencing in pediatric cancer patients: Texas KidsCanSeq study, Genetics in Medicine, 2022. Volume 24, Issue 3, S344.

Gutierrez AM, Robinson JO, Outram SM, Smith HS, Kraft SA, Donohue KE, Biesecker BB, Brothers KB, Chen F, Hailu B, Hindorff LA, Hoban H, Hsu RL, Knight SJ, Koenig BA, Lewis KL, Lich KH, O’Daniel JM, Sasaki SO, Tomlinson GE, Waltz M, Wilfond BS, Ackerman SL, Majumder MA. Examining Access to Care in Clinical Genomic Research and Medicine: Experiences from the CSER Consortium. Journal of Clinical and Translational Science. Epub ahead of print; 2021.

Smith HS, Morain SR, Robinson JO, Canfield I, Malek J, Rubanovich CK, Bloss CS, Ackerman SL, Biesecker B, Brothers KB, Goytia CN, Horowitz CR, Knight SJ, Koenig B, Kraft SA, Outram S, Rini C, Shipman KJ, Waltz M, Wilfond B, McGuire AL. Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development. The Patient. Epub ahead of print; 2021.

Lindberg NM, Gutierrez AM, Mittendorf KF, Ramos M, Anguiano B, Angelo F, Joseph G. Challenges and Lessons Learned in Creating Accessible Study Materials for Spanish-speaking Participants in CSER Consortium Projects. Personalized Medicine. 2021 Aug; 18(5).

Horowitz CR, Orlando LA, Slavotinek AM, Peterson J, Angelo F, Biesecker B, Bonham VL, Cameron LD, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, Hindorff LA, Jarvik GP, Kaufman D, Kenny EE, Knight SJ, Koenig BA, Korf BR, Madden E, McGuire AL, Ou J, Wasserstein MP, Robinson M, Leventhal H, Sanderson SC. The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research. Am J Hum Genet. 2019 Jun 6;104(6):1088-1096. doi: 10.1016/j.ajhg.2019.04.006. Epub 2019 May 16.

Robinson JO, Wynn J, Biesecker B, Biesecker L, Bernhardt B, Brothers KB, Chung WK, Christensen KD, Green RC, Kaufman D, McGuire AL, Hart MR, Griesemer I, Patrick DL, Rini C, Veenstra D, Cronin AM, Gray SW. Psychological Outcomes Related to Exome and Genome Sequencing Result Disclosure: A Meta-Analysis of Seven Clinical Sequencing Exploratory Research (CSER) Consortium Studies. Genetics in Medicine 2019.

Amendola, L.M., Berg, J.S., Horowitz, C.R., Angelo, F., Bensen, J.T., Biesecker, B.B., Biesecker, L.G., Cooper, G.M., East, K., Filipski, K. and Fullerton, S.M., 2018. The clinical sequencing evidence-generating research consortium: integrating genomic sequencing in diverse and medically underserved populations. The American Journal of Human Genetics, 103(3), pp.319-327.

Presentations

Malek J, Robinson J, Smith HS, Gutierrez A, Classen S, Scollon S, Parsons DW, Plon S, McGuire A. How useful is genome sequencing to parents of pediatric cancer patients? Findings from the Texas KidsCanSeqStudy. ELSIcon2022: Innovating for a Just and Equitable Future. (2022).

Gutierrez A, Robinson J, Recinos A, Desrosiers L, Majumder M, Scollon S. Families’ experiences accessing follow-up care after receiving significant germline results through a pediatric cancer research study. ELSIcon2022: Innovating for a Just and Equitable Future. (2022).

Gutierrez AM, Robinson JO, Scollon S, Majumder MA, Street RL, Parsons DW, Plon SE, McGuire AL. “Spanish-preferring parents' perceptions of and satisfaction with communication in a pediatric cancer genomic setting.” American Public Health Association Annual Meeting. October 23-27, 2021.

Gutierrez AM, Robinson JO, Scollon S, Majumder MA, Street RL, Parsons DW, Plon SE, McGuire AL. “Perspectives and preferences of adolescent and young adult cancer patients related to their participation in genomic research.” American Society for Bioethics and Humanities Annual Conference. October 13-16, 2021.

Malek J, Robinson JO, Gutierrez AM, Wang T, Smith HS, Raesz-Martinez R, Scollon S, Recinos A, Majumder MA, Parsons DW, Plon SE, McGuire AL. Great Expectations: Parents’ Perceptions of Genomic Sequencing in Pediatric Cancer Patients. American Society for Bioethics and Humanities Annual Conference. October 13-16, 2021.

Malek J, Smith H, Islam R, Robinson JO, Hsu RL, Canfield I, Raesz-Martinez R, Recinos A, Scollon S, Majumder MA, Parsons DW, Plon SE, McGuire AL. Parents’ Expected Utility of Genomic Sequencing for Pediatric Cancer Patients in the Texas KidsCanSeq Study. American College of Medicine Genetics. March 17-21, 2020.

McGuire AL (Moderator), Malek J, Smith H, Brothers Kyle. Utility of Genomic Testing: A Multidisciplinary Perspective. American Society for Bioethics and Humanities Annual Meeting. Pittsburgh, PA, US. October 24-27, 2019. Accepted as panel presentation

Gutierrez AM, Robinson JO, Malek J, Majumder M, Street RL, Parsons DW, Plon SE, McGuire AL. Implications and considerations for engaging diverse participant populations in genome research: Emerging lessons from the Texas KidsCanSeq Study. American Public Health Association Annual Meeting. Philadelphia, PA, US. November 2-6, 2019. Accepted as poster presentation.

Plon S, Amendola L, Horowitz C, Joseph G. Addressing Literacy and Language to Equitably Deliver on the Promise of Precision Medicine. American College of Medical Genetics Annual Meeting. April 2-6, 2019. Workshop.

Gutierrez AM, Robinson JO, Hsu RL, Petersen DK, Malek J, Majumder MA, Street RL, Parsons DW, Plon SE, McGuire AL. The Texas KidsCanSeq Study: Enrolling Diverse Patient Populations into Genome Research. American Society for Bioethics and Humanities Annual Meeting. Anaheim, CA, US. October 18-21, 2018. Oral presentation.

Supplement Project: Adolescent and Young Adult Cancer Patients’ Attitudes toward and Decision-Making Preferences about Clinical

Project Description

The purpose of this supplement is to examine whether and how adolescent and young adult (AYA) patients with a cancer diagnosis want to be involved in decision making about genomic sequencing. Six months after receiving their genetic test results, we ask AYA patient-participants enrolled in the KidsCanSeq study to complete a 5-minute online survey about their attitudes toward and perceived utility of their results, as well as their satisfaction with the return of results process and preferences for making decisions about their study enrollment and cancer care.

Supported by: U01HG006485-S2, National Human Genome Research Institute, NIH

The BabySeq project seeks to safely test a new approach to newborn screening using whole genome sequencing. Healthy and sick newborns’ parents, and their pediatricians, will be enrolled into this study and randomized to either receive current standard newborn screening methods or undergo whole genome sequencing plus standard newborn screening methods. A genetic counselor will provide the genomic sequencing information and newborn screening results to the families and the families’ doctors.

