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Author Details
Full Name
Hadley Stevens Smith
Affiliation
Center for Medical Ethics and Health Policy, Baylor College of Medicine
ORCID
Career Start Year
2017
Papers
36
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
38064200
The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care.
Clin Transl Sci
2024
36567057
Lessons learned while starting multi-institutional genetics research in diverse populations: A report from the Clinical Sequencing Evidence-Generating Research (CSER) consortium.
Contemp Clin Trials
2023
37563063
Pediatric Genomic Medicine: Value, Implementation, and Access.
Clin Ther
2023
37550140
Conversations With the Editors: Stewardship in Genomic Medicine-Insights From Health Care Payers at the Forefront of Clinical Innovation and Partnerships.
Clin Ther
2023
37470118
Parent-Reported Clinical Utility of Pediatric Genomic Sequencing.
Pediatrics
2023
37339288
The Other Side of the Self-Advocacy Coin: How For-Profit Companies Can Divert the Path to Justice in Rare Disease.
Am J Bioeth
2023
37468037
Clinically Indicated Genomic Sequencing of Children in Foster Care: Legal and Ethical Issues.
J Pediatr
2023
37238322
Framing the Family: A Qualitative Exploration of Factors That Shape Family-Level Experience of Pediatric Genomic Sequencing.
Children (Basel)
2023
36547467
Access to clinically indicated genetic tests for pediatric patients with Medicaid: Evidence from outpatient genetics clinics in Texas.
Genet Med
2023
36434257
Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research.
Eur J Hum Genet
2023
34416842
Sex Education on TikTok: A Content Analysis of Themes.
Health Promot Pract
2022
35353613
A Review of the MINDSPACE Framework for Nudging Health Promotion During Early Stages of the COVID-19 Pandemic.
Popul Health Manag
2022
35833928
Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods.
Genet Med
2022
35571041
Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study.
Front Genet
2022
35691983
Quality of life, illness perceptions, and parental lived experiences in TANGO2-related metabolic encephalopathy and arrhythmias.
Eur J Hum Genet
2022
35947388
Genomic Medicine's Critical Outcome Measure-Utility.
JAMA Netw Open
2022
36282588
Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study.
Circ Genom Precis Med
2022
35256804
A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States.
Nat Genet
2022
34906461
US private payers' perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER).
Genet Med
2022
34658003
Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development.
Patient
2022
33011736
Perceptions of best practices for return of results in an international survey of psychiatric genetics researchers.
Eur J Hum Genet
2021
33728981
Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications.
Per Med
2021
34888063
Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium.
J Clin Transl Sci
2021
34459727
How Should Economic Value Be Considered in Treatment Decisions for Individual Patients?
AMA J Ethics
2021
34424265
Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial.
JAMA Pediatr
2021
34687653
Conceptualization of utility in translational clinical genomics research.
Am J Hum Genet
2021
34363016
Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications.
Genet Med
2021
34362857
Appropriate Care for Adolescent Eating Disorders in Isolating and Disruptive Times.
J Cogn Psychother
2021
33473204
Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics.
Genet Med
2021
33481188
Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication.
J Community Genet
2021
32336750
Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions.
Genet Med
2020
33948230
Lessons learned about harmonizing survey measures for the CSER consortium.
J Clin Transl Sci
2020
31740737
Commentary on the development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE).
Genet Med
2020
33119106
Cost-effectiveness of Population-Wide Genomic Screening for Hereditary Breast and Ovarian Cancer in the United States.
JAMA Netw Open
2020
29760485
Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature.
Genet Med
2019
28973083
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
JAMA Pediatr
2017
1 - 36 of 36
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