Hannah Yong Wen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Hannah Yong Wen has a total of 288 co-authors. Here are the top co-authors by number of shared publications:
Edi Brogi
Department of Pathology and Laboratory Medicine Memorial Sloan Kettering Cancer Center New York New York USA
19 shared publications- Edi Brogi
Department of Pathology and Laboratory Medicine Memorial Sloan Kettering Cancer Center New York New York USA
13 shared publications - Xiaojing Guo
Department of Breast Pathology and Lab, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Breast Cancer Prevention and Therapy of Ministry of Education of China, Tianjin Medical University, Tianjin’s Clinical Research Center for Cancer
11 shared publications - Bingchao Zhao
Guangdong Provincial Key Laboratory of Artificial Intelligence in Medical Image Analysis and Application, Guangdong Provincial People’s Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China
10 shared publications - Changhong Liang
Department of Radiology, Guangdong Provincial People’s Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China
10 shared publications - Cheng Lu
Department of Radiology, Guangdong Provincial People’s Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China
10 shared publications
Latest Publications
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S3 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance, computational efficiency, and storage burden (10× versus 20×, TCGA-Glioma)
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S3 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance, computational efficiency, and storage burden (10× versus 20×, TCGA-Glioma)
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Data from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Despite the impressive performance across a range of applications, current computational pathology (CPath) models face significant diagnostic efficiency challenges due to their reliance on high-magnification whole-slide image analysis. This limitation compromises their clinical utility, especially in time-sensitive diagnostic scenarios and situations requiring efficient data transfer. To address these issues, we developed a computation- and communication-efficient framework called Magnification-Aligned Global-Local Transformer (MAG-GLTrans). The approach substantially reduced computational time, file transfer requirements, and storage overhead by enabling effective analysis using low-magnification inputs. The magnification alignment (MAG) mechanism employed self-supervised learning to bridge the information gap between low- and high-magnification levels by effectively aligning their feature representations. Through extensive evaluation across various fundamental CPath tasks, MAG-GLTrans demonstrated state-of-the-art classification performance while achieving remarkable efficiency gains, including up to a 10.7× reduction in computational time and more than a 20× reduction in file transfer and storage requirements. Furthermore, the versatility of the MAG framework was demonstrated through two significant extensions: (i) its applicability as a feature extractor to enhance the efficiency of any CPath architecture and (ii) its compatibility with existing foundation models, enabling them to process low-magnification inputs with minimal information loss. In a real-world clinical application, computer-assisted telepathology for intraoperative frozen section diagnosis of non–small cell lung carcinoma, MAG-GLTrans effectively recognized distinct tumor morphologies and accurately localized diagnostically relevant regions with low computational and communication costs. Together, these advancements position MAG-GLTrans as a particularly promising solution for time-sensitive applications, especially in the context of intraoperative frozen section diagnosis, in which both accuracy and efficiency are paramount.Significance:MAG-GLTrans is a general-purpose whole-slide image analysis architecture designed for computational pathology applications, including cancer subtyping, metastasis detection, and mutation prediction, that simultaneously optimizes diagnostic capability, computational efficiency, and communication burden.
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessData from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Despite the impressive performance across a range of applications, current computational pathology (CPath) models face significant diagnostic efficiency challenges due to their reliance on high-magnification whole-slide image analysis. This limitation compromises their clinical utility, especially in time-sensitive diagnostic scenarios and situations requiring efficient data transfer. To address these issues, we developed a computation- and communication-efficient framework called Magnification-Aligned Global-Local Transformer (MAG-GLTrans). The approach substantially reduced computational time, file transfer requirements, and storage overhead by enabling effective analysis using low-magnification inputs. The magnification alignment (MAG) mechanism employed self-supervised learning to bridge the information gap between low- and high-magnification levels by effectively aligning their feature representations. Through extensive evaluation across various fundamental CPath tasks, MAG-GLTrans demonstrated state-of-the-art classification performance while achieving remarkable efficiency gains, including up to a 10.7× reduction in computational time and more than a 20× reduction in file transfer and storage requirements. Furthermore, the versatility of the MAG framework was demonstrated through two significant extensions: (i) its applicability as a feature extractor to enhance the efficiency of any CPath architecture and (ii) its compatibility with existing foundation models, enabling them to process low-magnification inputs with minimal information loss. In a real-world clinical application, computer-assisted telepathology for intraoperative frozen section diagnosis of non–small cell lung carcinoma, MAG-GLTrans effectively recognized distinct tumor morphologies and accurately localized diagnostically relevant regions with low computational and communication costs. Together, these advancements position MAG-GLTrans as a particularly promising solution for time-sensitive applications, especially in the context of intraoperative frozen section diagnosis, in which both accuracy and efficiency are paramount.Significance:MAG-GLTrans is a general-purpose whole-slide image analysis architecture designed for computational pathology applications, including cancer subtyping, metastasis detection, and mutation prediction, that simultaneously optimizes diagnostic capability, computational efficiency, and communication burden.
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S7 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Visualization of the features extracted by MAG (CAMELYON16)
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S7 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Visualization of the features extracted by MAG (CAMELYON16)
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S6 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Comparison on different field of views (FOV)
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S6 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Comparison on different field of views (FOV)
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S4 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Comparison with an efficiency baseline ZoomMIL
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S4 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Comparison with an efficiency baseline ZoomMIL
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S5 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance comparing with pathology foundation models (5× versus 20×)
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S5 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance comparing with pathology foundation models (5× versus 20×)
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S2 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance, computational efficiency, and storage burden (5× versus 20×, TCGA-Glioma)
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S2 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance, computational efficiency, and storage burden (5× versus 20×, TCGA-Glioma)
- Open Access
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S1 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance, computational efficiency, and storage burden (10× versus 20×, TCGA-NSCLC, TCGA-Glioma, CAMELYON16)
- 18 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S1 from A Magnification Alignment Framework Enables Computation- and Communication-Efficient Computational Pathology
Classification performance, computational efficiency, and storage burden (10× versus 20×, TCGA-NSCLC, TCGA-Glioma, CAMELYON16)
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Data from A Genomics-Driven Artificial Intelligence–Based Model Classifies Breast Invasive Lobular Carcinoma and Discovers CDH1 Inactivating Mechanisms
Supplementary Figures S1-S5 Supplementary Tables S1-S5
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Data from A Genomics-Driven Artificial Intelligence–Based Model Classifies Breast Invasive Lobular Carcinoma and Discovers CDH1 Inactivating Mechanisms
Supplementary Figures S1-S5 Supplementary Tables S1-S5