Selected Publications

Newman, H, Clark, ME, Wong, D, Wu, J, Brodeur, GM, Hunger, SP, Tasian, SK, Olson, TS, Warren, JT, Teachey, DT, Schubert, J, Golenberg, N, Patel, M, Denenberg, EH, Fanning, EA, Chen, J, Luke, T, Charles, S, Gallo, D, Cao, K, Fu, W, Fan, Z, Surrey, LF, Wertheim, G, Luo, M, MacFarland, SP, Li, MM, Zhong, Y. : "Genomic profiling of pediatric hematologic malignancies and diagnosis of cancer predisposition syndromes: Tumor-only versus paired tumor-normal sequencing." Haematologica Feb 2024.

Oved, JS, Gibson, NM, Vanella, K, Elgarten, CW, Wray, L, Warren, JT, Olson, TS.: "Reduced Toxicity Matched Sibling Bone Marrow Transplant Results in Excellent Outcomes for Severe Congenital Neutropenia." Frontiers in Immunology Feb 2024.

Warren, JT, Dickerson, KE, Sharathkumar, AA, Walter, JE, Wilson, DB, Adell, KP, Chen, K, Dubuc, S, MacLeod, R, Peters, K, Steward, M, Taveras, AG, Walkovich, K. : “Mavorixafor for Patients with Chronic Neutropenic Disorders Treated with G-CSF: Preliminary Response Data and G-CSF Dose Reduction in an Ongoing Phase 2, Open-Label, Multicenter Study Support Reduction in G-CSF Dosing.” American Society of Hematology Annual Meeting, San Diego, CA, Poster Dec 2023.

Baiel, J, Wegner, DJ, Wambach, JA, Warren, JT. : "SMC4 Loss of Function is a New Cause of Inherited Bone Marrow Failure." American Society of Hematology Annual Meeting, San Diego, CA, Poster Dec 2023.

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.