Schaepe, Julia M.
Stanford University
2 papers on CoChatORCID 0000-0003-0416-0469
Most cited papers
- Verified
Neuronal defects in a human cellular model of 22q11.2 deletion syndrome
Khan, T. A., Revah, O., Gordon, A., Yoon, S.-J., Krawisz, A. K., Goold, C., Sun, Y., Kim, C. H., Tian, Y., Li, M.-Y., et al. (2020) · Nature Medicine
Pluripotent Stem Cells ResearchGenomic variations and chromosomal abnormalities
Cited by 186
- Verified
Single-molecule states link transcription factor binding to gene expression
Doughty, B. R., Hinks, M. M., Schaepe, J. M., Marinov, G. K., Thurm, A. R., Rios-Martinez, C., Parks, B. E., Tan, Y., Marklund, E., Dubocanin, D., et al. (2024) · Nature
Genomics and Chromatin DynamicsGene Regulatory Network Analysis
Cited by 42
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