Through quantitative longitudinal surveys, parents will be asked about the psychosocial impact of receiving genomic sequencing results and whether the information was useful to them. Physicians will be surveyed at multiple time points to assess the perceived utility of the information and whether and how the information is actually used to manage a patient’s health.

The study will focus on the long-term implications for the health of these babies, as well as the potential impact of receiving this genetic information on the parents, the child, and the family.

Supported by: U19HD077671, Eunice Kennedy Shriver National Institute of Child Health & Human Development, National Human Genome Research Institute, NIH

Publications

Green RC, Shah N, Genetti CA, et al. Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project. Am J Hum Genet. 2023;110(7):1034-1045. doi:10.1016/j.ajhg.2023.05.007

Pereira S, Gutierrez AM, Robinson JO, et al. Parents' decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project. Genet Med. 2023;25(3):100002. doi:10.1016/j.gim.2022.100002

Armstrong B, Christensen KD, Genetti CA, et al. Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study. Front Genet. 2022;13:867371. Published 2022 Apr 27. doi:10.3389/fgene.2022.867371

Pereira S, Smith HS, Frankel LA, et al. Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial. JAMA Pediatr. 2021;175(11):1132-1141. doi:10.1001/jamapediatrics.2021.2829

Schwartz TS, Christensen KD, Uveges MK, et al. Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. J Genet Couns. 2022;31(1):218-229. doi:10.1002/jgc4.1475

Ceyhan-Birsoy, O., Murry, J.B., Machini, K., Lebo, M.S., Timothy, W.Y., Fayer, S., Genetti, C.A., Schwartz, T.S., Agrawal, P.B., Parad, R.B. and Holm, I.A., 2019. Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project. The American Journal of Human Genetics, 104(1), pp.76-93.

Pereira S, Robinson JO, Gutierrez AM, Petersen D, Hsu RL, Lee CH, Schwartz TS, Holm IA, Beggs AH, Green RC, McGuire AL, for The BabySeq Project Group. Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project. Pediatrics. 2019; 143(s1): S6-S13.

Holm IA, McGuire AL, Pereira S, Rehm H, Green RC, Beggs AH, for the BabySeq Project Group. Returning a genomic result for an adult-onset condition to the parents of a newborn: Insights from the BabySeq Project. Pediatrics. 2019; 143(s1): S37-S43.

VanNoy, G.E., Genetti, C.A., McGuire, A.L., Green, R.C., Beggs, A.H., Holm, I.A. and Group, T.B.P., 2019. Challenging the Current Recommendations for Carrier Testing in Children. Pediatrics, 143(Suppl 1), p.S27.

Genetti CA, Schwartz TS, Robinson JO, VanNoy GE, Petersen D, Pereira S, Fayer S, Peoples HA, Agrawal PB, Betting WN, Holm IA, McGuire AL, Waisbren SE, Yu TW, Green RC, Beggs AH, Parad RB. Parental Interest in Genomic Sequencing of Newborns: Enrollment Experience from the BabySeq Project. Genetics in Medicine. 2018; 21(30: 622-630.

Holm IA, Agrawal PB, Ceyhan-Birsoy O, Christensen KD, Fayer S, Frankel LA, Genetti CA, Krier JB, LaMay RC, Levy HL, McGuire AL, Parad RB, Park PJ, Pereira S, Rehm HL, Schwartz TS, Waisbren SE, Yu TW, Green RC, Beggs AH. The BabySeq Project: Implementing Genomic Sequencing in Newborns. BMC Pediatrics. 2018; 18(225). https://doi.org/10.1186/s12887-018-1200-1

Murry, J.B., Machini, K., Ceyhan-Birsoy, O., Kritzer, A., Krier, J.B., Lebo, M.S., Fayer, S., Genetti, C.A., VanNoy, G.E., Timothy, W.Y. and Agrawal, P.B., 2018. Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report. Molecular Case Studies, 4(4), p.a002873.

Berg JS, Agrawal PB, Bailey DB, Beggs AH, Brenner SE, Brower AM, Cakici JA, Ceyhan-Birsoy O, Chan K, Chen F, Currier RJ, Dukhovny D, Green RC, Harris-Wai J, Holm IA, Iglesias B, Joseph G, Kingsmore SF, Koenig BA, Kwok PY, Lantos J, Leeder SJ, Lewis MA, McGuire AL, Milko LV, Mooney SD, Parad RB, Pereira S, Petrikin J, Powell BC, Powell CM, Puck JM, Rehm HL, Risch N, Roche M, Shieh JT, Veeraraghavan N, Watson MS, Willig L, Yu TW, Urv T, Wise AL. Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics. 2017;139(2): e20162252.

Ceyhan-Birsoy, O., Machini, K., Lebo, M.S., Tim, W.Y., Agrawal, P.B., Parad, R.B., Holm, I.A., McGuire, A., Green, R.C., Beggs, A.H. and Rehm, H.L., 2017. A curated gene list for reporting results of newborn genomic sequencing. Genetics in Medicine, 19(7), p.809.

Frankel LA, Pereira S, McGuire AL. . Pediatrics, 137, 2016: 24-9.

Waisbren, S.E., Bäck, D.K., Liu, C., Kalia, S.S., Ringer, S.A., Holm, I.A. and Green, R.C., 2015. In the Early Postpartum Period, Parents are Interested in Newborn Genomic Testing. Genetics in medicine: official journal of the American College of Medical Genetics, 17(6), p.501.

Select Presentations

Blout CL, Christensen KD, Smith HS, Pereira S, Robinson JO, Genetti CA, Fayer S, Betting WN, Schwartz TS, Holm, IA, Beggs, AH, McGuire, AL, Green, RC. Physician Perceived Utility and Preparedness for Newborn Genomic Sequencing: Findings from the BabySeq Project. American College of Medical Genetics Annual Meeting. April 2019, Seattle, WA. Oral presentation.

Christensen KD, Dukhovny D, Agrawal P, Genetti CA, Holm IA, Mackay Z, McGuire AL, Pereira S, Schwartz TS, Yu T, Beggs AH, Green RC, Parad R. Screening Newborns with Genomic Sequencing Increases Short-Term Downstream Health Care Costs: Preliminary Findings from the BabySeq Project. American College of Medical Genetics Annual Meeting. April 2019, Seattle, WA. Poster presentation.

Pereira S, Petersen D, Robinson JO, Frankel L, Christensen KD, Waisbren SE, Holm IA, Beggs AH, Green RC, McGuire AL. The impact of newborn genomic sequencing on families: Findings from the BabySeq Project. American Society of Human Genetics Annual Meeting. October 2018, San Diego, CA. Oral presentation.

Holm, IA, Genetti, CA, Pereira, S, Green, RC, Beggs, AH, McGuire, AL. BRCA2, ELSI, and the Return of Genomic Results in the BabySeq Project. 4th ELSI Congress, June 2017. Poster presentation.

