Young-Sun Lee
· Associate Professor of Psychology and EducationVerifiedColumbia University · Curriculum & Teaching
Active 2003–2021
About
Young-Sun Lee is an Associate Professor of Psychology and Education at Teachers College, Columbia University. Her scholarly interests include psychometrics, specifically Classical Test Theory, Item Response Theory, and Cognitive Diagnosis Modeling, as well as educational and psychological measurement and applied statistics. She holds a Ph.D. in Educational Psychology with a focus on Educational Measurement & Statistics from the University of Wisconsin-Madison, earned in 2002, and both an M.A. and B.A. from Ewha Womans University in Seoul, South Korea. Her research and academic contributions focus on assessment and testing, with a particular emphasis on diagnostic classification models and their applications in educational measurement. She has co-edited the 'Handbook of Diagnostic Classification Models' and has authored numerous publications exploring the development, evaluation, and application of psychometric models in educational contexts. Lee is actively involved in teaching and mentoring students, with office hours by appointment, and is affiliated with the Human Development Measurement, Evaluation, and Statistics faculty at Teachers College.
Research topics
- Cell biology
- Chemistry
- Endocrinology
- Medicine
- Internal medicine
- Cancer research
- Biology
Selected publications
Complete sequencing of ape genomes
bioRxiv (Cold Spring Harbor Laboratory) · 2024 · 25 citations
- Biology
- Evolutionary biology
- Genetics
We present haplotype-resolved reference genomes and comparative analyses of six ape species, namely: chimpanzee, bonobo, gorilla, Bornean orangutan, Sumatran orangutan, and siamang. We achieve chromosome-level contiguity with unparalleled sequence accuracy (<1 error in 500,000 base pairs), completely sequencing 215 gapless chromosomes telomere-to-telomere. We resolve challenging regions, such as the major histocompatibility complex and immunoglobulin loci, providing more in-depth evolutionary insights. Comparative analyses, including human, allow us to investigate the evolution and diversity of regions previously uncharacterized or incompletely studied without bias from mapping to the human reference. This includes newly minted gene families within lineage-specific segmental duplications, centromeric DNA, acrocentric chromosomes, and subterminal heterochromatin. This resource should serve as a definitive baseline for all future evolutionary studies of humans and our closest living ape relatives.
A resource of targeted mutant mouse lines for 5,061 genes
Nature Genetics · 2021 · 111 citations
- Biology
- Genetics
- Computational biology
Frontiers in Cell and Developmental Biology · 2021 · 12 citations
1st authorCorresponding- Cell biology
- Biology
- Endocrinology
Betacellulin (BTC), an epidermal growth factor family, is known to promote β-cell regeneration. Recently, pancreatic α-cells have been highlighted as a source of new β-cells. We investigated the effect of BTC on α-cells. Insulin+glucagon+ double stained bihormonal cell levels and pancreatic and duodenal homeobox-1 expression were increased in mice treated with recombinant adenovirus-expressing BTC (rAd-BTC) and β-cell-ablated islet cells treated with BTC. In the islets of rAd-BTC-treated mice, both BrdU+glucagon+ and BrdU+insulin+ cell levels were significantly increased, with BrdU+glucagon+ cells showing the greater increase. Treatment of αTC1-9 cells with BTC significantly increased proliferation and cyclin D2 expression. BTC induced phosphorylation of ErbB receptors in αTC1-9 cells. The proliferative effect of BTC was mediated by ErbB-3 or ErbB-4 receptor kinase. BTC increased phosphorylation of ERK1/2, AKT, and mTOR and PC1/3 expression and GLP-1 production in α-cells, but BTC-induced proliferation was not changed by the GLP-1 receptor antagonist, exendin-9. We suggest that BTC has a direct role in α-cell proliferation via interaction with ErbB-3 and ErbB-4 receptors, and these increased α-cells might be a source of new β-cells.
Circulation Research · 2020 · 57 citations
- Biology
- Cancer research
- Cell biology
RATIONALE: . Since proteins from all 3 HHT genes are components of signal transduction of TGF-β (transforming growth factor β) family members, it has been hypothesized that HHT is a disease caused by defects in the ENG-ALK1-SMAD4 linear signaling. However, in vivo evidence supporting this hypothesis is scarce. OBJECTIVE: We tested this hypothesis and investigated the therapeutic effects and potential risks of induced-ALK1 or -ENG overexpression (OE) for HHT. METHODS AND RESULTS: -iKO models. CONCLUSIONS: These data support the notion that ENG and ALK1 form a linear signaling pathway for the formation of a proper arteriovenous network during angiogenesis. We suggest that ALK1 OE or activation can be an effective therapeutic strategy for HHT. Further research is required to study whether this therapy could be translated into treatment for humans.
TMEM100 is a key factor for specification of lymphatic endothelial progenitors
Angiogenesis · 2020 · 24 citations
- Biology
- Cell biology
- Anatomy
European Journal of Cancer · 2020 · 28 citations
- Medicine
- Internal medicine
- Gastroenterology
Frequent coauthors
- 31 shared
Hee‐Sook Jun
- 6 shared
Gyun Jee Song
Catholic Kwandong University
- 5 shared
Seungjin Shin
CTI BioPharma (United States)
- 4 shared
Seong‐Su Moon
Dongguk University WISE
- 4 shared
Minchul Seo
Rural Development Administration
- 4 shared
Meng-Ju Liu
Chung Yuan Christian University
- 4 shared
Mi-Sung Park
Wonkwang University
- 3 shared
Kyeong-Hye Lim
University of Ulsan
Education
- 2002
Ph.D., Educational Psychology (Educational Measurement & Statistics)
University of Wisconsin-Madison
- 1995
M.A., Educational Measurement & Evaluation
Ewha Womans University
- 1992
B.A., Education
Ewha Womans University
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