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Author Details
Full Name
Cynthia A Prows
Affiliation
Cincinnati Children's Hospital Medical Center
ORCID
Career Start Year
1989
Papers
102
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37632220
Young adults' reasoning for involving a parent in a genomic decision-making research study.
J Genet Couns
2024
36715063
Implementation of CYP2D6-guided opioid therapy at Cincinnati Children's Hospital Medical Center.
Am J Health Syst Pharm
2023
37704356
Current Practices in Pharmacogenomics.
Pediatr Clin North Am
2023
37790445
Genetic Sex Validation for Sample Tracking in Clinical Testing.
Res Sq
2023
37883979
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Am J Hum Genet
2023
37343562
Studying the impact of translational genomic research: Lessons from eMERGE.
Am J Hum Genet
2023
37201682
Adolescent Decision-Making Involvement in the Receipt of Genomic Testing Results.
J Pediatr
2023
37162875
Engaging Adolescents and Young Adults in Decisions About Return of Genomic Research Results: a mixed-methods longitudinal clinical trial protocol.
Res Sq
2023
36751037
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature.
Am J Med Genet A
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
34695272
Experiences of adolescents and their parents after receiving adolescents' genomic screening results.
J Genet Couns
2022
35753502
A retrospective examination of adjunctive L-methylfolate in children and adolescents with unipolar depression.
J Affect Disord
2022
35595084
Multiancestral polygenic risk score for pediatric asthma.
J Allergy Clin Immunol
2022
36618804
Association of <i>CYP2D6</i> genotype predicted phenotypes with oxycodone requirements and side effects in children undergoing surgery.
Ann Transl Med
2022
36422086
Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.
J Pers Med
2022
36532300
Developing video education materials for the return of genomic test results to parents and adolescents.
PEC Innov
2022
35216901
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
2022
34906510
Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates.
Genet Med
2022
34670017
Influence of CYP2D6 metabolizer status on ondansetron efficacy in pediatric patients undergoing hematopoietic stem cell transplantation: A case series.
Clin Transl Sci
2022
34665896
Do research participants share genomic screening results with family members?
J Genet Couns
2022
33387367
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2D6, OPRM1, and COMT Genotypes and Select Opioid Therapy.
Clin Pharmacol Ther
2021
37920232
Facilitating Genetics Aware Clinical Decision Support: Putting the eMERGE Infrastructure into Practice.
ACI open
2021
36046768
Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.
Am J Med Genet A
2021
32349224
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.
J Pers Med
2020
36177089
Adapting Clinical Systems to Enable Adolescents' Genomic Choices.
ACI open
2020
31685375
Adolescents' and Parents' Genomic Testing Decisions: Associations With Age, Race, and Sex.
J Adolesc Health
2020
31654527
Decisional conflict among adolescents and parents making decisions about genomic sequencing results.
Clin Genet
2020
32669677
Participant choices for return of genomic results in the eMERGE Network.
Genet Med
2020
32413979
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.
J Pers Med
2020
30467830
The Case for Pharmacogenetics-Guided Prescribing of Codeine in Children.
Clin Pharmacol Ther
2019
31737042
Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network.
Front Genet
2019
30058217
Implementation of Pharmacogenetics at Cincinnati Children's Hospital Medical Center: Lessons Learned Over 14 Years of Personalizing Medicine.
Clin Pharmacol Ther
2019
31493347
Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic features.
Mol Genet Genomic Med
2019
31390496
Thyroid Function Screening in Children and Adolescents With Mood and Anxiety Disorders.
J Clin Psychiatry
2019
30837874
Influence of CYP2C19 Metabolizer Status on Escitalopram/Citalopram Tolerability and Response in Youth With Anxiety and Depressive Disorders.
Front Pharmacol
2019
31110330
Genomic education for the next generation of health-care providers.
Genet Med
2019
30427735
Racial Differences in Escitalopram/Citalopram-Related Weight Gain in Children and Adolescents: A Natural Language Processing-Based Electronic Medical Record Study.
J Child Adolesc Psychopharmacol
2019
30375152
Using human sequencing to guide craniofacial research.
Genesis
2019
30369597
Giving adolescents a voice: the types of genetic information adolescents choose to learn and why.
Genet Med
2019
29301385
Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.
J Pers Med
2018
29806518
Adolescent and Parental Attitudes About Return of Genomic Research Results: Focus Group Findings Regarding Decisional Preferences.
J Empir Res Hum Res Ethics
2018
29463693
Content analysis of requests for religious exemptions from a mandatory influenza vaccination program for healthcare personnel.
J Med Ethics
2018
27573590
Parental Perception of Self-Empowerment in Pediatric Pharmacogenetic Testing: The Reactions of Parents to the Communication of Actual and Hypothetical CYP2D6 Test Results.
Health Commun
2017
28502727
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.
J Mol Diagn
2017
29036432
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly.
Hum Mol Genet
2017
28745549
Prior opioid exposure influences parents' sharing of their children's CYP2D6 research results.
Pharmacogenomics
2017
28639489
Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience.
Pharmacogenomics
2017
28002639
Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2D6 genotype and use of ondansetron and tropisetron.
Clin Pharmacol Ther
2017
26857349
Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.
Clin Pharmacol Ther
2016
25521773
Opioid-related adverse effects in children undergoing surgery: unequal burden on younger girls with higher doses of opioids.
Pain Med
2015
1 - 50 of 102
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Johns Hopkins McKusick-Nathans Department of Genetic Medicine
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Collaborators
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Mayo Clinic
Co-authored papers
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Kaiser Permanente Washington
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Richard R Sharp
Biomedical Ethics, Mayo Clinic and Foundation
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Margaret Harr
Center for Applied Genomics, Children's Hospital of Philadelphia
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Hakon Hakonarson
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Josh F Peterson
Vanderbilt University Medical Center
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Michelle L McGowan
Biomedical Ethics Research Program, Mayo Clinic
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Georgia L Wiesner
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
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Christin Hoell
Northwestern University, Center for Genetic Medicine
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E Clayton
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Sharon Aufox
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Julia Wynn
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