Hadley Stevens Smith

TitlePostdoc Fellows and Associates
InstitutionBaylor College of Medicine
DepartmentPostDoc
Address
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    K99HG011491     (SMITH, HADLEY STEVENS)Dec 17, 2020 - Nov 30, 2022
    NIH
    An ELSI-Integrated Evaluation of the Family-Level Utility of Pediatric Genomic Sequencing
    Role: Principal Investigator

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Murali CN, Lalani SR, Azamian MS, Miyake CY, Smith HS. Quality of life, illness perceptions, and parental lived experiences in TANGO2-related metabolic encephalopathy and arrhythmias. Eur J Hum Genet. 2022 Jun 13. PMID: 35691983.
      Citations:    Fields:    
    2. Armstrong B, Christensen KD, Genetti CA, Parad RB, Robinson JO, Blout Zawatsky CL, Zettler B, Beggs AH, Holm IA, Green RC, McGuire AL, Smith HS, Pereira S. Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study. Front Genet. 2022; 13:867371. PMID: 35571041.
      Citations:    
    3. Smith HS, Blumenthal-Barby JS, Chatterjee R, Hindera O, Huang A, Kothari R, Vlaev I. A Review of the MINDSPACE Framework for Nudging Health Promotion During Early Stages of the COVID-19 Pandemic. Popul Health Manag. 2022 Mar 28. PMID: 35353613.
      Citations:    Fields:    
    4. Halley MC, Smith HS, Ashley EA, Goldenberg AJ, Tabor HK. A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States. Nat Genet. 2022 03; 54(3):219-222. PMID: 35256804.
      Citations:    Fields:    Translation:Humans
    5. Phillips KA, Trosman JR, Douglas MP, Gelb BD, Ferket BS, Hindorff LA, Slavotinek AM, Berg JS, Russell HV, Devine B, Greve V, Smith HS. 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 01; 24(1):238-244. PMID: 34906461.
      Citations:    Fields:    Translation:HumansCells
    6. Pereira S, Smith HS, Frankel LA, Christensen KD, Islam R, Robinson JO, Genetti CA, Blout Zawatsky CL, Zettler B, Parad RB, Waisbren SE, Beggs AH, Green RC, Holm IA, McGuire AL. Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial. JAMA Pediatr. 2021 11 01; 175(11):1132-1141. PMID: 34424265.
      Citations: 2     Fields:    Translation:HumansPHPublic Health
    7. Smith HS, Brothers KB, Knight SJ, Ackerman SL, Rini C, Veenstra DL, McGuire AL, Wilfond BS, Malek J. Conceptualization of utility in translational clinical genomics research. Am J Hum Genet. 2021 11 04; 108(11):2027-2036. PMID: 34687653.
      Citations:    Fields:    Translation:Humans
    8. Smith HS, Morain SR, Robinson JO, Canfield I, Malek J, Rubanovich CK, Bloss CS, Ackerman SL, Biesecker B, Brothers KB, Goytia CN, Horowitz CR, Knight SJ, Koenig B, Kraft SA, Outram S, Rini C, Shipman KJ, Waltz M, Wilfond B, McGuire AL. Perceived Utility of Genomic Sequencing: Qualitative Analysis and Synthesis of a Conceptual Model to Inform Patient-Centered Instrument Development. Patient. 2022 May; 15(3):317-328. PMID: 34658003.
      Citations:    Fields:    Translation:Humans
    9. Gutierrez AM, Robinson JO, Outram SM, Smith HS, Kraft SA, Donohue KE, Biesecker BB, Brothers KB, Chen F, Hailu B, Hindorff LA, Hoban H, Hsu RL, Knight SJ, Koenig BA, Lewis KL, Lich KH, O'Daniel JM, Okuyama S, Tomlinson GE, Waltz M, Wilfond BS, Ackerman SL, Majumder MA. Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium. J Clin Transl Sci. 2021; 5(1):e193. PMID: 34888063.
