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Author Details

Maureen E Smith
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
2010
57
21
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37758692Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets.Nat Commun2023
37790445Genetic Sex Validation for Sample Tracking in Clinical Testing.Res Sq2023
37343562Studying the impact of translational genomic research: Lessons from eMERGE.Am J Hum Genet2023
37246632Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.Genet Med2023
37308598Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists.Eur J Hum Genet2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
34665896Do research participants share genomic screening results with family members?J Genet Couns2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
35339388Integrating clinical genetics in cardiology: Current practices and recommendations for education.Genet Med2022
35322684Practitioners' Confidence and Desires for Education in Cardiovascular and Sudden Cardiac Death Genetics.J Am Heart Assoc2022
34410195Communicating With Diverse Patients About Participating in a Biobank: A Randomized Multisite Study Comparing Electronic and Face-to-Face Informed Consent Processes.J Empir Res Hum Res Ethics2022
32945059Comprehension and personal value of negative non-diagnostic genetic panel testing.J Genet Couns2021
36046768Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.Am J Med Genet A2021
33926532Application of a framework to guide genetic testing communication across clinical indications.Genome Med2021
34945775Defining the Critical Components of Informed Consent for Genetic Testing.J Pers Med2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
33951936Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network.Circ Heart Fail2021
32349224Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.J Pers Med2020
32009526Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants.J Am Heart Assoc2020
32669677Participant choices for return of genomic results in the eMERGE Network.Genet Med2020
32413979Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.J Pers Med2020
32270628Impact of CYP2C9-Interacting Drugs on Warfarin Pharmacogenomics.Clin Transl Sci2020
30590688Enrichment sampling for a multi-site patient survey using electronic health records and census data.J Am Med Inform Assoc2019
29976988Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background.Genet Med2019
30778576An ancillary genomics system to support the return of pharmacogenomic results.J Am Med Inform Assoc2019
28656483Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results.J Community Genet2018
30240342Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.AJOB Empir Bioeth2018
30096823What People Want to Know About Their Genes: A Critical Review of the Literature on Large-Scale Genome Sequencing Studies.Healthcare (Basel)2018
30011878Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention Pairs.Healthcare (Basel)2018
29301385Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.J Pers Med2018
28639489Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience.Pharmacogenomics2017
28222112Genome-wide study of resistant hypertension identified from electronic health records.PLoS One2017
28190457Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.Am J Hum Genet2017
28502727Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.J Mol Diagn2017
26857349Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.Clin Pharmacol Ther2016
26583683A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.Genet Med2016
27881091Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.BMC Med Res Methodol2016
27359094Response to Patryn and Zagaja.Genet Med2016
26093003Factors Associated With Long-Term Weight Loss Following Bariatric Surgery Using 2 Methods for Repeated Measures Analysis.Am J Epidemiol2015
26365338Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.Am J Hum Genet2015
26337695rs4771122 Predicts Multiple Measures of Long-Term Weight Loss After Bariatric Surgery.Obes Surg2015
26255974A Validated Phenotyping Algorithm for Genetic Association Studies in Age-related Macular Degeneration.Sci Rep2015
24723935Return of results in the genomic medicine projects of the eMERGE network.Front Genet2014
25177340Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index.Front Genet2014
24960519Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems.Clin Pharmacol Ther2014
24717952Accuracy of phenotyping chronic rhinosinusitis in the electronic health record.Am J Rhinol Allergy2014
23743551The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.Genet Med2013
24159428Biobanking: The Melding of Research with Clinical Care.Curr Genet Med Rep2013
23965923Communication by mothers with breast cancer or melanoma with their children.Int J Environ Res Public Health2013
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Collaborators

Gail P Jarvik
University of Washington Medical Center
Co-authored papers 22
Ingrid A Holm
Harvard Medical School
Co-authored papers 20
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 17
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 16
Sharon Aufox
Northwestern University, Center for Genetic Medicine
Co-authored papers 16
Cynthia A Prows
Cincinnati Children's Hospital Medical Center
Co-authored papers 15
Marc S Williams
University of Washington Medical Center
Co-authored papers 15
Laura J Rasmussen-Torvik
Northwestern University, Center for Genetic Medicine
Co-authored papers 15
John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 15
Catherine A McCarty
University of Minnesota Medical School, 1035 University Drive duluth
Co-authored papers 15
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers 13
Kathleen A Leppig
Kaiser Permanente Washington
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Janet L Williams
Genomic Medicine Institute
Co-authored papers 12
Eric B Larson
University of Washington
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Melanie F Myers
Cincinnati Children's Hospital Medical Center
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Rex L Chisholm
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
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Wendy K Chung
Boston Children's Hospital, Harvard Medical School
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Josh F Peterson
Vanderbilt University Medical Center
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Margaret Harr
Center for Applied Genomics, Children's Hospital of Philadelphia
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Stephanie M Fullerton
University of Washington School of Medicine
Co-authored papers 10
Joshua C Denny
Vanderbilt University
Co-authored papers 10
Rongling Li
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 10
Christin Hoell
Northwestern University, Center for Genetic Medicine
Co-authored papers 10
Richard R Sharp
Biomedical Ethics, Mayo Clinic and Foundation
Co-authored papers 9
David R Crosslin
University of Washington Medical Center
Co-authored papers 9
Adam S Gordon
Northwestern University Feinberg School of Medicine.
Co-authored papers 9
Julia Wynn
Vagelos College of Physicians and Surgeons, Columbia University
Co-authored papers 9
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 9
Murray H Brilliant
Marshfield Clinic Research Institute
Co-authored papers 9
David S Carrell
Kaiser Permanente Washington Health Research Institute
Co-authored papers 8
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