Wing Hung Wong

University of California, Los Angeles — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

93h-index38.9kcitations409works10.22yr avg
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Research Topics

Gene expression and cancer classification(65), Genomics and Chromatin Dynamics(59), Statistical Methods and Inference(44), Bayesian Methods and Mixture Models(38), Single-cell and spatial transcriptomics(36)

Publications406 total

Optimal designs for discrete-time survival models with competing risks
Lifetime Data Analysis·2026Open Access
Overdischarge of Spent Lithium Ion Batteries Induced Copper Deposition Onto Cathode for Better Upcycling
Battery energy·2026Open Access
Geometric Partition for Billion-Scale Approximate Nearest Neighbor Search
IEEE Transactions on Knowledge and Data Engineering·2026
Steering Protein Generative Models at Test-Time for Guided AAV2 Capsid Design
2025Open Access
Modeling combinatorial regulation from single-cell multi-omics provides regulatory units underpinning cell type landscape using cRegulon
Genome biology·2025Open Access
ProVADA: Generation of Subcellular Protein Variants via Ensemble-Guided Test-Time Steering
2025
Improving polygenic prediction from whole-genome sequencing data by leveraging predicted epigenomic features
Proceedings of the National Academy of Sciences·2025· 1 citedOpen Access
Likelihood-Free Adaptive Bayesian Inference via Nonparametric Distribution Matching
arXiv (Cornell University)·2025Open Access
Human stem cells with in vivo high plasticity generated by cell–cell communication
Proceedings of the National Academy of Sciences·2025· 1 citedOpen Access
An AI-powered Bayesian generative modeling approach for causal inference in observational studies
arXiv (Cornell University)·2025Open Access
Steering protein generative models at test-time for guided AAV2 capsid design
Faculty of 1000 Research Ltd·2025Open Access
EpiGePT: a pretrained transformer-based language model for context-specific human epigenomics
Genome biology·2024· 20 citedOpen Access
How to improve polygenic prediction from whole-genome sequencing data by leveraging predicted epigenomic features?
2024· 1 citedOpen Access
Leveraging genomic large language models to enhance causal genotype-brain-clinical pathways in Alzheimer’s disease
2024· 3 citedOpen Access
80. IMPLICATION OF COMPLEX STRUCTURAL GENOME VARIATION IN THE GENETIC ARCHITECTURE OF NEUROPSYCHIATRIC DISORDERS: INSIGHTS FROM HUMAN POPULATION ANALYSIS AND FROM POSTMORTEM BRAINS OF INDIVIDUALS WITH PSYCHIATRIC DISORDERS
European Neuropsychopharmacology·2024
Prioritizing disease-related rare variants by integrating gene expression data
PLoS Genetics·2024· 3 citedOpen Access
Resolving the 22q11.2 deletion using CTLR-Seq reveals chromosomal rearrangement mechanisms and individual variance in breakpoints
Proceedings of the National Academy of Sciences·2024· 3 citedOpen Access
An encoding generative modeling approach to dimension reduction and covariate adjustment in causal inference with observational studies
Proceedings of the National Academy of Sciences·2024· 6 citedOpen Access
Prioritizing disease-related rare variants by integrating gene expression data
Research Square (Research Square)·2024Open Access
Author Correction: Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer
Nature Communications·2024· 1 citedOpen Access
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Frequent Co-authors

Jun S. Liu(5), Hui Jiang(5), Hongkai Ji(4), Kin Fai Au(4), Eric E. Schadt(4), Martin A. Tanner(3), Cheng Li(3), Augustine Kong(3), Xiaotong Shen(3), Xianghong Jasmine Zhou(3), Andrew P. McMahon(3), Cheng Li(2), Cheng Li(2), Griffin M. Weber(2), Wenxiu Ma(2), Pegah Tootoonchi Afshar(2), L. Lee(2), Jason G. Underwood(2), Qing Zhou(2), Faming Liang(2)