Stanford University
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Caitlin Ang
Casual Employee, Medicine - Med/Gastroenterology and Hepatology
Bio(she/her/hers)
Caitlin is a public health researcher with an MSPH from Johns Hopkins University, focused on women’s and reproductive health outcomes, population-level analysis, and equity-driven research. Her work sits at the intersection of data, policy, and real-world impact—using rigorous methods to understand how systems shape health outcomes across the life course.
Caitlin has experience supporting and leading quantitative and mixed-methods research, including data management and analysis, literature reviews, IRB and regulatory processes, and translating findings into reports, briefs, and academic outputs. She is especially interested in research related to maternal morbidity and mortality, reproductive health access, and structural drivers of health inequities.
She currently works as a research assistant for the Salles Lab at Stanford. Caitlin looks forward to contributing to creating inclusive, accessible spaces through this role by contributing to the Ending Sexual harassment: Teaching of Principal Investigators (E-STOP) Study. -
Lay Teng Ang
Assistant Professor of Urology
BioAs a stem cell biologist, I aim to understand the mechanisms through which stem cells differentiate into progressively specialized cell types and to harness this knowledge to artificially generate pure populations of desired cell types from stem cells. My work over the past ten years has centered on pluripotent stem cells (PSCs, which include embryonic and pluripotent stem cells), which can generate any of the hundreds of diverse cell types in the body. However, it has been notoriously challenging to guide PSCs to differentiate into a pure population of a given cell type. Current differentiation strategies typically generate heterogeneous cell populations unsuitable for basic research or clinical applications. To address this challenge, I mapped the cascade of branching lineage choices through which PSCs differentiate into various endodermal and mesodermal cell types. I then developed effective methods to differentiate PSCs into specific lineages by providing the extracellular signal(s) that specify a given lineage while inhibiting the signals that induce the alternate fate(s), enabling the generation of highly-pure human heart and bone (Loh & Chen et al., 2016; Cell) and liver (Loh & Ang et al., 2014; Cell Stem Cell) from PSCs. My laboratory currently focuses on differentiating human PSCs into liver progenitors (Ang et al., 2018; Cell Reports) and blood vessel cells (Ang et al., 2022; Cell).
I earned my Ph.D. jointly from the University of Cambridge and A*STAR and was subsequently appointed as a Research Fellow and, later, a Senior Research Fellow at the Genome Institute of Singapore. I then moved my laboratory to Stanford University as a Siebel Investigator and Instructor at the Stanford Institute for Stem Cell Biology & Regenerative Medicine. In 2024, I am jointly appointed in the Stanford Department of Urology and Stem Cell Institute as an Assistant Professor.
I am an Additional Ventures Catalyst to Independence Fellow, Bladder Cancer Advocacy Network Career Development Awardee, Faculty Women’s Forum’s Inspiring Early Academic Career Award recipient, and Stanford-HBMC Recognizing Individuals for Support and Empowerment Award recipient. I have mentored over 31 trainees and currently mentor seven lab members, including two postdoctoral fellows, one research assistant, two CIRM interns, and one undergraduate intern.
