Hematology & Oncology
Brossier Lab
Nicole M. Brossier, MD, PhD
Division of Hematology & Oncology
Exploring genetic, environmental and developmental influences on glioma formation and cognitive impairment, our lab investigates how these factors shape risk in patients with Neurofibromatosis Type 1 and the broader pediatric population. Using murine models as a platform, we aim to uncover mechanisms driving tumor development and neurodevelopmental changes, identify new strategies for patient risk assessment and discover therapeutic targets. Through this work, we strive to transform understanding and improve outcomes for children affected by NF1 and related conditions.
Child Health and Education Lab
Allison King, MD, MPH, PhD
Division of Hematology & Oncology
Improving outcomes for children with chronic illnesses through research and education, the Child Health and Education Lab focuses on conditions such as Sickle Cell Disease and brain tumors. Led by Allison King, MD, MPH, PhD, our team investigates how environmental, cognitive and psychosocial factors influence health and development. Through partnerships like the Heartland and Southwest Sickle Cell Disease Network, we work to enhance care and quality of life across an eight-state region, while advancing strategies for assessment, transition and long-term support.
Di Paola Lab
Jorge Di Paola, MD
Division of Hematology & Oncology
Discovering genetic and biological determinants of bleeding and thrombosis our lab combines expertise in genomics, bioinformatics and molecular biology to uncover mechanisms underlying disorders such as von Willebrand disease and platelet dysfunction. We develop interactive genomic databases, investigate mutations like NBEAL2 and ETV6 and use CRISPR-modified mice to study hemostasis. Our goal is to translate these insights into novel therapies that improve quality of life for patients with bleeding and thrombotic disorders.
Magee Lab
Jeffrey Magee, MD, PhD
Division of Hematology & Oncology
Critical insights into causes of childhood leukemia and pioneering prevention strategies our lab investigates how leukemias arise from normal blood-forming stem cells, how malignant cells hijack developmental programs and why childhood and adult leukemias differ genetically. Using innovative mouse models we study leukemia evolution during early life and assess how stressors such as chemotherapy contribute to disease. Our goal is to develop new approaches to treat and ultimately prevent childhood leukemia.
Mavers Lab
Melissa Mavers, MD, PhD
Division of Hematology & Oncology
Advancing treatments for blood diseases through innovative cellular therapy research, our center focuses on immune regulation in hematopoietic stem cell transplantation and the development of novel platforms for cell-based therapies. By uncovering mechanisms of immune tolerance, enhancing regulatory immune cells to prevent graft-versus-host disease and designing safer cancer-targeting strategies, we aim to transform HSCT into a more effective and less toxic cure. Our bench-to-bedside approach drives breakthroughs that offer patients long, healthy lives.
Schuettpelz Lab
Laura G. Schuettpelz, MD, PhD
Division of Hematology & Oncology
Exploring inflammation's role in blood cancer and optimizing treatment our lab studies how inflammatory signals affect hematopoietic stem cells and contribute to malignancies. While inflammation is essential for immune defense prolonged exposure can impair stem cell function and drive clonal expansion of mutant cells leading to blood cancers. By understanding these responses we aim to improve stem cell health and develop strategies to prevent hematopoietic malignancies.
Schwartz (Alan) Lab
Alan L. Schwartz, MD, PhD
Division of Hematology & Oncology
Exploring cellular mechanisms that govern protein targeting, degradation and placental development, our laboratory investigates how intracellular pathways maintain homeostasis and regulate receptor-mediated endocytosis. By studying protein processing within endosomal and lysosomal systems and the molecular biology of syncytia formation in placental trophoblasts, we aim to uncover fundamental processes that influence health and disease. Our integrated approach provides insights into cellular regulation with implications for developmental biology and therapeutic innovation.
Shenoy Lab
Shalini Shenoy, MD, MBBS
Division of Hematology & Oncology
Developing safer less toxic hematopoietic stem cell transplantation in children our research focuses on reduced intensity transplantation for hemoglobinopathies such as sickle cell disease and thalassemia using the best available related or alternate donors. Building on multi-center trials like the SCURT trial for severe sickle cell disease and the URTH trial for thalassemia we are now exploring reduced intensity approaches for non-malignant disorders using minimally mismatched marrow or cord blood donors.
Sykes Lab
Stephen Sykes, PhD
Division of Hematology & Oncology
Defining molecular features driving leukemogenesis to improve outcomes in acute leukemia our lab investigates pathways that differ between malignant and healthy cells, promote chemotherapy resistance and support leukemia stem cell biology. Current projects focus on intracellular metabolism including amino acid and nucleotide metabolism, cellular energetics and polyunsaturated fatty acid metabolism, the unfolded protein response and its role in stress adaptation and mitochondrial regulation critical for cancer cell survival. We also examine how these mechanisms influence healthy hematopoietic stem and progenitor cells to guide rational therapeutic strategies.
Taylor Lab
Samuel Taylor, PhD
Investigating how pharmacological agents reshape cellular behavior in health and disease, the Taylor Lab at WashU Medicine studies the mechanisms that drive normal and malignant hematopoiesis to improve treatment outcomes for children with cancer. Childhood leukemia arises when genetic mutations disrupt normal blood cell formation and convert healthy cells into cancerous ones, yet major questions remain about how these mutations hijack cellular machinery to sustain disease. Transcription factors — molecular switches that control gene expression — play a central role in this process. In healthy blood development, they guide the programs that determine cell fate, but in leukemia these switches are corrupted to promote malignant growth. The Taylor Lab works to define how these transcriptional networks are rewired and how they can be therapeutically redirected to restore healthy function.