Julia T. Warren, MD PhD

Assistant Professor of Pediatrics (Hematology)
Department: Pediatrics
Graduate Group Affiliations
Contact information
3615 Civic Center Boulevard
Abramson Research Center (ARC) 302C
Philadelphia, PA 19104
Abramson Research Center (ARC) 302C
Philadelphia, PA 19104
Office: 215-590-6189
Email:
warrenjt@chop.edu
warrenjt@chop.edu
Education:
BA (Biological Sciences)
University of Chicago , 2007.
MD
Washington University in Saint Louis, School of Medicine , 2015.
PhD (Immunology)
Washington University in Saint Louis, School of Medicine, 2015.
Permanent linkBA (Biological Sciences)
University of Chicago , 2007.
MD
Washington University in Saint Louis, School of Medicine , 2015.
PhD (Immunology)
Washington University in Saint Louis, School of Medicine, 2015.
Selected Publications
Tollefsen, KM, Jin, H, Connelly, J, Newburger, PE, Walkovich, K, Cadavid, D, Warren, JT. : "Incidence of Serious Infection Events in People with Chronic Neutropenia – Analysis of Real-World Data from Patients in the United States." Clinical Immunology Society Annual Meeting, St. Louis, MO, Poster Apr 2023.Warren JT, Walkovich KJ, Bolyard AA, Dickerson KE, Walter JE, Cadavid D, Chapa E, Chen K, MacLeod R, Peters K, Polisson R, & Dale DC: "Mavorixafor for Patients with Chronic Neutropenic Disorders: Results from a Phase 1b, Open-Label, Multicenter Study." American Society of Hematology Annual Meeting, New Orleans, LA, Oral Presentation. Dec 2022.
Tucker EJ, Baker MJ, Hock DH, Warren JT, Jaillard S, Bell KM, Sreenivasan R, Bakhshalizadeh S, Hanna CA, Caruana NJ, Wortmann SB, Rahman S, Pitceathly RDS, Donadieu J, Alimi A, Launay V, Coppo P, Christin-Maitre S, Robevska G, van den Bergen J, Kline BL, Ayers KL, Stewart PN, Stroud DA, Stojanovski D, Sinclair AH : Premature Ovarian Insufficiency in CLPB Deficiency: Transcriptomic, Proteomic and Phenotypic Insights. The Journal of Clinical Endocrinology and Metabolism 107(12): 3328-3340, Nov 2022.
Warren JT, Di Paola J : “Genetics of Inherited Thrombocytopenia”. Blood 139(22): 3264-3277, Jun 2022.
Srinivas, M, Warren, JT, Wilson, DB, Hulbert, ML. : “Severe Hemolytic Phenotype of HbSS Disease with Concurrent G6PD Deficiency and SPTA1 Mutations.” American Society of Pediatric Hematology/Oncology Annual Meeting, Poster May 2022.
Warren JT, Cupo RR, Wattanasirakul P, Spencer DH, Locke AE, Makaryan V, Bolyard AA, Kingston NK, Kelley ML, Shorter J, Bellanne-Chantelot C, Donadieu J, Dale DC, Link DC : “Heterozygous Variants of CLPB are a Cause of Severe Congenital Neutropenia.” Blood 139(5): 779-791, Feb 2022.
Warren JT, Link DC: “Impaired Myelopoiesis in Congenital Neutropenia: Insights into Clonal and Malignant Hematopoiesis” Hematology American Society of Hematology Education Program 2021(1): 514-520, Dec 2021.
Warren, JT, Kelley, M, Makaryan, V, Bolyard, AA, Dale, D, Link DC. : “Spectrum of Pathogenic Genetic Variants in a Large Cohort of North American Congenital and Cyclic Neutropenia Patients: A Report from the SCNIR.” American Society of Hematology Annual Meeting, Atlanta, GA, Poster Dec 2021.
Warren JT, Kelley M, Makaryan V, Bolyard AA, Dale D, Link DC: “Spectrum of Pathogenic Genetic Variants in a Large Cohort of North American Congenital and Cyclic Neutropenia Patients: A Report from the SCNIR.” American Society of Hematology Annual Meeting, Atlanta, GA, Poster Dec 2021.
Warren, JT: “Two Part Perf” (A Case of Isolated CNS HLH). Pediatric Diagnostic Medicine, A Collection of Cases. Chapter 25, 2021.