Awards & Honors
Award | Conferred By | Date |
---|---|---|
Catalyst Award | UCSF Innovation Ventures | 2024/2025 |
Mary Anne Koda-Kimble Award | UCSF School of Pharmacy | 2024/2025 |
Junior Faculty Scholar Award | American Society of Hematology | 2023/2024 |
New Frontier Research Award | UCSF Program for Breakthrough Biomedical Research | 2023/2024 |
Career Development Award | American Society of Gene & Cell Therapy | 2022/2022 |
Honorary Mention | Prix Ars Electronica | 2021/2021 |
Star Mentor Award | Stanford Bio-X | 2021/2021 |
Education
Institution | Degree | Dept or School | End Date |
---|---|---|---|
Stanford University | Instructor | Pediatrics | 05/2022 |
Stanford University | Postdoc | Pediatrics | 06/2020 |
Harvard Medical School | Postdoc | Genetics | 05/2016 |
Yale University | PhD | Genetics | 05/2014 |
Grants and Funding
- Enrichment of erythroid cells using truncated EPO receptor | American Society of Hematology | 2023-07-01 - 2026-06-28 | Role: Principal Investigator
- Developing gene therapy strategies to correct a-thalassemia | NIH NHLBI | 2022-01-01 - 2025-12-31 | Role: Co-Investigator
- Developing base editor-mediated correction strategies for a-thalassemia | UCSF | 2023-07-01 - 2025-06-28 | Role: Principal Investigator
- Development of inducible signaling receptors to increase production of clinically relevant cell types | UCSF Program for Breakthrough Biomedical Research | 2023-06-01 - 2024-05-30 | Role: Principal Investigator
- Developing a CRISPR/AAV-mediated genome editing strategy to correct a-thalassemia | American Society of Gene & Cell Therapy | 2022-01-01 - 2022-12-31 | Role: Principal Investigator
Publications
MOST RECENT PUBLICATIONS FROM A TOTAL OF 17
- Enhancement of erythropoietic output by Cas9-mediated insertion of a natural variant in haematopoietic stem and progenitor cells.| | PubMed
- Lineage-tracing hematopoietic stem cell origins in vivo to efficiently make human HLF+ HOXA+ hematopoietic progenitors from pluripotent stem cells.| | PubMed
- Transient inhibition of 53BP1 increases the frequency of targeted integration in human hematopoietic stem and progenitor cells.| | PubMed
- High-efficiency transgene integration by homology-directed repair in human primary cells using DNA-PKcs inhibition.| | PubMed
- Comparative analysis of CRISPR off-target discovery tools following ex vivo editing of CD34+ hematopoietic stem and progenitor cells.| | PubMed
- CRISPR nuclease off-target activity and mitigation strategies.| | PubMed
- Ultra-deep sequencing validates safety of CRISPR/Cas9 genome editing in human hematopoietic stem and progenitor cells.| | PubMed
- Development of β-globin gene correction in human hematopoietic stem cells as a potential durable treatment for sickle cell disease.| | PubMed
- Gene replacement of α-globin with β-globin restores hemoglobin balance in β-thalassemia-derived hematopoietic stem and progenitor cells.| | PubMed
- Improved Genome Editing through Inhibition of FANCM and Members of the BTR Dissolvase Complex.| | PubMed
- Improving the safety of human pluripotent stem cell therapies using genome-edited orthogonal safeguards.| | PubMed
- Highly Efficient and Marker-free Genome Editing of Human Pluripotent Stem Cells by CRISPR-Cas9 RNP and AAV6 Donor-Mediated Homologous Recombination.| | PubMed
- Identification of preexisting adaptive immunity to Cas9 proteins in humans.| | PubMed
- Global Transcriptional Response to CRISPR/Cas9-AAV6-Based Genome Editing in CD34+ Hematopoietic Stem and Progenitor Cells.| | PubMed
- Priming Human Repopulating Hematopoietic Stem and Progenitor Cells for Cas9/sgRNA Gene Targeting.| | PubMed
- Neomorphic effects of recurrent somatic mutations in Yin Yang 1 in insulin-producing adenomas.| | PubMed
- Identification of somatic mutations in parathyroid tumors using whole-exome sequencing.| | PubMed