HA Peoples, AM Gutierrez, S Pereira, JO Robinson, L Frankel, MC Towne, M Helm, CA Genetti, IA Holm, AH Beggs, RC Green, AL McGuire. Benefits, Risks, and Perceived Utility of Newborn Genomic Sequencing: Comparing Clinicians' and Physicians' Baseline Attitudes in the BabySeq Project. American Society of Human Genetics Annual Meeting. Vancouver, Canada. October 2016. Poster presentation.

Pereira S, Frankel L, Robinson JO, Weipert CM, Towne MC, Gutierrez A, Lee K, Holm IA, Dukhovny D, Beggs AH, Green RC, McGuire AL. Genomic Sequencing of Newborns: Exploring Psychosocial Risks to Families. American Society of Human Genetics Annual Meeting. Baltimore, MD. October 2015. Poster presentation.

This project is part of the NIH’s Clinical Sequencing Exploratory Research program. The project’s goal is to integrate genomic sequence data into the care of childhood cancer patients with high-risk solid tumors and brain tumors. With clinical colleagues at Texas Children’s Cancer Center and genetic scientist at BCM’s Whole Genome Laboratory, the project is assessing the impact of reporting whole exome sequence data through physicians to participating parents. The project is evaluating physician-parent communication and clinical decision-making to explore:

How the availability of tumor whole exome sequence data affects physician recommendations regarding enrollment on specific clinical trials and the treatment plans chosen in the scenario of tumor recurrence.
How the availability of germline whole exome sequence data affects cancer surveillance for patients and genetic testing and cancer surveillance for family members.

Additionally, this project will address parental understanding, preferences for receiving genomic sequence data, and ethical issues related to the appropriate use and reporting of this information, including possible incidental findings in a pediatric setting.

Supported by: U01HG006485, National Human Genome Research Institute, NIH

Publications

Scollon S, Bergstrom K, McCullough LB, McGuire AL, Gutierrez S, Kerstein R, Parsons DW, Plon SE. Pediatric cancer genetics research and an evolving preventive ethics approach for return of results after death of the subject. The Journal of Law, Medicine & Ethics. 2015 Sep;43(3):529-37.

McCullough LB, Slashinski MJ, McGuire AL, Street Jr RL, Eng CM, Gibbs RA, Parsons DW, Plon SE. Is whole‐exome sequencing an ethically disruptive technology? Perspectives of pediatric oncologists and parents of pediatric patients with solid tumors. Pediatric Blood and Cancer. 2016 Mar;63(3):511-5.

Gutierrez AM, Statham EE, Robinson JO, Slashinski MJ, Scollon S, Bergstrom KL, Street Jr RL, Parsons DW, Plon SE, McGuire AL. Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families. Patient Education and Counseling. 2019 May 1;102(5):895-901.

Scollon S, Majumder MA, Bergstrom K, Wang T, McGuire AL, Robinson JO, Gutierrez AM, Lee CH, Hilsenbeck SG, Plon SE, Parsons DW. Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents. Patient Education and Counseling. 2019 Apr 1;102(4):680-6.

Malek J, Pereira S, Robinson JO, Gutierrez AM, Slashinski MJ, Parsons DW, Plon SE, McGuire AL. Responsibility, culpability, and parental views on genomic testing for seriously ill children. Genetics in Medicine. 2019 Dec;21(12):2791-7.

Hsu RL*, Gutierrez AM*, Schellhammer SK, Robinson JO, Scollon S, Street Jr RL, Salisbury AN, Pereira S, Malek J, Parsons DW, Plon SE, McGuire AL. “Pediatric oncologists’ experiences returning and incorporating genomic sequencing results into cancer care.” Journal of Personalized Medicine. 2021 Jun; 11(6): 570. *These authors contributed equally to this work.

Gutierrez AM, Robinson JO, Statham EE, Scollon S, Bergstrom KL, Slashinski MJ, Parsons DW, Plon SE, McGuire AL, Street RL. Portero versus . Personalized Medicine 14(6), 2017: 503-514.

Malek, J, M Slashinski, JO Robinson, Gutierrez AM, Parsons DM, Plon SE, McCullough LB, McGuire AL. . Journal of Clinical Oncology: Precision Oncology, 2017. [Epub ahead of print]

Parsons DW, Roy A, Yang Y, Wang T, Scollon S, Bergstrom K, Kerstein RA, Gutierrez S, Petersen AK, Bavle A, Lin FY, López-Terrada DH, Monzon FA, Hicks MJ, Eldin KW, Quintanilla NM, Adesina AM, Mohila CA, Whitehead W, Jea A, Vasudevan SA, Nuchtern JG, Ramamurthy U, McGuire AL, Hilsenbeck SG, Reid JG, Muzny DM, Wheeler DA, Berg SL, Chintagumpala MM, Eng CM, Gibbs RA, Plon SE. . JAMA, 2016. [Epub ahead of print]

Scollon S, Bergstrom K, Kerstein R, Wang T, Hilsenbeck SG, Ramamurthy U, Gibbs RA, Eng CM, Chintagumpala MM, Berg SL, McCullough LB, McGuire AL, Plon SE, Parsons DW. . Genome Medicine, 6(9), 2014: 69.

Clayton EW, McCullough LB, Biesecker LG, Joffe S, Ross LF, Wolf SM, for the Clinical Sequencing Exploratory Research (CSER) Consortium Pediatrics Working Group.. Am J Bioeth, 14(3), 2014: 3-9.

McGuire AL, Joffe S, Koenig BA, Biesecker BB, McCullough LB, Blumenthal-Barby JS, Caulfield T, Terry SF, Green RC. . Science, 340, 2013: 1047-1048.

McGuire AL, Robinson JO, Ramoni RB, Morley DS, Joffe S, Plon SE. . Personalized Medicine, 10(1), 2013: 27-34.

Ramoni RB, McGuire AL, Robinson JO, Morley DS, Plon SE, Joffe S. . Genetics in Medicine, 15(11), 2013: 882-887.

McGuire AL, McCullough LB, Evans JP. . JAMA, 309, 2013: 1465-1466.

Presentations

Hsu RL, Gutierrez AM, Schellhammer S, Robinson JO, Pereria S, Scollon S, Malek J, Parsons DW, Plon SE, McGuire AL. Was Implementing Genomic Sequencing in Pediatric Cancer Care Disruptive? Oncologists’ Views After Returning Genomic Results in The BASIC3 Study. American College of Medicine Genetics. March 17-21, 2020. Poster Presentation.

Gutierrez AM, Robinson JO, Slashinski MJ, Statham EE, Street RL, Parsons DW, Plon SE, McGuire AL, McCullough LB. More than Just Translation: The Role of Medical Interpreters in the Disclosure of Whole Exome Sequencing Results for Spanish-Speaking Families. American Society for Bioethics and Humanities Annual Conference. Washington, DC. October 2016.

