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Office
100 N Mario Capecchi Drive
Primary Children's Medical Center
Salt Lake City, UT 84132Phone+1 801-662-4700Fax+1 801-662-4707- Is this information wrong?
Education & Training
- University of Utah HealthFellowship, Pediatric Hematology/Oncology, 2013 - 2016
- University of Utah HealthResidency, Pediatrics, 2010 - 2013
- University of Washington School of MedicineClass of 2010
Certifications & Licensure
- UT State Medical License 2011 - 2026
- MT State Medical License 2016 - 2025
- NV State Medical License 2023 - 2025
- CO State Medical License 2023 - 2025
- ID State Medical License 2023 - 2024
- WY State Medical License 2023 - 2024
- American Board of Pediatrics Pediatrics
- American Board of Pediatrics Pediatric Hematology-Oncology
Publications & Presentations
PubMed
- Novel germline JAK2mutation causing PV-like erythrocytosis in 3 generations. Amelioration by Ropeg-Interferon.Jihyun Song, Lucie Lanikova, Soo Jin Kim, Nicolas Papadopoulos, Stefan N Constantinescu, Brynn Parsegov, Jaroslav F Prchal, Jessica Meznarich, Josef T Prchal> ;American Journal of Hematology. 2024 Apr 17
- Correction to: Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.Priya K Patel, Michell Lozano Chinga, Melis Yilmaz, Sonia Joychan, Boglarka Ujhazi, Maryssa Ellison, Sumai Gordon, Daime Nieves, Krisztian Csomos, Don Eslin, Zeinab A ...> ;Journal of Clinical Immunology. 2024 Feb 29
- Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.Patel, P., Chinga, M., Yilmaz, M., Joychan, S., Ujhazi, B., Ellison, M., Gordon, S., Nieves, D., Csomos, K., Eslin, D., Afify, Z., Meznarich, J., Bohnsack, J., Walkovi...> ;Journal of Clinical Immunology. 2024 Jan 17
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Abstracts/Posters
- Congenital Dyserythropoietic Anemia Type I Due to Biallelic CDAN1 mutations: Report from the Congenital Dyserythropoietic Anemia Registry (CDAR)Jessica Meznarich, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/9/2019
- VPS4A mutations Cause a Syndrome with Dyserythropoiesis, Hemolytic Anemia, and Neurodevelopmental DelayJessica Meznarich, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/8/2019
Hospital Affiliations
- Primary Children's HospitalSalt Lake City, Utah
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