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Hadley Stevens Smith
Hadley Stevens Smith
Harvard Pilgrim Health Care Institute
Verified email at harvardpilgrim.org - Homepage
Title
Cited by
Cited by
Year
Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management
L Meng, M Pammi, A Saronwala, P Magoulas, AR Ghazi, F Vetrini, ...
JAMA pediatrics 171 (12), e173438-e173438, 2017
4142017
Clinical application of genome and exome sequencing as a diagnostic tool for pediatric patients: a scoping review of the literature
HS Smith, JM Swint, SR Lalani, JM Yamal, MC de Oliveira Otto, ...
Genetics in Medicine 21 (1), 3-16, 2019
1122019
Sex education on TikTok: a content analysis of themes
LR Fowler, L Schön, HS Smith, SR Morain
Health promotion practice 23 (5), 739-742, 2022
772022
Cost-effectiveness of population-wide genomic screening for hereditary breast and ovarian cancer in the United States
GF Guzauskas, S Garbett, Z Zhou, SJ Spencer, HS Smith, J Hao, ...
JAMA network open 3 (10), e2022874-e2022874, 2020
562020
Psychosocial effect of newborn genomic sequencing on families in the BabySeq Project: a randomized clinical trial
S Pereira, HS Smith, LA Frankel, KD Christensen, R Islam, JO Robinson, ...
JAMA pediatrics 175 (11), 1132-1141, 2021
412021
Examining access to care in clinical genomic research and medicine: experiences from the CSER Consortium
AM Gutierrez, JO Robinson, SM Outram, HS Smith, SA Kraft, KE Donohue, ...
Journal of clinical and translational science 5 (1), e193, 2021
272021
Perceived utility of genomic sequencing: qualitative analysis and synthesis of a conceptual model to inform patient-centered instrument development
HS Smith, SR Morain, JO Robinson, I Canfield, J Malek, CK Rubanovich, ...
The Patient-Patient-Centered Outcomes Research, 1-12, 2022
252022
Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions
HS Smith, JM Swint, SR Lalani, MC de Oliveira Otto, JM Yamal, ...
Genetics in Medicine 22 (8), 1303-1310, 2020
242020
Parental attitudes toward standard newborn screening and newborn genomic sequencing: findings from the BabySeq study
B Armstrong, KD Christensen, CA Genetti, RB Parad, JO Robinson, ...
Frontiers in Genetics 13, 867371, 2022
202022
Lessons learned about harmonizing survey measures for the CSER consortium
KAB Goddard, FAN Angelo, SL Ackerman, JS Berg, BB Biesecker, ...
Journal of Clinical and Translational Science 4 (6), 537-546, 2020
202020
Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics
HS Smith, R Franciskovich, AM Lewis, A Gerard, RO Littlejohn, K Nugent, ...
Genetics in Medicine 23 (5), 950-955, 2021
172021
Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications
DR Murdock, E Venner, DM Muzny, GA Metcalf, M Murugan, TD Hadley, ...
Genetics in Medicine 23 (12), 2404-2414, 2021
162021
A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States
MC Halley, HS Smith, EA Ashley, AJ Goldenberg, HK Tabor
Nature genetics 54 (3), 219-222, 2022
152022
A review of the MINDSPACE framework for nudging health promotion during early stages of the COVID-19 Pandemic
HS Smith, JS Blumenthal-Barby, R Chatterjee, O Hindera, A Huang, ...
Population health management 25 (4), 487-500, 2022
142022
Conceptualization of utility in translational clinical genomics research
HS Smith, KB Brothers, SJ Knight, SL Ackerman, C Rini, DL Veenstra, ...
The American Journal of Human Genetics 108 (11), 2027-2036, 2021
132021
Using the Delphi method to identify clinicians’ perceived importance of pediatric exome sequencing results
H Stevens Smith, HV Russell, BH Lee, SR Morain, ...
Genetics in Medicine 22 (1), 69-76, 2020
102020
Using the Delphi method to identify clinicians’ perceived importance of pediatric exome sequencing results
HS Smith, HV Russell, BH Lee, SR Morain
Genetics in Medicine 22 (1), 69-76, 2020
92020
Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications
HS Smith, AL McGuire, E Wittenberg, TA Lavelle
Personalized Medicine 18 (3), 209-212, 2021
82021
US private payers’ perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium …
KA Phillips, JR Trosman, MP Douglas, BD Gelb, BS Ferket, LA Hindorff, ...
Genetics in Medicine 24 (1), 238-244, 2022
72022
Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication
S Makhnoon, HS Smith, EM Bednar, A Bhatt, L Turner, B Arun, RJ Volk, ...
Journal of Community Genetics 12, 439-447, 2021
72021
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