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Author Details
Full Name
Tara J Schmidlen
Affiliation
Invitae Corporation
ORCID
Career Start Year
2010
Papers
31
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36243653
Implementing comprehensive pharmacogenomics in a community hospital-associated primary care setting.
J Am Pharm Assoc (2003)
2023
37020233
Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia.
BMC Health Serv Res
2023
37214500
Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study.
PEC Innov
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36556194
Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug-Gene, Drug-Drug-Gene, and Drug-Gene-Gene Interaction Risks in a Large Patient Population.
J Pers Med
2022
35616645
Use of a chatbot to increase uptake of cascade genetic testing.
J Genet Couns
2022
35783293
The Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives.
Front Genet
2022
33480803
Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hypercholesterolemia.
Circ Genom Precis Med
2021
33131927
Testing a best practices risk result format to communicate genetic risks.
Patient Educ Couns
2021
32340147
Pharmacogenomic (PGx) Counseling: Exploring Participant Questions about PGx Test Results.
J Pers Med
2020
32635876
PARC report: a perspective on the state of clinical pharmacogenomics testing.
Pharmacogenomics
2020
32601386
Clinical outcomes of a genomic screening program for actionable genetic conditions.
Genet Med
2020
31549758
Patient assessment of chatbots for the scalable delivery of genetic counseling.
J Genet Couns
2019
29460110
Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
J Genet Couns
2018
30046027
Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health.
J Pers Med
2018
30094286
Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR.
EGEMS (Wash DC)
2018
27322592
EMR documentation of physician-patient communication following genomic counseling for actionable complex disease and pharmacogenomic results.
Clin Genet
2017
28181117
CYP2D6 Genetic Variation and Beta-Blocker Maintenance Dose in Patients with Heart Failure.
Pharm Res
2017
28345121
Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.
J Genet Couns
2017
29263822
Precision Military Medicine: Conducting a multi-site clinical utility study of genomic and lifestyle risk factors in the United States Air Force.
NPJ Genom Med
2017
27921197
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.
J Genet Couns
2017
27527156
Challenges in Translating GWAS Results to Clinical Care.
Int J Mol Sci
2016
26306685
Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative.
J Genet Couns
2016
27121899
An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance.
Thromb Haemost
2016
25695399
Common genetic risk for melanoma encourages preventive behavior change.
J Pers Med
2015
26333835
Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration.
Am J Med Genet B Neuropsychiatr Genet
2015
24488620
Personalized genomic results: analysis of informational needs.
J Genet Couns
2014
24926413
Design and implementation of a randomized controlled trial of genomic counseling for patients with chronic disease.
J Pers Med
2014
24134832
The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system.
Genome Med
2013
21233721
Genetic risk estimation in the Coriell Personalized Medicine Collaborative.
Genet Med
2011
29776223
Coriell Personalized Medicine Collaborative<sup>®</sup>: a prospective study of the utility of personalized medicine.
Per Med
2010
1 - 31 of 31
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School of Public Health.
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Susan K Delaney
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Co-authored papers
2
Eden Haverfield
Invitae Corporation
Co-authored papers
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Adam H Buchanan
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Wolfgang Sad??e
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Elizabeth W Karlson
Brigham and Women's Hospital
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Janet L Williams
Genomic Medicine Institute
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Jodell E Linder
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1
Cynthia A Prows
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Christin Hoell
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