Sotabase

Career

· Deputy Group Leader, Materials for Energy and Climate Security, Lawrence Livermore National Laboratory2021–
· Staff Scientist, SLAC National Accelerator Laboratory2015–2021
· Postdoctoral Researcher, Stanford University2013–2015
· Bachelor's degree, University of California, Berkeley2007–
· PhD Student, University of California, Berkeley2007–2012

Publications (139)

Heritable GATA2 Mutations Associated with Familial Myelodysplastic Syndrome and Acute Myeloid Leukemia
Nature Genetics · 2011
590
cited
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
Nature Genetics · 2013
291
cited
Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature.
Blood · 2012
280
cited
GATA2 is required for lymphatic vessel valve development and maintenance.
Journal of Clinical Investigation · 2015
197
cited
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.
Blood · 2016
188
cited
Sphingosine kinase-1 enhances endothelial cell survival through a PECAM-1-dependent activation of PI-3K/Akt and regulation of Bcl-2 family members.
Blood · 2005
187
cited
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease.
Blood · 2018
175
cited
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.
Blood Advances · 2020
126
cited
Genomic subtyping and therapeutic targeting of acute erythroleukemia
Nature Genetics · 2019
121
cited
Transcriptional Synergism between Vitamin D-responsive Elements in the Rat 25-Hydroxyvitamin D3 24-Hydroxylase (CYP24) Promoter*
Journal of Biological Chemistry · 1996
119
cited
PPARγ Agonists Ameliorate Endothelial Cell Activation via Inhibition of Diacylglycerol–Protein Kinase C Signaling Pathway: Role of Diacylglycerol Kinase
Circulation Research · 2004
108
cited
ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia.
Journal of Clinical Endocrinology and Metabolism · 2014
106
cited
nl2spec: Interactively Translating Unstructured Natural Language to Temporal Logics with Large Language Models
International Conference on Computer Aided Verification · 2023
105
cited
Effect of disrupted SOX18 transcription factor function on tumor growth, vascularization, and endothelial development.
Journal of the National Cancer Institute · 2006
95
cited
Basal and angiopoietin-1-mediated endothelial permeability is regulated by sphingosine kinase-1.
Blood · 2008
94
cited
Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome
Leukemia · 2010
88
cited
Phenoxodiol, an experimental anticancer drug, shows potent antiangiogenic properties in addition to its antitumour effects
International Journal of Cancer · 2006
79
cited
Myeloid neoplasms with germline DDX41 mutation
International journal of hematology · 2017
78
cited
Teaching Temporal Logics to Neural Networks
International Conference on Learning Representations · 2020
76
cited
Clonal Diversity of Recurrently Mutated Genes in Myelodysplastic Syndromes
2014
73
cited
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