Yunying Lucy Liu
Senior Research Scientist
Also affiliated: Army Medical University (2020); University of Arkansas Medical Center (2018); University of Alabama at Birmingham (2004–2008); Xinqiao Hospital (2020); Stanford Medicine (2020–2025); UAB Medicine (2004); Institut du cancer Rosalind & Morris Goodman (2024); McGill University (2024); Stanford University (2020–2025)
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Y. Lucy Liu's research has focused on the genomic and molecular underpinnings of juvenile myelomonocytic leukemia (JMML). Her work has investigated the role of specific genetic mutations, such as those in SETBP1 and PTEN, in the prognosis and development of JMML. Liu has also participated in clinical trials, including a Phase II/III trial evaluating the use of a farnesyl transferase inhibitor in JMML patients prior to transplantation. Her research extends to animal models, with recent work exploring updates and challenges in animal models of Diamond-Blackfan anemia. Liu's publication record includes studies on the genomic landscape of JMML and the immune landscape of oncohistone-mutant gliomas. She has co-authored 28 publications, accumulating 558 citations and an h-index of 8. She has collaborated with Peter D. Emanuel at the University of Arkansas for Medical Sciences on shared publications.
Metrics
- h-index: 10
- Publications: 35
- Citations: 657
Positions
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Senior Research Scientist 2019–presentStanford University School of Medicine Pediatrics/Stem Cell Transplantation and Regenerative Medicine ORCID
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Senior Research Scientist publications 2008–2025University of Arkansas for Medical Sciences ORCID
Selected Publications
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Juvenile myelomonocytic leukemia stem cells are sensitive to NK cell–mediated lysis and express targetable antigens (2025)
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Sustained fetal hematopoiesis causes juvenile death from leukemia: evidence from a dual-age–specific mouse model (2020)
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PTEN is indispensable for cells to respond to MAPK inhibitors in myeloid leukemia (2018)
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The Dosage of Pten Is Critical in Determining the Disease Severity - a Mouse Model Differentially Mimicking JMML and CMML (2016)
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JQ1, a Potential Therapeutic Molecule for Myeloid Leukemia with PTEN Deficiency (2016)
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Metabolic history impacts mammary tumor epithelial hierarchy and early drug response in mice (2016)
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The genomic landscape of juvenile myelomonocytic leukemia (2015)
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Timing of the Loss of Pten Is Critical in Determining the Disease Phenotype in Mice- a Mouse Model for Pediatric Mixed MDS/MPN (2014)
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Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia (2014)
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Opposite Effects of M1 and M2 Macrophages on Hematopoietic Stem Cell Self-Renewal and Ex Vivo Expansion (2014)
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Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group (2014)
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Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia (2014)
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Mutations in GATA2 are rare in juvenile myelomonocytic leukemia (2014)
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Mutations In GATA2 Are Rare In Juvenile Myelomonocytic Leukemia (2013)
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Overexpression Of DNMT3a and DNMT3b Is Related To Downregulation Of Mir-29a In Juvenile Myelomonocytic Leukemia (JMML) (2013)
Collaboration Network
Top Collaborators
- The genomic landscape of juvenile myelomonocytic leukemia
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
- Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group
- PTEN deficiency is a common defect in juvenile myelomonocytic leukemia
- Mutations in GATA2 are rare in juvenile myelomonocytic leukemia
Showing 5 of 20 shared publications
- The genomic landscape of juvenile myelomonocytic leukemia
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
- Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group
- Mutations in GATA2 are rare in juvenile myelomonocytic leukemia
- Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia
Showing 5 of 7 shared publications
- Sustained fetal hematopoiesis causes juvenile death from leukemia: evidence from a dual-age–specific mouse model
- JQ1, a Potential Therapeutic Molecule for Myeloid Leukemia with PTEN Deficiency
- Overexpression Of DNMT3a and DNMT3b Is Related To Downregulation Of Mir-29a In Juvenile Myelomonocytic Leukemia (JMML)
- Timing of the Loss of Pten Is Critical in Determining the Disease Phenotype in Mice- a Mouse Model for Pediatric Mixed MDS/MPN
- Mir-183 Over-Expression: A Potential Biomarker for Juvenile Myelomonocytic Leukemia (JMML).