      Citations: 1     
    10. Fowler LR, Schoen L, Smith HS, Morain SR. Sex Education on TikTok: A Content Analysis of Themes. Health Promot Pract. 2021 Aug 20; 15248399211031536. PMID: 34416842.
      Citations: 3     Fields:    
    11. Murdock DR, Venner E, Muzny DM, Metcalf GA, Murugan M, Hadley TD, Chander V, de Vries PS, Jia X, Hussain A, Agha AM, Sabo A, Li S, Meng Q, Hu J, Tian X, Cohen M, Yi V, Kovar CL, Gingras MC, Korchina V, Howard C, Riconda DL, Pereira S, Smith HS, Huda ZA, Buentello A, Marino PR, Leiber L, Balasubramanyam A, Amos CI, Civitello AB, Chelu MG, Maag R, McGuire AL, Boerwinkle E, Wehrens XHT, Ballantyne CM, Gibbs RA. Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications. Genet Med. 2021 12; 23(12):2404-2414. PMID: 34363016.
      Citations: 1     Fields:    Translation:Humans
    12. Smith HS, Morain SR. Appropriate Care for Adolescent Eating Disorders in Isolating and Disruptive Times. J Cogn Psychother. 2021 08 01; 35(3):153-155. PMID: 34362857.
      Citations:    Fields:    Translation:Humans
    13. Smith HS. How Should Economic Value Be Considered in Treatment Decisions for Individual Patients? AMA J Ethics. 2021 08 01; 23(8):E607-612. PMID: 34459727.
      Citations:    Fields:    Translation:Humans
    14. Smith HS, McGuire AL, Wittenberg E, Lavelle TA. Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications. Per Med. 2021 05; 18(3):209-212. PMID: 33728981.
      Citations: 1     Fields:    Translation:Humans
    15. Makhnoon S, Smith HS, Bednar EM, Bhatt A, Turner L, Arun B, Volk RJ, Peterson SK. Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication. J Community Genet. 2021 Jul; 12(3):439-447. PMID: 33481188.
      Citations: 2     
    16. Smith HS, Franciskovich R, Lewis AM, Gerard A, Littlejohn RO, Nugent K, Rodriguez J, Streff H. Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics. Genet Med. 2021 05; 23(5):950-955. PMID: 33473204.
      Citations: 2     Fields:    Translation:Humans
    17. Lázaro-Muñoz G, Torgerson L, Smith HS, Pereira S. Perceptions of best practices for return of results in an international survey of psychiatric genetics researchers. Eur J Hum Genet. 2021 02; 29(2):231-240. PMID: 33011736.
      Citations: 2     Fields:    Translation:Humans
    18. Smith HS, Swint JM, Lalani SR, de Oliveira Otto MC, Yamal JM, Russell HV, Lee BH. Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions. Genet Med. 2020 08; 22(8):1303-1310. PMID: 32336750.
      Citations: 4     Fields:    Translation:Humans
    19. Goddard KAB, Angelo FAN, Ackerman SL, Berg JS, Biesecker BB, Danila MI, East KM, Hindorff LA, Horowitz CR, Hunter JE, Joseph G, Knight SJ, McGuire A, Muessig KR, Ou J, Outram S, Rahn EJ, Ramos MA, Rini C, Robinson JO, Smith HS, Waltz M, Lee SS. Lessons learned about harmonizing survey measures for the CSER consortium. J Clin Transl Sci. 2020 Apr 24; 4(6):537-546. PMID: 33948230.
      Citations: 4     
    20. Rubanovich CK, Smith HS, Bloss CS. Commentary on the development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE). Genet Med. 2020 03; 22(3):665-666. PMID: 31740737.
      Citations:    Fields:    
    21. Smith HS, Swint JM, Lalani SR, Yamal JM, de Oliveira Otto MC, Castellanos S, Taylor A, Lee BH, Russell HV. Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature. Genet Med. 2019 01; 21(1):3-16. PMID: 29760485.
      Citations: 31     Fields:    Translation:Humans
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