Malek, J. Culpability and Responsibility in Parents’ Experiences with Genome Sequencing for Pediatric Cancer Patients. American Society for Bioethics and Humanities Annual Conference. Washington, DC, October 2016.

Malek, J. Parental Perspectives on Whole Exome Sequencing in Pediatric Cancer: A Typology of Perceived Utility. American Society of Human Genetics Annual Meeting. Vancouver, CA, October 2016.

Gutierrez AM, Robinson JO, Statham EE, Slashinski MJ, Scollon S, Bergstrom KL, Street RL, Parsons DW, Plon SE, McGuire AL, McCullough LB. Lost in Translation: How Medical Interpreters Modify the Communication of Whole Exome Sequencing Results during Translation for Spanish-Speaking Families. National Society of Genetic Counselors Annual Education Conference. Seattle, WA. September/October 2016. Poster Presentation.

McCullough LB, Slashinski MJ, Wycliff J, McGuire AL, Street Jr. RL, Parsons DW, Plon SE. Do Pediatric Oncologists and Parents Experience Whole Exome Sequencing of Solid Organ Tumors in Children as a Disruptive Technology? The American Society for Bioethics and Humanities Annual Meeting, San Diego, CA. October 2014.

Many national and international public and private initiatives are forming to collect and share data on a large scale for research and clinical use. Collectively, these efforts may lead to the creation of a medical information commons.

Through this project, we aimed to inform policy decisions about effective governance for data sharing, and ensure that the values, rights and interests of individuals whose data may populate the information commons are represented. Specifically we aimed to:

Identify and analyze existing models for collecting diverse sources of data into a medical information commons to enable large scale research and clinical application
Evaluate the effectiveness of existing models and develop new approaches to address key policy issues from the perspective of expert stakeholders
Solicit informed public input on existing models and innovative approaches from individuals whose data may populate a medical information commons.
Describe incentives to share BRCA variant data and obstacles hindering the sharing of those data, and incorporate BRCA previvors and survivors into the governance and oversight structures for the emergent BRCA data commons.

Over the past four years, we carried out the following:

A landscape analysis of existing data-sharing efforts
In-depth interviews with multiple stakeholders from various sectors (e.g., academia, government, and private industry)
Deliberative sessions with members of the public at three U.S. cities
In-person meetings with a multidisciplinary external advisory committee

Supported by: DI-2017C2-7726, Patient-Centered Outcomes Research Institute

Special Issue in the Journal of Law, Medicine & Ethics

Where scientists and ethicists look to address and propose solutions to many of the questions that surround medical data sharing.

Publications

Bollinger JM, Sanka A, Dolman L, Liao RG, Cook-Deegan R. BRCA1/2 Variant Data-Sharing Practices. J Law Med Ethics. 2019;47(1):88-96. doi:10.1177/1073110519840487

Deverka PA, Gilmore D, Richmond J, et al. Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons. J Law Med Ethics. 2019;47(1):70-87. doi:10.1177/1073110519840486

McGuire AL, Roberts J, Aas S, Evans BJ. Who Owns the Data in a Medical Information Commons? J Law Med Ethics. 2019;47(1):62-69. doi:10.1177/1073110519840485

Majumder MA, Bollinger JM, Villanueva AG, Deverka PA, Koenig BA. The Role of Participants in a Medical Information Commons. J Law Med Ethics. 2019;47(1):51-61. doi:10.1177/1073110519840484

Bollinger JM, Zuk PD, Majumder MA, et al. What is a Medical Information Commons? J Law Med Ethics. 2019;47(1):41-50. doi:10.1177/1073110519840483

Villanueva AG, Cook-Deegan R, Robinson JO, McGuire AL, Majumder MA. Genomic Data-Sharing Practices. J Law Med Ethics. 2019;47(1):31-40. doi:10.1177/1073110519840482

Villanueva AG, Cook-Deegan R, Koenig BA, et al. Characterizing the Biomedical Data-Sharing Landscape. J Law Med Ethics. 2019;47(1):21-30. doi:10.1177/1073110519840481

McGuire AL, Majumder MA, Villanueva AG, et al. Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons. J Law Med Ethics. 2019;47(1):12-20. doi:10.1177/1073110519840480

Cook-Deegan R, Majumder MA, McGuire AL. Introduction: Sharing Data in a Medical Information Commons - Robert Cook-Deegan, Mary A. Majumder, Amy L. McGuire, 2019. The Journal of Law, Medicine & Ethics. 2019;47(1):7-11.

Majumder MA, Zuk PD, McGuire AL. J, Cole D, eds. Routledge Handbook of the Study of the Commons. 1st ed.

Deverka PA, Majumder MA, Villanueva AG, et al. Creating a data resource: what will it take to build a medical information commons? Genome Med. 2017;9(1):84. doi:10.1186/s13073-017-0476-3

Majumder MA, Guerrini CJ, Bollinger JM, Cook-Deegan R, McGuire AL. Sharing data under the 21st Century Cures Act. Genet Med Off J Am Coll Med Genet. May 2017. doi:10.1038/gim.2017.59

Cook-Deegan R, McGuire AL. Moving beyond Bermuda: sharing data to build a medical information commons. Genome Res. 2017;27(6):897-901. doi:10.1101/gr.216911.116

Majumder MA, Cook-Deegan R, McGuire AL. Beyond Our Borders? Public Resistance to Global Genomic Data Sharing. PLoS Biol. 2016;14(11):e2000206. doi:10.1371/journal.pbio.2000206

Presentations

Majumder MA. Back to the Future: A Snapshot of Current Genomic Data-Sharing Practices. Presented at the: American Society for Bioethics and Humanities Annual Conference; October 2018; Anaheim, CA.

Majumder MA. What Role for Participants? Views of Expert Stakeholders Influencing Data-Sharing Policies and Practices. Presented at the: American Society for Bioethics and Humanities Annual Conference; October 2017; Kansas City, MO.

Villanueva AG. The Challenges of Collecting and Sharing Environmental Data in the Current Genomics Era. Poster presented at the: American Society for Bioethics and Humanities Annual Conference; October 2017; Kansas City, MO.

Villanueva AG. Hashtag Who's Missing? Lessons for Participant-Centric and Pediatric Genomic Databases. Presented at the: ELSI Congress; June 2017; Farmington, CT.

McGuire AL. What Does it Mean to Own the Data in a Medical Information Commons? Presented at the: ELSI Congress; June 2017; Farmington, CT.

Villanueva AG. The Data Ecosystem: Current Data-Sharing Policies and Practices. Presented at the: ELSI Congress; June 2017; Farmington, CT.

Majumder MA. Big data sharing in precision medicine. Presented at the: World precision Medicine Congress; May 2017; London, UK.

Majumder MA, Garrison NA, Bonham V, Villanueva AG. Critical Distance in ELSI Genomics Research - More Than Advocacy for the "All-Frills Yuppie Health Care Boutique"? Presented at the: American Society for Bioethics and Humanities Annual Conference; October 2016; Washington, DC.

