Hadley Stevens Smith

TitlePostdoc Fellows and Associates
InstitutionBaylor College of Medicine
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    K99HG011491     (SMITH, HADLEY STEVENS)Dec 17, 2020 - Nov 30, 2022
    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. 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 May; 18(3):209-212. PMID: 33728981.
      Citations:    Fields:    
    2. 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 Jan 22. PMID: 33481188.
    3. 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 May; 23(5):950-955. PMID: 33473204.
      Citations:    Fields:    
    4. 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 Feb; 29(2):231-240. PMID: 33011736.
      Citations:    Fields:    
    5. 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: 1     Fields:    Translation:Humans
    6. 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.
    7. 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:    
    8. 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: 14     Fields:    Translation:Humans
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