Emilie S. Zoltick, ScD, MPH
Postdoctoral Fellow (previously held)
Boston University Chobanian & Avedisian School of Medicine
Medicine
Preventive Medicine & Epidemiology




Emilie S. Zotlick holds a ScD and an MPH in Epidemiology. Her research focuses on the reporting of results of genome sequencing healthy adults and also on creating trajectories for the ideal cardiovascular health score among Framingham Heart Study participants. She has presented to the BU community and to the American Society of Human Genetics in Orlando, Florida in October 2017. Emilie has also authored one manuscript titled “ABO blood group and risk of glioma” in Neuro Oncology She has also submitted a manuscript titled “Predispositional Genome Sequencing in Healthy Adults: Design, Participant Characteristics, and Early Outcomes of the PeopleSeq Consortium”.

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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  1. Coughlin CG, Zoltick ES, Stanford FC, Ong MS. Racial and ethnic disparities in clinical trials for pediatric obesity. Obesity (Silver Spring). 2025 Mar; 33(3):560-566. PMID: 39904717
      Article has an altmetric score of 1
  2. Grady LO, Zoltick ES, Zouk H, He W, Perez E, Clarke L, Gold J, Strong A, Sahai I, Yeo J, Green RC, Karaa A, Gold NB. Long-Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I. Am J Med Genet A. 2025 Apr; 197(4):e63940. PMID: 39559959
      Article has an altmetric score of 1
  3. Zoltick ES, Wu AC, Ong MS. Racial and ethnic representation of youth in type 1 diabetes interventional trials. Contemp Clin Trials. 2024 Nov; 146:107703. PMID: 39349217; PMCID: PMC11531383; DOI: 10.1016/j.cct.2024.107703;
     
  4. Platt DM, Blout Zawatsky CL, Christensen KD, Green RC, Hajek C, Hickingbotham MR, Hutchinson AM, LeBlanc JL, Zoltick ES, Jamal L. Primary Care Providers' Experiences With an Active Elective Genetic Testing Program. Health Educ Behav. 2025 Feb; 52(1):28-37. PMID: 39081055
     
  5. Zoltick ES, Bell M, Hickingbotham MR, Wu AC, Galbraith LN, LeBlanc JL, Lu CY, Leonhard JR, Platt DM, Smith HS, Green RC, Hajek C, Christensen KD. Attitudes, knowledge, and risk perceptions of patients who received elective genomic testing as a clinical service. Genet Med. 2024 Oct; 26(10):101200. PMID: 38943480; PMCID: PMC11456384; DOI: 10.1016/j.gim.2024.101200;
     
  6. Adelson SM, Blout Zawatsky CL, Hickingbotham MR, Bell ME, Platt DM, Leonhard JR, Zoltick ES, Hajek CA, Green RC, Christensen KD. Familial communication and cascade testing following elective genomic testing. J Genet Couns. 2025 Feb; 34(1):e1907. PMID: 38757439; PMCID: PMC11568072; DOI: 10.1002/jgc4.1907;
      Article has an altmetric score of 1
  7. Massmann A, Christensen KD, Van Heukelom J, Schultz A, Shaukat MHS, Hajek C, Weaver M, Green RC, Wu AC, Hickingbotham MR, Zoltick ES, Stys A, Stys TP. Clinical impact of preemptive pharmacogenomic testing on antiplatelet therapy in a real-world setting. Eur J Hum Genet. 2024 Aug; 32(8):895-902. PMID: 38424298; PMCID: PMC11291480; DOI: 10.1038/s41431-024-01567-1;
      Article has an altmetric score of 4
  8. Preys CL, Blout Zawatsky CL, Massmann A, Heukelom JV, Green RC, Hajek C, Hickingbotham MR, Zoltick ES, Schultz A, Christensen KD. Attitudes about pharmacogenomic testing vary by healthcare specialty. Pharmacogenomics. 2023 Jul; 24(10):539-549. PMID: 37458095; PMCID: PMC10621761; DOI: 10.2217/pgs-2023-0039;
      Article has an altmetric score of 5
  9. Massmann A, Van Heukelom J, Green RC, Hajek C, Hickingbotham MR, Larson EA, Lu CY, Wu AC, Zoltick ES, Christensen KD, Schultz A. SLCO1B1 gene-based clinical decision support reduces statin-associated muscle symptoms risk with simvastatin. Pharmacogenomics. 2023 May; 24(7):399-409. PMID: 37232094; PMCID: PMC10242433; DOI: 10.2217/pgs-2023-0056;
      Article has an altmetric score of 1
  10. Gold NB, Adelson SM, Shah N, Williams S, Bick SL, Zoltick ES, Gold JI, Strong A, Ganetzky R, Roberts AE, Walker M, Holtz AM, Sankaran VG, Delmonte O, Tan W, Holm IA, Thiagarajah JR, Kamihara J, Comander J, Place E, Wiggs J, Green RC. Perspectives of Rare Disease Experts on Newborn Genome Sequencing. JAMA Netw Open. 2023 May 01; 6(5):e2312231. PMID: 37155167; PMCID: PMC10167563; DOI: 10.1001/jamanetworkopen.2023.12231;
      Article has an altmetric score of 290
Showing 10 of 23 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 23 publications over 10 distinct years, with a maximum of 6 publications in 2024

YearPublications
20131
20173
20181
20192
20201
20213
20221
20234
20246
20251

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