McGuire AL, Goldstein MM, Rodriguez LL, O'Donnell CJ. Building a Medical Information Commons: Ethical, Policy and Practical Challenges. Presented at the: American Society for Bioethics and Humanities Annual Conference; October 2016; Washington, DC.

Villanueva AG, McGuire AL, Majumder MA. Genes and the Environment: Current Data Collection, Sharing and Privacy Protection Practices. Poster presented at the: American Public Health Association's Annual Meeting; November 2016; Denver, CO.

McGuire AL. Building the Medical Information Commons: Data Sharing Ethics and Policy. Human Genome Meeting; 2016; Houston, TX.

The MedSeq Project is one of the nine projects funded by the NIH’s Clinical Sequencing Exploratory Research program. MedSeq is exploring and comparing the impact of using whole genome sequencing (WGS) in two distinct clinical settings, primary care and cardiology. This randomized controlled trial is enrolling primary care physicians and their healthy, middle-aged patients, and cardiologists and their patients presenting with cardiomyopathy. Enrolled patients are randomly assigned to either undergo WGS or receive current standard of care.

Major goals of the project include creating standards for genetic variant disclosure to physicians and their patients, a careful examination of the preferences and motivations of physicians and patients enrolled, evaluating the flow and utilization of genomic information within the clinical interactions, and assessing the understanding, behavior, medical consequences and healthcare costs associated with the use of WGS in these models of medical practice.

Supported by: U01HG006500, National Human Genome Research Institute, NIH

Publications

Roberts JS, Robinson JO, Diamond PM, Bharadwaj A, Christensen KD, Lee KB, Green RC, McGuire AL. . Genet Med. 2018. [Epub ahead of print]

Vassy JL, Davis JK, Kirby C, Richardson IJ, Green RC, McGuire AL, Ubel PA. J Gen Intern Med. 2018. [Epub ahead of print]

Robinson JO, Carroll TM, Feuerman LZ, Perry DL, Hoffman-Andrews L, Walsh RC, Christensen KD, Green RC, McGuire AL. J Empir Res Hum Res Ethics 11(1), 2016: 21 - 30.

Lupo PJ, Robinson JO, Diamond PM, Jamal L, Danysh HE, Blumenthal-Barby J, Lehmann LS, Vassy JL, Christensen KD, Green RC, McGuire AL. Per Med, 13(1), 2016: 13-20.

Christensen KD, Vassy JL, Jamal L, Lehmann LS, Slashinski MJ, Perry DL, Robinson JO, Blumenthal-Barby J, Feuerman LZ, Murray MF, Green RC, McGuire AL. . Clin Genet, 89(2), 2016: 228-34.

Vassy JL, Christensen KD, Slashinski MJ, Lautenbach DM, Raghavan S, Robinson JO, Blumenthal-Barby J, Feuerman LZ, Lehmann LS, Murray MF, Green RC, McGuire AL. . Per Med, 12(1), 2015: 23-32.

Green RC, Lautenbach D, McGuire AL. . N Engl J Med, 372(5), 2015: 397-399.

Vassy JL, McLaughlin HL, MacRae CA, Seidman CE, Lautenbach DM, Krier J, Lane WJ, Kohane IS, Murray MF, McGuire AL, Rehm HL, Green RC. . Public Health Genomics, 18(2), 2015: 123-129.

Blumenthal-Barby JS, McGuire AL, Green RC, Ubel PA. . Genome Med, 7(1), 2015: 13.

Blumenthal-Barby JS, McGuire AL, Ubel PA. . Ann Intern Med, 161(8), 2014: 605-606.

Vassy JL, Lautenbach DM, McLaughlin HM, Kong SW, Christensen KD, Krier J, Kohane IS, Feuerman LZ, Blumenthal-Barby J, Roberts JS, Lehmann LS, Ho CY, Ubel PA, MacRae CA, Seidman CE, Murray MF, McGuire AL, Rehm HL, Green RC. . Trials, 15(1), 2014: 85.

Gray SW, Martins Y, Feuerman LZ, Bernhardt BA, Biesecker BB, Christensen KD, Joffe S, Rini C, Veenstra D, McGuire AL. . Genetics in Medicine 16(10), 2014: 727-735.

McGuire AL, Joffe S, Koenig BA, Biesecker BB, McCullough LB, Blumenthal-Barby JS, Caulfield T, Terry SF, Green RC. . Science, 340, 2013: 1047-1048.

Green RC, Berg JS, Grody WW, Kalie SS, Korf BR, Marin CL, McGuire AL, et al. . Genetics in Medicine 15(7), 2013: 565-574.

McGuire AL, McCullough LB, Evans JP. . JAMA, 309, 2013: 1465-1466.

Lewis MH, Scheurer ME, Green RC, McGuire AL. . Science Translational Medicine, 4(159), 2012: 159cm12.

Green RC, Berg JS, Berry GT, Biesecker LG, Dimmock D, Evans JP, Grody WW, Hegde M, Kalia S, Korf BR, Krantz I, McGuire AL, Miller DT, Murray MF, Nussbaum R, Plon SE, Rehm HL, Jacob HJ. . Genetics in Medicine, 14(4), 2012: 405-410.

Presentations

Christensen KD, Lupo P, Robinson JO, Blumenthal-Barby J, Vassy JL, Lehmann LS, Ubel PA, Roberts JS, Green RC, McGuire AL. Patient Perceptions about the Utility of Family History Review during Whole Genome Sequencing: Initial Findings from the MedSeq Study. The American Society of Human Genetics Annual Meeting, San Diego, CA. October 2014.

Vassy JL, Davis K, Robinson JO, Blumenthal-Barby J, Christensen KD, Green RC, McGuire AL, Ubel PA for the MedSeq Project. Contextualization and Recommendation: How Doctors and Patients Discuss Whole-Genome Sequencing and Results. The American Society of Human Genetics Annual Meeting, San Diego, CA. October 2014.

Jamal L, Robinson JO, Lupo P, Blumenthal-Barby J, Feuerman LZ, Vassy JL, Christensen KD, Slashinski MJ, Wycliff J, Green RC, McGuire AL for the MedSeq Project. Patients’ Perceptions of Whole Genome Sequencing Results and Plans to Use Non-Actionable Findings. The American Society of Human Genetics Annual Meeting, San Diego, CA. October 2014. The American Society for Bioethics and Humanities Annual Meeting, San Diego, CA. October 2014. The National Society of Genetic Counselors Annual Education Conference, New Orleans, LA. September 2014.

McGuire A, Henderson G, Gray S, Rini C, Bernhardt B. Whole Genome/Exome Sequencing: Patient Expectations, Literacy, and Preferences for Genome Information. The American Society of Human Genetics Annual Meeting, San Diego, CA. October 2014.

Vassy JL, Christensen KD, Slashinski MJ, Lautenbach D, Robinson JO, Blumenthal-Barby J, Feuerman LZ, Green RC, McGuire AL. "Someday it will be the Norm:" Physician Perceptions of the Clinical Utility of Whole Genome Sequencing. Society of General Internal Medicine National Meeting, San Diego, CA. April 2014.

