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Megan Roy-Puckelwartz

TitlePostdoctoral Scholar
InstitutionUniversity of Chicago
DepartmentMedicine
AddressChicago IL 60637
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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. Roy-Puckelwartz MJ. Pathogenic genes associated with sudden unexpected death in pediatrics. J Pediatr. 2022 10; 249:117-120. PMID: 36216474.
      Citations:    Fields:    Translation:Humans
    2. Tomaselli GF, Roy-Puckelwartz MJ. Early-Onset Atrial Fibrillation and Heritable Heart Disease-To Test or Not to Test? JAMA Cardiol. 2021 12 01; 6(12):1359-1361. PMID: 34495307.
      Citations: 2     Fields:    Translation:Humans
    3. Stanaway IB, Hall TO, Rosenthal EA, Palmer M, Naranbhai V, Knevel R, Namjou-Khales B, Carroll RJ, Kiryluk K, Gordon AS, Linder J, Howell KM, Mapes BM, Lin FTJ, Joo YY, Hayes MG, Gharavi AG, Pendergrass SA, Ritchie MD, de Andrade M, Croteau-Chonka DC, Raychaudhuri S, Weiss ST, Lebo M, Amr SS, Carrell D, Larson EB, Chute CG, Rasmussen-Torvik LJ, Roy-Puckelwartz MJ, Sleiman P, Hakonarson H, Li R, Karlson EW, Peterson JF, Kullo IJ, Chisholm R, Denny JC, Jarvik GP, eMERGE Network, Crosslin DR. The eMERGE genotype set of 83,717 subjects imputed to ~40?million variants genome wide and association with the herpes zoster medical record phenotype. Genet Epidemiol. 2019 02; 43(1):63-81. PMID: 30298529; PMCID: PMC6375696.
      Citations: 39     Fields:    Translation:HumansCells
    4. Puckelwartz MJ, McNally EM. Genetic profiling for risk reduction in human cardiovascular disease. Genes (Basel). 2014 Mar 12; 5(1):214-34. PMID: 24705294; PMCID: PMC3978520.
      Citations: 6     Fields:    
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