Restoring RUNX1 deficiency in <i>RUNX1</i> familial platelet disorder by inhibiting its degradationMichelle C. Krutein, Marshall S. Horwitz, Sara Borst et al.|Blood Advances|2021Cited by 18
Use of somatic mutations to quantify random contributions to mouse developmentWenyu Zhou, Marshall S. Horwitz, Yunbing Tan et al.|BMC Genomics|2013Cited by 13
Simultaneous brain cell type and lineage determined by scRNA-seq reveals stereotyped cortical developmentDonovan J. Anderson, Marshall S. Horwitz, Florian M. Pauler et al.|Cell Systems|2022Cited by 10
Activating PAX gene family paralogs to complement PAX5 leukemia driver mutationsMatthew R. Hart, Marshall S. Horwitz, Tobias Neff et al.|PLoS Genetics|2018Cited by 7