With your support, we have been able to fund outstanding research, leading toward cures and improved quality of life for children with cancer. Browse through more than 1,000 funded projects below.
Use the search tool to refine your results. You can also click on a heading to sort by project title, institution name, or year the grant was awarded. Click on the project title to read more information.
You can learn about ALSF's grant review process here.
ALSF Funded Research Projects
|Project Title||Institution / Principal Investigator(s)||Grant Type||Year||State|
|Single-cell Profiling of Early T-cell Precursor Acute Lymphoblastic Leukemia||Children's Hospital of Philadelphia / David Teachey, MD and Kai Tan, PhD||Single-cell Pediatric Cancer Atlas Grant||2019||Pennsylvania|
|Single-cell Gene Expression and Cytosine Modification Profiling in Pediatric Central Nervous System Tumors||Dartmouth College / Brock Christensen, PhD||Single-cell Pediatric Cancer Atlas Grant||2019||New Hampshire|
|Investigating phase separated condensates in FPD to MDS/AML progression||Broad Institute / Zuzana Tothova, MD/PhD||RUNX1 Early Career Investigator Grants||2019||Massachusetts|
|Assessing clonal fitness and mechanisms of clonal evolution in FPD-MN||Memorial Sloan-Kettering Cancer Center / Wenbin Xiao, MD/PhD||RUNX1 Early Career Investigator Grants||2020||New York|
|Cell Line and Xenograft Repository||Texas Tech University Health Sciences Center / Patrick Reynolds, MD/PhD||Catalyst Grants||2014||Texas|
|Targeting Spinal Ependymoma and Other Gliomas Using Novel Genetically Defined Models||The Johns Hopkins University School of Medicine / Charles Eberhart, MD, PhD||Catalyst Grants||2019||Maryland|
|Role of Inflammatory Microenvironment in Clonal evolution and Progression from FPD to AML||Oregon Health & Science University / Anupriya Agarwal, PhD||Familial RUNX1 Research Grants||2017||Oregon|
|Restoring RUNX1 Levels in FPD/AML||University of Washington, Seattle / Marshall Horwitz, MD/PhD||Familial RUNX1 Research Grants||2016||Washington|
|Characterization of Pre-Leukemia Associated with Familial RUNX1 Mutations||Stanford University / Ravi Majeti, MD/PhD||Familial RUNX1 Research Grants||2016||California|
|Identifying Therapeutic Targets to Prevent Progression of Familial RUNX1 Disorder to AML Using Novel iPSC Models||Icahn School of Medicine at Mount Sinai / Eirini Papapetrou, MD/PhD||Familial RUNX1 Research Grants||2016||New York|