Showing 5 of 7 shared publications
- PTEN is indispensable for cells to respond to MAPK inhibitors in myeloid leukemia
- Sustained fetal hematopoiesis causes juvenile death from leukemia: evidence from a dual-age–specific mouse model
- JQ1, a Potential Therapeutic Molecule for Myeloid Leukemia with PTEN Deficiency
- Overexpression Of DNMT3a and DNMT3b Is Related To Downregulation Of Mir-29a In Juvenile Myelomonocytic Leukemia (JMML)
- Timing of the Loss of Pten Is Critical in Determining the Disease Phenotype in Mice- a Mouse Model for Pediatric Mixed MDS/MPN
Showing 5 of 7 shared publications
- Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group
- PTEN deficiency is a common defect in juvenile myelomonocytic leukemia
- Mutations in GATA2 are rare in juvenile myelomonocytic leukemia
- Author's response to the comments on “PTEN deficiency is a common defect in juvenile myelomonocytic leukemia” [Leuk. Res. (2008) (Epub November 17)]
- CREB Deficiency: A Potential Critical Factor for Selective GM-CSF Hypersensitivity in Juvenile Myelomonocytic Leukemia.
Showing 5 of 6 shared publications
- The genomic landscape of juvenile myelomonocytic leukemia
- Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group
- Mutations in GATA2 are rare in juvenile myelomonocytic leukemia
- Mir-183 Over-Expression: A Potential Biomarker for Juvenile Myelomonocytic Leukemia (JMML).
- Mutations In GATA2 Are Rare In Juvenile Myelomonocytic Leukemia
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
- Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group
- Mutations in GATA2 are rare in juvenile myelomonocytic leukemia
- Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia
- Mutations In GATA2 Are Rare In Juvenile Myelomonocytic Leukemia
- PTEN is indispensable for cells to respond to MAPK inhibitors in myeloid leukemia
- Sustained fetal hematopoiesis causes juvenile death from leukemia: evidence from a dual-age–specific mouse model
- JQ1, a Potential Therapeutic Molecule for Myeloid Leukemia with PTEN Deficiency
- The Dosage of Pten Is Critical in Determining the Disease Severity - a Mouse Model Differentially Mimicking JMML and CMML
- Sustained fetal hematopoiesis causes juvenile death from leukemia: evidence from a dual-age–specific mouse model
- JQ1, a Potential Therapeutic Molecule for Myeloid Leukemia with PTEN Deficiency
- Timing of the Loss of Pten Is Critical in Determining the Disease Phenotype in Mice- a Mouse Model for Pediatric Mixed MDS/MPN
- The Dosage of Pten Is Critical in Determining the Disease Severity - a Mouse Model Differentially Mimicking JMML and CMML
- Sustained fetal hematopoiesis causes juvenile death from leukemia: evidence from a dual-age–specific mouse model
- JQ1, a Potential Therapeutic Molecule for Myeloid Leukemia with PTEN Deficiency
- Timing of the Loss of Pten Is Critical in Determining the Disease Phenotype in Mice- a Mouse Model for Pediatric Mixed MDS/MPN
- The Dosage of Pten Is Critical in Determining the Disease Severity - a Mouse Model Differentially Mimicking JMML and CMML
- The genomic landscape of juvenile myelomonocytic leukemia
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
- Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia
- The genomic landscape of juvenile myelomonocytic leukemia
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
- Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
- Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group
- Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
- Phase II/III trial of a pre-transplant farnesyl transferase inhibitor in juvenile myelomonocytic leukemia: A report from the Children's Oncology Group
- Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia
- PTEN is indispensable for cells to respond to MAPK inhibitors in myeloid leukemia
- CREB Deficiency: A Potential Critical Factor for Selective GM-CSF Hypersensitivity in Juvenile Myelomonocytic Leukemia.
- Restoring Cell Responsiveness to GM-CSF and IL-3 by PTEN Is Via Controlling the Regulation of Egr-1 In TF-1a Cell Line
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