Carroll T, Robinson JO, Feuerman LZ, Lautenbach DM, Green RC, McGuire AL. ELSI Concerns of Participants and Decliners in the MedSeq Project: A Randomized Trial of Whole Genome Sequencing. The National Conference on Undergraduate Research, Lexington, KY. April 2014. The American College of Medical Genetics Annual Meeting, Nashville, TN. March 2014.

Christensen KD, Green RC, Vassy JL, Murray MF, McGuire AL. "Somebody Translate this Information for Me:" Physician Perceptions of their Preparedness to Disclose Full Genome Sequencing Results. The American College of Medical Genetics Annual Meeting, Nashville, TN. March 2014.

Enabling Personalized Medicine through Exome Sequencing in the U.S. Air Force (the MilSeq Project) is a pilot study examining the process of incorporating genome sequencing (GS) into the United States Air Force (USAF) military health system. Active-duty service members of the USAF (Airmen) are enrolled into the study to undergo GS. Results are returned directly to Airmen by military healthcare providers who are also study participants, and are placed in their electronic health records by the study genetic counselor. 7m��Ƶ providers participate in an education session about genomic medicine and are supported by the study genetic counselor.

Through pre- and post-disclosure surveys, we ask Airmen about their motivations and barriers to undergoing GS, the impact of receiving their sequencing results, and their thoughts on integrating this type of information into the USAF military health system. 7m��Ƶ providers complete surveys about the genomic education session, their genetic knowledge and feelings of preparedness to communicate this information, and their perceived utility of the information. We are also assessing how the information is used to inform the management of the Airmen’s health.

We are interested in gaining knowledge about the barriers to and medical, behavioral, and economic implications of implementing genomic sequencing information into clinical care in the military health system through the perspectives of USAF Airmen and healthcare providers.

Supported by: FA8650-17-2-6704, U.S. Department of Defense

Disclaimer

This material is based on research sponsored by Air Force Medical Support Agency, Research and Acquisition Directorate AFMSA/SG5 under cooperative agreement number FA8650-17-2-6704. The U.S. Government is authorized to reproduce and distribute reprints for Governmental purposes notwithstanding any copyright notation thereon.

The views and conclusions contained herein are those of the authors and should not be interpreted as necessarily representing the official policies or endorsements, either expressed or implied, of Air Force Medical Support Agency, Research and Acquisition Directorate AFMSA/SG5 or the U.S. Government.

The voluntary, fully informed consent of the subjects used in this research was obtained as required by 32 CFR 219 and AFI 40-402, Protection of Human Subjects in Biomedical and Behavioral Research.

Publications

De Castro M, Biesecker L, Turner C, Brenner R, Witkop C, Mehlman M, Bradburne, Green RC. Genomic Medicine in the Military. Genomic Medicine. 2016: 1:15008.

Presentations

Hsu RL, Pereira S, Robinson JO, Islam R, Majumder M, Parasidis E, Mehlman MJ, Christensen K, Maxwell MD, Blout C, Lebo M, Killian JK, De Castro M, Green RC, McGuire AL. US Air Force Airmen's Perceptions after Receiving Genome Sequencing: Preliminary Results from the MilSeq Project. American Society for Bioethics and Humanities Annual Meeting. Pittsburgh, PA, US. October 24-27, 2019. Accepted as oral presentation.

Blout CL, Sirotich E, Zoltick E, Christensen K, Robinson JO, Pereira S, Petersen DK, Maxwell MD, Gardner C, De Castro M, Lebo M, McGuire AL, Brenner R, Green, RC. Healthy Genomic Sequencing: What Airmen Want to Know? Findings from the MilSeq Project. National Society of Genetic Counselors Annual Meeting. Atlanta, GA, US. November 14-17, 2019. Poster presentation.

Pereira S, Robinson JO, Hsu, RL, Petersen DK, Majumder MA, Parasidis E, Mehlman MJ, Christensen KD, Maxwell MD, Blout CL, Lebo M, Brenner R, Gardner C, De Castro M, Green RC, McGuire AL. Airmen's Attitudes Toward Genomic Sequencing In The US Air Force: Results From The Milseq Project. American Society for Bioethics and Humanities Annual Meeting. Anaheim, CA, US. October 18-21, 2018. Oral presentation.

Hsu RL, Pereira S, Robinson JO, Petersen JK, Majumder M, Parasidis E, Mehlman M, Christensen K, Maxwell MD, Blout C, Lebo M, Brenner R, Gardner C, De Castro M, Green RC, McGuire AL. Airmen's Attitudes toward Genomic Sequencing in the US Air Force: Results from The MilSeq Project. American Society for Human Genetics Annual Meeting. San Diego, CA, US. October 16-20, 2019. Poster presentation.

Maxwell, MD. Robinson JO, Gardner CL, De Castro M, Lebo M, Blout CL, Vassy JL, Christensen KD, Krier JB, Pereira S, McGuire AL, Mehlman MJ, Parasidis E, Brenner R, Green RC. Pharmacogenomics in the US Air Force: Development of a Tailored Panel for the MilSeq Project. American College of Medical Genetics and Genomics. Charlotte, NC. April 2018.

Press Release

, Genomeweb Clinical Sequencing. October 2017.

The PeopleSeq Consortium, funded by the NIH, is conducting a longitudinal study of healthy adults by surveying those who plan to, or have already received, their own genomic sequence information. Genomic sequencing, including genome sequencing (GS) and exome sequencing (ES), are available to and being utilized by physicians and their patients in both research and clinical settings. The use of genomic sequencing in healthy populations to screen for disease variants is conceptually different from anything practiced today in medical genetics. Instead of using genomic technology in the hopes of identifying a cause for a specific condition, genomic sequencing in healthy individuals would follow a model of “predispositional" genomic testing. Genomic sequencing of healthy individuals could grow to resemble current population-based preventative screening measures, such as newborn screening (the "heel price" test).

PeopleSeq participants have received their GS information through various commercial and research avenues, many of which follow different return of results models. Our longitudinal surveys focus on the medical, behavioral, and economic impact of performing genomic sequencing in healthy adults, and were built by drawing upon our prior experience in designing and implementing rigorous studies of the outcomes of genetic testing and results disclosure, including the Study and the MedSeq Project.

We are also conducting interviews with participants who received unanticipated disease risk results to explore the impact of this information, and participant's decision making processes, informational needs, and sharing preferences after receiving such information.

Despite the promise of genomic sequencing for personalized medicine, there remain significant challenges and concerns that must be addressed. Some consider the utilization of genomic sequencing in healthy individuals to be controversial; the short and long-term outcomes of providing genomic sequencing information to healthy adults are not yet known.

The PeopleSeq Consortium enables us to collect valuable empirical data on the medical, behavioral, and economic impact of performing genomic sequencing in healthy adults.

