| 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 | 418 | 2017 |
| 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 | 112 | 2019 |
| 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 | 83 | 2022 |
| 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 | 58 | 2020 |
| 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 | 41 | 2021 |
| 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 | 28 | 2021 |
| 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 | 25 | 2022 |
| 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 | 25 | 2020 |
| 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 | 20 | 2022 |
| 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 | 20 | 2020 |
| 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 | 18 | 2022 |
| 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 | 18 | 2021 |
| 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 | 18 | 2021 |
| 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 | 14 | 2022 |
| 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 | 13 | 2021 |
| 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 | 13 | 2020 |
| 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 | 8 | 2022 |
| 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 | 8 | 2021 |
| 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 | 7 | 2021 |
| Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project S Pereira, AM Gutierrez, JO Robinson, KD Christensen, CA Genetti, ... Genetics in Medicine 25 (3), 100002, 2023 | 6 | 2023 |
Heidi RussellProfessor, UTHealth Houston School of Public HealthVahvistettu sähköpostiosoite verkkotunnuksessa uth.tmc.edu
