Jennifer B. McCormick

发表

Enrichment sampling for a multi-site patient survey using electronic health records and census data

Sarah C. Stallings, Jonathan S. Schildcrout, Gail P. Jarvik, 2019, J. Am. Medical Informatics Assoc..

Noralane Morey Lindor, Jennifer B. McCormick, Kiley J. Johnson, 2015 .

Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials

Adam A. Nishimura, Jennifer B. McCormick, Jennifer B McCormick, 2013, BMC Medical Ethics.

Beyond Sputnik: U.S. Science Policy in the Twenty-First Century

Homer A. Neal, Jennifer B. McCormick, Tobin L. Smith, 2008 .

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.

Jonathan S. Schildcrout, Stephanie M. Fullerton, Gail P. Jarvik, 2017, American journal of human genetics.

Neurotalk: improving the communication of neuroscience research

Judy Illes, Erika Check Hayden, Sandra Blakeslee, 2010, Nature Reviews Neuroscience.

Stakeholder engagement: a key component of integrating genomic information into electronic health records

Erica A. Bowton, Andrea Hartzler, Kadija Ferryman, 2013, Genetics in Medicine.

The Genomic Novel and Priority Mapping Tool: Using Empathic Design to Develop Innovative Patient-Centered Decision-Making Tools for the Genomic Testing Experience

Noralane Morey Lindor, Jennifer B. McCormick, Kiley J. Johnson, 2016 .

Public Perceptions of Disease Severity but Not Actionability Correlate with Interest in Receiving Genomic Results: Nonalignment with Current Trends in Practice

Jennifer B. McCormick, Pamela S. Sinicrope, N. Lindor, 2015, Public Health Genomics.

Preserving personal autonomy in a genomic testing era

Eric W. Klee, Gianrico Farrugia, Matthew J. Ferber, 2013, Genetics in Medicine.

Neighborhood socioeconomic status and stroke mortality: Disentangling individual and area effects

Jennifer B. McCormick, M. Mittal, 2013, Neurology.

Translating Gene Transfer: A Stalled Effort

Jennifer B. McCormick, A. Windebank, A. Greenberg, 2011, Clinical and translational science.

How Patients View Probiotics: Findings From a Multicenter Study of Patients With Inflammatory Bowel Disease and Irritable Bowel Syndrome

Jennifer B. McCormick, P. Marshall, G. Geller, 2012, Journal of clinical gastroenterology.

Are patients willing to incur out of pocket costs for pharmacogenomic testing?

Jennifer B. McCormick, P. Caraballo, J. Olson, 2016, The Pharmacogenomics Journal.

Patients’ views on variants of uncertain significance across indications

Jennifer B. McCormick, A. A. Abu Dabrh, Kristin E Clift, 2019, Journal of Community Genetics.

Addiction: Current Criticism of the Brain Disease Paradigm

Jennifer B. McCormick, B. Koenig, Brad Partridge, 2013, AJOB neuroscience.

When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority.

Melissa A. Basford, John A. Lynch, Terrie E. Kitchner, 2016, The Journal of pediatrics.

Development and testing of a tool to assess patient preferences for phase I clinical trial participation

Jennifer B. McCormick, F. Khuri, T. Owonikoko, 2015, Psycho-oncology.

The Stem-Cell Century: A New Epoch and Fresh Challenge

Jennifer B. McCormick, C. Scott, 2009, Perspectives in biology and medicine.

Patients' views on incidental findings from clinical exome sequencing

Jennifer B. McCormick, R. Sharp, A. Kumbamu, 2015, Applied & translational genomics.

Was it worth it? Patients’ perspectives on the perceived value of genomic-based individualized medicine

Jennifer B. McCormick, Colin M. E. Halverson, Kristin E. Clift, 2016, Journal of Community Genetics.

Practical guidance on informed consent for pediatric participants in a biorepository.

John A. Lynch, John J. Connolly, Jennifer B. McCormick, 2014, Mayo Clinic proceedings.

Integrating Pharmacogenomics into Clinical Practice: Promise vs Reality.

Janet E Olson, Pedro J Caraballo, Suzette J Bielinski, 2016, The American journal of medicine.

“Why did I get that part of you?” Understanding addiction genetics through family history

Jennifer B. McCormick, B. Koenig, Jenny E. Ostergren, 2018, Public understanding of science.

“I don’t have to know why it snows, I just have to shovel it!”: Addiction recovery, genetic frameworks, and biological citizenship

Jennifer B. McCormick, B. Koenig, Jenny E. Ostergren, 2017, BioSocieties.

Unwarranted Optimism in Media Portrayals of Genetic Research on Addiction Overshadows Critical Ethical and Social Concerns

Jennifer B. McCormick, B. Koenig, Jenny E. Ostergren, 2015, Journal of health communication.

Silent Tyrosinemia Type I Without Elevated Tyrosine or Succinylacetone Associated with Liver Cirrhosis and Hepatocellular Carcinoma

Jennifer B. McCormick, S. Ekker, N. Giama, 2016, Human mutation.

The Media and Behavioral Genetics

Jennifer B. McCormick, B. Koenig, Jenny E. Ostergren, 2015, Science, technology & human values.

Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocol.

Christopher G Chute, Eric D Wieben, Jyotishman Pathak, 2014, Mayo Clinic proceedings.

Experiences of patients with chronic gastrointestinal conditions: in their own words

Jennifer B. McCormick, Katherine M. James, G. Geller, 2012, Health and Quality of Life Outcomes.

