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Author Details
Full Name
Lori A Orlando
Affiliation
Duke University School of Medicine
ORCID
Career Start Year
2004
Papers
80
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36307642
A Cluster Randomized Trial of a Family Health History Platform to Identify and Manage Patients at Increased Risk for Colorectal Cancer.
J Gen Intern Med
2023
36983592
Expanding Family Health History to Include Family Medication History.
J Pers Med
2023
37246632
Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.
Genet Med
2023
36856778
Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?
Fam Pract
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36808791
Critical components of genomic medicine practice for non-genetics healthcare professionals: Genetic counselors' perspectives and implications for medical education.
J Genet Couns
2023
36081750
Comparative study of different SES neighborhood clinics for health literacy and internet access.
Digit Health
2022
35660539
Design and rationale of GUARDD-US: A pragmatic, randomized trial of genetic testing for APOL1 and pharmacogenomic predictors of antihypertensive efficacy in patients with hypertension.
Contemp Clin Trials
2022
36474257
Implementation-effectiveness trial of systematic family health history based risk assessment and impact on clinical disease prevention and surveillance activities.
BMC Health Serv Res
2022
33413596
Family history assessment significantly enhances delivery of precision medicine in the genomics era.
Genome Med
2021
33743786
Clinical implementation of an oncology-specific family health history risk assessment tool.
Hered Cancer Clin Pract
2021
34683187
Experience and Perceptions of a Family Health History Risk Assessment Tool among Multi-Ethnic Asian Breast Cancer Patients.
J Pers Med
2021
34071920
Multi-Institutional Implementation of Clinical Decision Support for <i>APOL1, NAT2,</i> and <i>YEATS4</i> Genotyping in Antihypertensive Management.
J Pers Med
2021
33972721
Genomic medicine implementation protocols in the PhenX Toolkit: tools for standardized data collection.
Genet Med
2021
34357114
Strategies to Integrate Genomic Medicine into Clinical Care: Evidence from the IGNITE Network.
J Pers Med
2021
34225778
Correction to: Family history assessment significantly enhances delivery of precision medicine in the genomics era.
Genome Med
2021
33288881
Correction: Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.
Genet Med
2021
32320338
The enduring importance of family health history in the era of genomic medicine and risk assessment.
Per Med
2020
31667742
Results and Lessons of a Pilot Study of Cascade Screening for Familial Hypercholesterolemia in US Primary Care Practices.
J Gen Intern Med
2020
33142667
Variant Interpretation in Current Pharmacogenetic Testing.
J Pers Med
2020
33160339
At the intersection of precision medicine and population health: an implementation-effectiveness study of family health history based systematic risk assessment in primary care.
BMC Health Serv Res
2020
33330735
Surgeon Applications of Patient Preferences in Treatment Decision Making for First-Time Anterior Shoulder Dislocation.
Orthop J Sports Med
2020
32719393
Correction: Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.
Genet Med
2020
32719392
Correction: Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working Group.
Genet Med
2020
32181122
Evaluation of family health history collection methods impact on data and risk assessment outcomes.
Prev Med Rep
2020
30467402
Qualitative study of system-level factors related to genomic implementation.
Genet Med
2019
31652289
Awareness of family health history in a predominantly young adult population.
PLoS One
2019
30158693
Correction: Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.
Genet Med
2019
29997387
Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.
Genet Med
2019
29875427
Implementation, adoption, and utility of family health history risk assessment in diverse care settings: evaluating implementation processes and impact with an implementation framework.
Genet Med
2019
31590688
An electronic family health history tool to identify and manage patients at increased risk for colorectal cancer: protocol for a randomized controlled trial.
Trials
2019
31331251
What will it take to implement genomics in practice? Lessons from the IGNITE Network.
Per Med
2019
31395443
Building evidence and measuring clinical outcomes for genomic medicine.
Lancet
2019
31395442
Family health history: underused for actionable risk assessment.
Lancet
2019
30895746
IGNITE network: Response of patients to genomic medicine interventions.
Mol Genet Genomic Med
2019
30866001
Effect of Sociodemographic Factors on Uptake of a Patient-Facing Information Technology Family Health History Risk Assessment Platform.
Appl Clin Inform
2019
30834817
Efficacy of a Preference-Based Decision Tool on Treatment Decisions for a First-Time Anterior Shoulder Dislocation: A Randomized Controlled Trial of At-Risk Patients.
Med Decis Making
2019
30997171
Use of clinical algorithms and rapid influenza testing to manage influenza-like illness: a cost-effectiveness analysis in Sri Lanka.
BMJ Glob Health
2019
31104772
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.
Am J Hum Genet
2019
28914267
Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working Group.
Genet Med
2018
27296809
Impact of Genetic Testing and Family Health History Based Risk Counseling on Behavior Change and Cognitive Precursors for Type 2 Diabetes.
J Genet Couns
2017
28406488
Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research.
Genet Med
2017
28377932
Understanding Preferences for Treatment After Hypothetical First-Time Anterior Shoulder Dislocation: Surveying an Online Panel Utilizing a Novel Shared Decision-Making Tool.
Orthop J Sports Med
2017
28532511
Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
BMC Med Genomics
2017
26729011
The IGNITE network: a model for genomic medicine implementation and research.
BMC Med Genomics
2016
29767594
Family health history: an essential starting point for personalized risk assessment and disease prevention.
Per Med
2016
26938783
Clinical utility of a Web-enabled risk-assessment and clinical decision support program.
Genet Med
2016
25120038
Use of a patient-entered family health history tool with decision support in primary care: impact of identification of increased risk patients on genetic counseling attendance.
J Genet Couns
2015
26597091
Protocol for the "Implementation, adoption, and utility of family history in diverse care settings" study.
Implement Sci
2015
26268266
Implementation of health risk assessments with family health history: barriers and benefits.
Postgrad Med J
2015
1 - 50 of 80
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Co-authored papers
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Institute for Health Equity Research, Icahn School of Medicine at Mount Sinai
Co-authored papers
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University of Wisconsin
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Toni I Pollin
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David Dimmock
Rady Children's Institute for Genomic Medicine
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Josh F Peterson
Vanderbilt University Medical Center
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Stephen E Kimmel
University of Florida
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Yue Guan
The Third Affiliated Hospital of Dalian Medical University
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