Jessica A. Meznarich

Jessica A. Meznarich

Hematology | Oncology

1950 Circle Of Hope Dr
Salt Lake City, UT 84112

Last Updated: 09/26/2026

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Found 21 publications

Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing.

Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing.

Journal: Blood advances

Published: November 22, 2024

Novel germline JAK2R715T mutation causing PV-like erythrocytosis in 3 generations. Amelioration by Ropeg-Interferon.

Novel germline JAK2R715T mutation causing PV-like erythrocytosis in 3 generations. Amelioration by Ropeg-Interferon.

Journal: American journal of hematology

Published: March 20, 2024

Correction to: Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.

Correction to: Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.

Journal: Journal of clinical immunology

Published: February 29, 2024

Familial autoimmunity and risk of developing immune thrombocytopenia and Evans syndrome.

Familial autoimmunity and risk of developing immune thrombocytopenia and Evans syndrome.

Journal: Pediatric blood & cancer

Published: February 20, 2024

Erythrokinetic mechanism(s) causing the "late anemia" of hemolytic disease of the fetus and newborn.

Erythrokinetic mechanism(s) causing the "late anemia" of hemolytic disease of the fetus and newborn.

Journal: Journal of perinatology : official journal of the California Perinatal Association

Published: October 26, 2023

Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.

Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.

Journal: Journal of clinical immunology

Published: June 09, 2023

Severe congenital neutropenia, SRP54 pathogenicity, and a framework for surveillance.

Severe congenital neutropenia, SRP54 pathogenicity, and a framework for surveillance.

Journal: American journal of medical genetics. Part A

Published: October 28, 2022

Female adolescent with recurrent anemia and thrombocytopenia: Answers.

Female adolescent with recurrent anemia and thrombocytopenia: Answers.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 21, 2022

Female adolescent with recurrent anemia and thrombocytopenia: Questions.

Female adolescent with recurrent anemia and thrombocytopenia: Questions.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 21, 2022

An Infant With Hereditary Fructose Intolerance and a Novel Presentation of Disseminated Intravascular Coagulopathy Following Pyloromyotomy.

An Infant With Hereditary Fructose Intolerance and a Novel Presentation of Disseminated Intravascular Coagulopathy Following Pyloromyotomy.

Journal: Journal of pediatric hematology/oncology

Published: October 26, 2021

Novel, de novo, beta-globin variant with decreased oxygen affinity (HBB:c.317T>A, "Hemoglobin St. George") in a healthy child with low oxygen saturations and anemia.

Novel, de novo, beta-globin variant with decreased oxygen affinity (HBB:c.317T>A, "Hemoglobin St. George") in a healthy child with low oxygen saturations and anemia.

Journal: American journal of hematology

Published: August 14, 2021

Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestry.

Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestry.

Journal: Blood cells, molecules & diseases

Published: June 22, 2021

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Last Updated: 09/26/2026