JessicaAnn KangMeznarichMD

PubMed

• Correction to: 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 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
• Erythrokinetic mechanism(s) causing the "late anemia" of hemolytic disease of the fetus and newborn.
  Bahr, T., Moise, K., Lopriore, E., Christensen, R., Ohls, R., Ilstrup, S., Meznarich, J.> ;Journal of Perinatology. 2024 Jan 12
• Severe congenital neutropenia, SRP54 pathogenicity, and a framework for surveillance.
  Elaine M Fan, Jennie Vagher, Jessica A Meznarich, Erin Morales Ubico, Sasidhar Goteti, David Peterson, Ahmad Rayes, Luke D Maese> ;American Journal of Medical Genetics. Part A. 2023 May 1
• Female adolescent with recurrent anemia and thrombocytopenia: Questions.
  Michell Lozano Chinga, Zeinab Afify, Amy Lowichik, Matthew M Grinsell, Meredith Seamon, Jessica A Meznarich> ;Pediatric Nephrology. 2022 Sep 1
• Female adolescent with recurrent anemia and thrombocytopenia: Answers.
  Michell Lozano Chinga, Zeinab Afify, Amy Lowichik, Matthew M Grinsell, Meredith Seamon, Jessica A Meznarich> ;Pediatric Nephrology. 2022 Sep 1
• 2 citations
  Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestry.
  Timothy M. Bahr, Archana M. Agarwal, Jessica Meznarich, Wende L. Prince, Tirzah W.P. Wait, Josef T. Prchal, Robert D. Christensen> ;Blood Cells, Molecules & Diseases. 2021 Nov 4
• 1 citations
  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.
  Jessica Meznarich, Anton Rets, Archana M. Agarwal, Robert D. Christensen, N. Scott Reading, Frans A. Kuypers, Josef T. Prchal> ;American Journal of Hematology. 2021 Sep 29
• 3 citations
  Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR)
  Omar Niss, Robert B. Lorsbach, Mikaela Berger, Satheesh Chonat, Morgan L. McLemore, David Buchbinder, Timothy L. McCavit, Linda G. Shaffer, Jessica Simpson, Jeffrey H ...> ;Blood Cells, Molecules & Diseases. 2021 Mar 1
• Infantile Pyknocytosis: End-Tidal CO, %Micro-R Measurements, Next-Generation Sequencing, and Transfusion Avoidance with Darbepoetin.
  Timothy M. Bahr, Mari C Knudsen, Michell Lozano-Chinga, Archana M. Agarwal, Jessica Meznarich, Robin K. Ohls, Robert D. Christensen> ;Biomedicine Hub. 2020 Dec 11
• 13 citations
  VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects
  Katie G. Seu, Lisa Trump, Sana Emberesh, Robert B. Lorsbach, Clarissa E. Johnson, Jessica Meznarich, Hunter R. Underhill, Stella T. Chou, Haripriya Sakthivel, Nicolas ...> ;American Journal of Human Genetics. 2020 Dec 3
• 5 citations
  A Novel Variant in G6PD (c.1375C>G) Identified from a Hispanic Neonate with Extreme Hyperbilirubinemia and Low G6PD Enzymatic Activity.
  Timothy M. Bahr, Michell Lozano-Chinga, Archana M. Agarwal, Jessica Meznarich, Christian C. Yost, Peng Li, N. Scott Reading, Josef T. Prchal, Robert D. Christensen> ;Neonatology. 2020 Sep 28
• 2 citations
  Dizygotic twins with prolonged jaundice and microcytic, hypochromic, hemolytic anemia with pyropoikilocytosis.
  Timothy M. Bahr, Michell Lozano-Chinga, Archana M. Agarwal, Jessica Meznarich, E Gerday, Jennifer L. Smoot, Ann Taylor, Robert D. Christensen> ;Blood Cells, Molecules & Diseases. 2020 Nov 1
• 4 citations
  Fetal presentation of Congenital Dyserythropoietic Anemia Type 1 with novel compound heterozygous CDAN1 mutations
  Jessica Meznarich, Lauren Draper, Robert D. Christensen, Hassan M. Yaish, Nick D. Luem, Theodore J. Pysher, Grace Jung, Elizabeta Nemeth, Tomas Ganz, Diane M. Ward> ;Blood Cells, Molecules & Diseases. 2018 Jul 1
• 1 citations
  GFI1 functions in transcriptional control and cell fate determination require SNAG domain methylation to recruit LSD1.
  Matthew Velinder, Jason Singer, Diana Bareyan, Jessica Meznarich, Christopher M Tracy, James M Fulcher, David McClellan, Helena Lucente, Sarah Franklin, Sunil Sharma, ...> ;The Biochemical Journal. 2017 Aug 11
• 9 citations
  GFI1 functions in transcriptional control and cell fate determination require SNAG domain methylation to recruit LSD1.
  Matthew Velinder, Jason Singer, Diana Bareyan, Jessica Meznarich, Christopher M Tracy, James M Fulcher, David McClellan, Helena Lucente, Sarah Franklin, Sunil Sharma, ...> ;The Biochemical Journal. 2016 Oct 1
• 7 citations
  Pediatric B-Cell Lymphoma With Lymphoblastic Morphology, TdT Expression, MYC Rearrangement, and Features Overlapping With Burkitt Lymphoma.
  Jessica Meznarich, Rodney R. Miles, Christian N. Paxton, Zeinab Afify> ;Pediatric Blood & Cancer. 2016 May 1
• 28 citations
  Urokinase Plasminogen Activator Induces Pro-Fibrotic/M2 Phenotype in Murine Cardiac Macrophages
  Jessica Meznarich, Laura Malchodi, Deri Helterline, Stephen A. Ramsey, Kate Bertko, Tabitha Plummer, A. R. Plawman, Elizabeth S. Gold, April Stempien-Otero> ;Plos One. 2013 Mar 11
• 19 citations
  The role of macrophage-derived urokinase plasminogen activator in myocardial infarct repair Urokinase attenuates ventricular remodeling
  Elina Minami, Chiara Castellani, Laura Malchodi, Jennifer D. Deem, Kate Bertko, Jessica Meznarich, Monja Dishmon, Charles E. Murry, April Stempien-Otero> ;Journal of Molecular and Cellular Cardiology. 2010 Sep 1
• 36 citations
  Mechanisms of cardiac fibrosis induced by urokinase plasminogen activator.
  April Stempien-Otero, A. R. Plawman, Jessica Meznarich, Teja Dyamenahalli, Goro Otsuka, David A. Dichek> ;The Journal of Biological Chemistry. 2006 Jun 2
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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 Delay
  Jessica Meznarich, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/8/2019