Kai Wang
Orcid: 0000-0002-5585-982XAffiliations:
- University of Pennsylvania, Department of Pathology, Philadelphia, PA, USA
- Columbia University, Department of Biomedical Informatics, New York, NY, USA (2016 - 2017)
- University of Southern California, Zilkha Neurogenetic Institute, Los Angeles, CA, USA (2010 - 2016)
- University of Pennsylvania, Department of Genetics, Philadelphia, PA, USA (2006 - 2008)
- University of Washington, Seattle, WA, USA (PhD 2005)
According to our database1,
Kai Wang authored at least 20 papers
between 2005 and 2026.
Collaborative distances:
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Bibliography
2026
Beyond Logit Adjustment: A Residual Decomposition Framework for Long-Tailed Reranking.
CoRR, April, 2026
2025
A comparative evaluation of computational models for RNA modification detection using nanopore sequencing with RNA004 chemistry.
Briefings Bioinform., 2025
PhenoGPT2: A Multimodal Fine-tuned Large Language Models for Phenotype Extraction and Normalization from Clinical Text and Facial Images.
Proceedings of the 16th ACM International Conference on Bioinformatics, 2025
2024
Briefings Bioinform., May, 2024
Enhancing phenotype recognition in clinical notes using large language models: PhenoBCBERT and PhenoGPT.
Patterns, January, 2024
Exploring the reversal curse and other deductive logical reasoning in BERT and GPT-based large language models.
Patterns, 2024
Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders.
npj Digit. Medicine, 2024
2023
Classification of integers based on residue classes via modern deep learning algorithms.
Patterns, December, 2023
Multimodal Machine Learning Combining Facial Images and Clinical Texts Improves Diagnosis of Rare Genetic Diseases.
CoRR, 2023
Not All Large Language Models (LLMs) Succumb to the "Reversal Curse": A Comparative Study of Deductive Logical Reasoning in BERT and GPT Models.
CoRR, 2023
2022
Expediting knowledge acquisition by a web framework for Knowledge Graph Exploration and Visualization (KGEV): case studies on COVID-19 and Human Phenotype Ontology.
BMC Medical Informatics Decis. Mak., 2022
2020
Detecting differential alternative splicing events in scRNA-seq with or without Unique Molecular Identifiers.
PLoS Comput. Biol., 2020
Natural language processing (NLP) tools in extracting biomedical concepts from research articles: a case study on autism spectrum disorder.
BMC Medical Informatics Decis. Mak., 2020
BMC Bioinform., 2020
2019
Nucleic Acids Res., 2019
CircAST: Full-length Assembly and Quantification of Alternatively Spliced Isoforms in Circular RNAs.
Genom. Proteom. Bioinform., 2019
2009
Bioinform., 2009
ATOM: a powerful gene-based association test by combining optimally weighted markers.
Bioinform., 2009
2005
FSSA: a novel method for identifying functional signatures from structural alignments.
Bioinform., 2005