Supported by: R01-HG009922, R01HG011268, National Human Genome Research Institute, NIH

Participating Institutes in the PeopleSeq Consortium

Genomes2People
PeopleSeq Scientific Team
7m��Ƶ
GeneDx
Genos/NantOmics
Harvard Personal Genome Project
HudsonAlpha Institute for Biotechnology
Illumina
Invitae
Mayo Clinic
Mt. Sinai School of Medicine
OpenSNP
*PerkinElmer
SoundRocket/Survey Sciences Group
University of Vermont
*Veritas Genetics
*Formal affiliation pending

View more detailed information about the or email us at peopleseq@partners.org.

Publications

Zoltick, E.S., Linderman, M.D., McGinniss, M.A., Ramos, E., Ball, M.P., Church, G.M., Leonard, D.G., Pereira, S., McGuire, A.L., Caskey, C.T. and Sanderson, S.C., 2019. Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium. Genome medicine, 11(1), p.10.

Linderman, M., Nielsen, D. and Green, R., 2016. Personal genome sequencing in ostensibly healthy individuals and the PeopleSeq Consortium. Journal of personalized medicine, 6(2), p.14.

Presentations

Zoltick, ES, Linderman, MD, Nielsen, DE, Betting, WN, McGinniss, MA, Ramos, E, Ball, MP, Leonard, DGB, Pereira, S, Sanderson, SS, Crawford, SD, Green, RC, the PeopleSeq Consortium. Temporal Differences in Concerns, Motivations, and Attitudes regarding Predispositional Genome Sequencing among Healthy Adults: Findings from the PeopleSeq Consortium. Poster presented at the American Society of Human Genetics Annual Meeting, October 2018, San Diego, CA.

Sutti, S, Zotick, E, Linderman, M, Nielsen, D, McGinnis, M, Ramos, E, Ball, M, Leonard, D, Pereira, S, Sanderson, S, Crawford, S, Green, RC. Participant Perspectives in Discussing Predispositional Genome Sequencing Results with 7m��Ƶ Providers: Findings from the PeopleSeq Consortium. Poster presented at the American College of Medical Genetics and Genomics Annual Meeting, April 2018, Charlotte, NC.

Zoltick, E, Linderman, M, Nielsen, D, McGinnis M, Ramos, E, Ball, M, Leonard, D, Pereira, S, Sanderson, S, Crawford, S, Green, RC. Motivations, Outcomes, and Attitudes Following Predispositional Genome Sequencing among 7m��Ƶ Professionals and Non-7m��Ƶ Professionals: Findings from the PeopleSeq Consortium. Poster presented at the American College of Medical Genetics and Genomics Annual Meeting, April 2018, Charlotte, NC.

Green RC, Hambuch T, Ball M, Church G, Linderman M, Pearson N, Roberts JS, Sanderson S, Weipert C, Helm M, Schadt E. Predispositional Genome Sequencing in Healthy Adults: Preliminary Findings from the PeopleSeq Study. American College of Medical Genetics Annual Meeting. Salt Lake City, UT, US. March 24-28, 2015. Poster presentation.

The clinical integration of next generation sequencing (NGS) has brought to light challenging policy concerns such as oversight of test quality and services, patenting and licensing issues, privacy and data sharing, and insurance coverage and reimbursement. A team of legal and policy experts came together to identify, prioritize and deliberate the most important and tractable policy barriers and solutions to the clinical adoption of NGS.

This involved three major research activities:

Landscape analysis of current and emerging NGS companies and qualitative interviews with industry leaders, to understand how the industry is developing in an uncertain policy climate ( and check out the list of next generation sequencing companies we developed using crowdsourcing methods).
Legal analysis of key policy issues related to regulation, reimbursement, intellectual property and data sharing ().
Modified Delphi process involving a series of four surveys to identify and prioritize the unique policy challenges involved in translating the health benefits of NGS ().

Supported by: R01HG006460, National Human Genome Research Institute, NIH

Publications

Guerrini CJ, McGuire AL, Majumder MA, Bollinger JS, Rowan PJ. J. Law & Biosciences 4(3), 2017: 542-564.

Guerrini CJ, McGuire AL, Majumder MA. Science 356(6338), 2017: 586-587.

Curnutte MA, Frumovitz KL, Bollinger JM, Cook-Deegan RM, McGuire AL, Kaufman DJ, Majumder MA. . Nat Biotechnol 34, 2016: 466-470.

Messner DA, Naber JA, Koay P, Cook-Deegan R, Majumder M, et al. . Appl Trans Genom 10, 2016: 19-24.

Guerrini CJ, Majumder M, McGuire AL. . Nat Biotechnol 34(2), 2016: 145-7.

Deverka PA, Kaufman D, McGuire AL. . JAMA 312(18), 2014: 1857-1858.

Special Issue for the Journal of Law, Medicine & Ethics 42(3), 2014 includes articles from:

Amy McGuire, Margaret Curnutte, and David Kaufman.
Gail Javitt and Katherine S. Carner.
Patricia Deverka and Jennifer Dreyfus.
Robert Cook-Deegan and Subhashini Chandrasekharan.
Barbara J. Evans.

Curnutte MA, Frumovitz KL, Bollinger JM, McGuire AL, Kaufman DJ. . Nature Biotechnology 32(10), 2014: 980-982.

Chandrasekharan S, McGuire AL, Van den Veyver IB. Prenatal Diagn 34(10), 2014: 921-926.

Selected Presentations

Guerrini C. The New Landscape of Patent Eligibility: Empirical Findings. BioCanRx Summit for Cancer Immunotherapy. Ottawa, ON. June 2017.

Guerrini C. The New Legal Landscape of Genomics Patents: A Qualitative Study. The American Society of Human Genetics Annual Meeting, Washington, DC. October 2016.

McGuire AL, Kaufman DJ, Javitt GH, Deverka PA, Messner D, Cook-Deegan R, Curnutte MA, Bollinger J, Dvoskin R, Chandrasekharan S, Evans BJ. Clinical Integration of NGS: A Policy Analysis. The American Society of Human Genetics Annual Meeting, San Diego, CA. October 2014.

Curnutte MA, Frumovitz KL, Bollinger J, McGuire AL, Kaufman DJ. Tracking the Development of the Clinical Next Generation Sequencing Industry. The American Society of Human Genetics Annual Meeting, San Diego, CA. October 2014.

McGuire AL. Stakeholder Views of Regulatory Issues Related to Next Generation Sequencing. Legal Issues in Genomic Medicine Session, Clinical Sequencing Exploratory Research (CSER) Meeting, Bethesda, MD. October 2014.

Curnutte MA. The Next Generation Sequencing Industry: A Critique of the Policy-Lag Narrative. 13th Annual Science & Democracy Network Meeting, Vienna, Austria, June 2014. Department of Social Science, Health & Medicine, King’s College London, United Kingdom. June 2014.

Curnutte MA. Genetic Information in Context. Center for Genomics and Society, University of North Carolina, Chapel Hill, NC. April 2014.

Curnutte MA. Development of the Clinical NGS Industry in a Shifting Policy Climate. Clinical Genetics Conference, sponsored by 7m��Ƶ, Houston, TX. April 2014.