Implementing individualized medicine into the medical practice

Eric D Wieben, Gianrico Farrugia, Cloann Schultz, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

At a Moment’s Notice: Community Advisory Board Perspectives on Biobank Communication to Supplement Broad Consent

Jennifer B. McCormick, R. Sharp, K. Meagher, 2020, Public Health Genomics.

Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials

Adam A. Nishimura, Jennifer B. McCormick, P. Erwin, 2013, BMC medical ethics.

Assessing the stability of biobank donor preferences regarding sample use: evidence supporting the value of dynamic consent

Jennifer B. McCormick, J. Olson, R. Sharp, 2020, European Journal of Human Genetics.

Letter by Mittal and McCormick regarding article, "self-report of stroke, transient ischemic attack, or stroke symptoms and risk of future stroke in the REasons for Geographic and Racial Differences in Stroke (REGARDS) study".

Jennifer B. McCormick, M. Mittal, 2013, Stroke.

Molecular Modeling and Functional Analysis of Exome Sequencing–Derived Variants of Unknown Significance Identify a Novel, Constitutively Active FGFR2 Mutant in Cholangiocarcinoma

Gavin R. Oliver, Jennifer B. McCormick, Tammy M. McAllister, 2019 .

Experience with precision genomics and tumor board, indicates frequent target identification, but barriers to delivery

Gavin R. Oliver, Jennifer B. McCormick, J. Kocher, 2017, OncoTarget.

A patient-centered approach to the development and pilot of a warfarin pharmacogenomics patient education tool for health professionals

Jennifer B. McCormick, I. Kullo, C. Formea, 2015, Currents in pharmacy teaching & learning.

Was it worth it? Patients’ perspectives on the perceived value of genomic-based individualized medicine

Jennifer B. McCormick, Colin M. E. Halverson, Kristin E. Clift, 2016, Journal of Community Genetics.

Challenges in Translational Research: The Views of Addiction Scientists

Jennifer B. McCormick, B. Koenig, Jenny E. Ostergren, 2014, PloS one.

Bridging the gap: ethical considerations of providing psychological assessment results in research studies

Jennifer B. McCormick, R. Sharp, D. O. Warner, 2020 .

Whole-Exome Sequencing of 10 Scientists: Evaluation of the Process and Outcomes.

Jennifer B. McCormick, Kiley J. Johnson, Kimberly A. Schahl, 2015, Mayo Clinic proceedings.

Genomic Data in the Electronic Medical Record

Jennifer B. McCormick, Jennifer B McCormick, K. Maschke, 2014, Journal of empirical research on human research ethics : JERHRE.

Genomic medicine and incidental findings: balancing actionability and patient autonomy.

Jennifer B. McCormick, Kiley J. Johnson, Kimberly A. Schahl, 2014, Mayo Clinic proceedings.

Prudentia Populo: Involving the Community in Biobank Governance

Jennifer B. McCormick, R. Sharp, M. Allyse, 2015, The American journal of bioethics : AJOB.

Community-Engaged Research Ethics Review: Exploring Flexibility in Federal Regulations.

Jennifer B. McCormick, R. Sharp, E. Anderson, 2016, IRB.

Managing the Unimaginable: Biobank Participant Views on Reconsent for Whole Genome Sequencing of Stored Biospecimens.

Jennifer B. McCormick, J. Olson, R. Sharp, 2019, Biopreservation and biobanking.

Translating Gene Transfer: A Stalled Effort

Jennifer B. McCormick, A. Windebank, A. Greenberg, 2011, Clinical and translational science.

How Patients View Probiotics: Findings From a Multicenter Study of Patients With Inflammatory Bowel Disease and Irritable Bowel Syndrome

Jennifer B. McCormick, P. Marshall, G. Geller, 2012, Journal of clinical gastroenterology.

Parents’ attitudes toward consent and data sharing in biobanks: A multisite experimental survey

Jennifer B. McCormick, S. Fullerton, E. Clayton, 2018, AJOB empirical bioethics.

Integrating Pharmacogenomics into Clinical Practice: Promise vs Reality.

Jennifer B. McCormick, Carolyn R Rohrer Vitek, P. Caraballo, 2016, The American journal of medicine.

Genomic medicine and incidental findings: balancing actionability and patient autonomy.

Jennifer B. McCormick, Kiley J. Johnson, Kimberly A. Schahl, 2014, Mayo Clinic proceedings.

‘Someone should oversee it’: patient perspectives on the ethical issues arising with the regulation of probiotics

Jennifer B. McCormick, P. Marshall, G. Geller, 2015, Health expectations : an international journal of public participation in health care and health policy.

Conducting a large, multi-site survey about patients’ views on broad consent: challenges and solutions

Jonathan S. Schildcrout, Melissa A. Basford, Stephanie M. Fullerton, 2016, BMC Medical Research Methodology.

Patients’ views on variants of uncertain significance across indications

Jennifer B. McCormick, A. A. Abu Dabrh, Colin M. E. Halverson, 2019, Journal of Community Genetics.

Molecular Modeling and Functional Analysis of Exome Sequencing–Derived Variants of Unknown Significance Identify a Novel, Constitutively Active FGFR2 Mutant in Cholangiocarcinoma

Gavin R. Oliver, Jennifer B. McCormick, Tammy M. McAllister, 2017, JCO precision oncology.