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Author Details
Full Name
Amy A Lemke
Affiliation
Norton Children's Research Institute, University of Louisville School of Medicine
ORCID
Career Start Year
1992
Papers
32
H Index
18
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36807341
Perceived benefits and barriers to implementing precision preventive care: Results of a national physician survey.
Eur J Hum Genet
2023
37511639
Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit.
J Pers Med
2023
36748708
Primary care physician use of patient race and polygenic risk scores in medical decision-making.
Genet Med
2023
36055208
Addressing underrepresentation in genomics research through community engagement.
Am J Hum Genet
2022
35803232
Digital health-enabled genomics: Opportunities and challenges.
Am J Hum Genet
2022
35545013
"A Gift to My Family for Their Future": Attitudes about Genetic Research Participation.
Public Health Genomics
2022
36459976
Addressing the challenges of polygenic scores in human genetic research.
Am J Hum Genet
2022
36039118
Assessing Vietnamese American patient perspectives on population genetic testing in primary care: A community-engaged approach.
HGG Adv
2022
34312282
Implementing Primary Care Mediated Population Genetic Screening Within an Integrated Health System.
J Am Board Fam Med
2021
33596141
Patient-Reported Outcomes and Experiences with Population Genetic Testing Offered Through a Primary Care Network.
Genet Test Mol Biomarkers
2021
33066060
Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment.
J Pers Med
2020
32020508
Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment.
J Community Genet
2020
29469671
Patient perspectives following pharmacogenomics results disclosure in an integrated health system.
Pharmacogenomics
2018
28672074
Collaborative Counseling Considerations for Pharmacogenomic Tests.
Pharmacotherapy
2017
29754567
Primary care physician experiences with integrated pharmacogenomic testing in a community health system.
Per Med
2017
25764215
Stakeholder engagement in policy development: challenges and opportunities for human genomics.
Genet Med
2015
23163796
Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study.
Clin Genet
2013
23239553
Maternal perspectives on the return of genetic results: context matters.
Am J Med Genet A
2013
22241102
Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis.
Genet Med
2012
22438108
Biobank participation and returning research results: perspectives from a deliberative engagement in South Side Chicago.
Am J Med Genet A
2012
21487211
Attitudes toward genetic research review: results from a survey of human genetics researchers.
Public Health Genomics
2011
21736136
Broad data sharing in genetic research: views of institutional review board professionals.
IRB
2011
20235866
Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protection.
J Empir Res Hum Res Ethics
2010
22962560
Community engagement in biobanking: Experiences from the eMERGE Network.
Genom Soc Policy
2010
20733502
Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium.
Genet Med
2010
20805700
Public and biobank participant attitudes toward genetic research participation and data sharing.
Public Health Genomics
2010
19752737
Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population.
Genet Med
2009
12433008
A brief assessment of concerns associated with genetic testing for cancer: the Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire.
Health Psychol
2002
26141097
Preconception Genetic Counseling: Three Years of Experience at a Community-Based Health Center.
J Genet Couns
1998
7505422
Delta F508 genotype does not predict disease severity in an ethnically diverse cystic fibrosis population.
Pediatrics
1994
1281385
Ethnic heterogeneity and cystic fibrosis transmembrane regulator (CFTR) mutation frequencies in Chicago-area CF families.
Am J Hum Genet
1992
24242075
Reproductive issues in adults with cystic fibrosis: Implications for genetic counseling.
J Genet Couns
1992
1 - 32 of 32
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