Curnutte MA. Genetic Information is as Genetic Information Does. American Anthropological Association Annual Meeting, Chicago, IL. November 2013.

Curnutte MA, Frumovitz KL, Bollinger J, Javitt GH, Carner KS, Cook-Deegan R, Chandrasekharan S, Messner D, Deverka P, Kaufman DJ, McGuire AL. Mapping the Next Generation Sequencing Industry. The American Society of Human Genetics Annual Meeting, Boston, MA. October 2013.

Curnutte MA. Mapping the Next Generation Sequencing Industry. The Clinical Genome Conference, San Francisco, CA. June 2013.

As the whole genome sequencing industry continues to grow, it is imperative that policy challenges arising from the utilization of this technology are identified and addressed in a timely manner. Through a modified Delphi process, a methodology used to iteratively engage a diverse group of stakeholders, this project identifies and prioritizes the unique policy challenges involved in translating WGS into health benefits in the United States. Using a mixed methods approach, such as a landscape analysis of the current and emerging WGS industry and qualitative interviews with industry leaders, the study team is developing an initial list of policy questions to be distributed to key stakeholders who will help refine and prioritize the resulting issues by importance and tractability.

Returning Research Results of Pediatric Genomic Research to Participants

Returning genomic research results to participants is rife with ethical issues, especially when the research participants are children. This study explores the legal implications of returning pediatric genomic research results to participants. By using standard legal analytic tools, study investigators are developing criteria to govern the ethical return of incidental findings and results of pediatric genomic research. US laws and international guidelines regarding decision making for and by minors are included in the analysis to provide a foundation for developing these criteria.

Supported by: R21HG006612, National Human Genome Research Institute, NIH

Publications Related to Genome Law and Policy

McGuire AL, Wang MJ, Probst FJ. Identifying consanguinity through routine genomic analysis: Reporting requirements. The Journal of Law, Medicine, and Ethics. 2012; 40 (4): 1040-6.

Clayton EW, McGuire AL. The Legal Risks of Returning Results of Genomics Research. Genetics in Medicine 14(4), 2012:473-477.

McGuire AL, Joffe S, Koenig BA, Biesecker BB, McCullough LB, Blumenthal-Barby JS, Caulfield T, Terry SF, Green RC. Ethics and genomic incidental findings. Science. 2013; 340 (6136): 1047-8.

Green RC, Berg JS, Grody WW, Kalia SS, Korf BR, Martin CL, McGuire AL, Nussbaum RL, O’Daniel JM, Ormond KE, Rehm HL, Watson MS, Williams MC, Biesecker LG. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genetics in Medicine. 2013; 15(7): 565-74.

Meet Our Team

The Center for Medical Ethics and Health Policy team is led by Director Amy L. McGuire, J.D., Ph.D.

View Faculty And Staff Listing

John Sulston, the projects namesake, was a champion of sharing scientific data to improve science and inform clinical decisions. Fittingly, he helped establish the 1996 Bermuda Principles with goals of rapid, electronic sharing of data generated by the Human Genome Project to benefit science and society. Today, sharing of genomic data has become more commonplace and yet still incredibly challenging to do.

Despite a growing norm of open science, concerns about proprietary rights remain a barrier to collecting and sharing data on a large scale for research and clinical use for all inherited cancer variants, or what could be called a cancer genomic variant commons. As more efforts to create cancer genomic variant commons that provide open access to data pooled from multiple sources are underway, such as the National Cancer Institute Genomic Data Commons, policies are evolving that could become a model for genomic data sharing more generally.

The overarching goal of the Sulston Project is to develop empirically-informed policy options to address the challenges of the nascent cancer genomic variant commons. We will engage relevant stakeholders to accomplish this work and inform policy in a way that balances proprietary and commercial interests with the generation of a public good -- information and knowledge about cancer-risk variants -- for public health benefit.

We aim to:

Describe data sharing structures and practices for inherited cancer-risk variants.
Identify the challenges of developing a sustainable commons for inherited cancer-risk variants.
Formulate policy options to address the most important challenges identified, and map policy options to institutions and actors who can act on them.
Translate findings and policy options by engaging with policy-makers and other actors.

Supported by: R01CA237118, National Cancer Institute, NIH, 2019 - 2023

Additional Project Information

Read more about our related work by visiting the webpage for two related studies: the PoliSeq project (McGuire R01 HG006460) examined the clinical integration of next generation sequencing technologies using a modified policy Delphi process, and Building the Medical Information Commons (McGuire R01 HG008918) examined issues confronted in fulfilling the aspirations of the 2011 NASEM report on Precision Medicine, which called for the creation of medical information commons.

Visit the for more information.

Publication

Robinson JO, Daoud A, Geary J, et al. Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi. J Law Biosci. 2023;10(2):lsad022. Published 2023 Jul 14. doi:10.1093/jlb/lsad022

Deverka P, Geary J, Mathews C, et al. Payer reimbursement practices and incentives for improving interpretation of germline genetic testing. J Law Biosci. 2023;10(2):lsad020. Published 2023 Jul 9. doi:10.1093/jlb/lsad020

Majumder MA, Blank ML, Geary J, Bollinger JM, Guerrini CJ, Robinson JO, Canfield I, Cook-Deegan R, McGuire AL. . Journal of Personalized Medicine. 2021 Jul 8;11(7):646.

Presentations

Fresh Air for Genetic Data Sharing. ELSIcon2022: Innovating for a Just and Equitable Future. Guerrini C, McGuire A, Robinson J, Blank M, Cook-Deegan R, Bollinger J, Geary J, Majumder M (2022).

Majumder MA, Gutierrez AM, Geary J, McGuire AL. “Equity considerations, challenges, and policy options for creating an effective knowledge commons for hereditary cancer risk.” American Society for Bioethics and Humanities Annual Conference. October 13-16, 2021. Panel presentation.

Supplement Project: A Case Study on Latinx Community Perspectives about Creating a Cancer Genomic Variant Commons

This qualitative case study is a Sulston supplement project that aims to explore the experiences of Hispanic/Latino communities in the U.S. with genetic testing for hereditary cancer risk. To do this, we are conducting 60 interviews across the U.S. with three stakeholder groups: genetics experts, patient advocates, and patients/members of the community. Through these stakeholder interviews, we will identify challenges and potential policy options related to improving access to genetic testing among Hispanic/Latino groups, with special attention to the heterogeneity of the US Hispanic/Latino population. This study includes a focus on policy translation, where we will communicate our empirical findings and policy implications to stakeholders, policymakers, and the scientific community. This project complements the goals of the Sulston Project by helping propose policy options for more effective inclusion of underserved groups in a cancer genomic variant commons.

Supported by: R01CA237118-S1, National Cancer Institute, NIH

Publication

Gutierrez AM, McGuire AL, Cook-Deegan R. “Disparities in access to genetic testing for hereditary cancer risk among Hispanic/Latino populations: Stakeholders’ views of barriers and potential solutions.” American Public Health Association Annual Meeting. October 23-27, 2021. Poster presentation.

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