VLDB 2026 Research / reviewers in the wild / expert
Stephanie A. Harmon
dblp:242/8848 · also Stephanie Anne Harmon
· DBLP profile ↗
11ranked-venue papers
0as first author
10since 2021 · last 2026
0000-0002-2507-2399ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 6 · 5 since 2021Graphics, computer vision, multimedia, augmented reality and games · 5 · 5 since 2021Artificial intelligence and machine learning · 4 · 4 since 2021
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2026 | MAISI-v2: Accelerated 3D High-Resolution Medical Image Synthesis with Rectified Flow and Region-specific Contrastive LossabstractMedical image synthesis is an important topic for both clinical and research applications. Recently, diffusion models have become a leading approach in this area. Despite their strengths, many existing methods struggle with (1) limited generalizability, only working for specific body regions or voxel spacings, (2) slow inference, which is a common issue for diffusion models, and (3) weak alignment with input conditions, which is a critical issue for medical imaging. MAISI, a previously proposed framework, addresses generalizability issues but still suffers from slow inference and limited condition consistency. In this work, we present MAISI-v2, the first accelerated 3D medical image synthesis framework that integrates rectified flow to enable fast and high-quality generation. To further enhance condition fidelity, we introduce a novel region-specific contrastive loss to improve sensitivity to the region of interest. Our experiments show that MAISI-v2 can achieve state-of-the-art image quality with 33× acceleration for latent diffusion models. We also conducted a downstream segmentation experiment to show that the synthetic images can be used for data augmentation. We release our code, training details, model weights, and a GUI demo to facilitate reproducibility and promote further development within the community. Can Zhao 0001, Dong Yang 0005, Yufan He, Yucheng Tang, Benjamin Simon, Mason Belue, Stephanie A. Harmon, Baris Turkbey, Daguang Xu |
AAAI | 8 |
| 2025 | VISTA3D: A Unified Segmentation Foundation Model For 3D Medical ImagingabstractFoundation models for interactive segmentation in 2D natural images and videos have sparked significant interest in building 3D foundation models for medical imaging. However, the domain gaps and clinical use cases for 3D medical imaging require a dedicated model that diverges from existing 2D solutions. Specifically, such foundation models should support a full workflow that can actually reduce human effort. Treating 3D medical images as sequences of 2D slices and reusing interactive 2D foundation models seems straightforward, but 2D annotation is too time-consuming for 3D tasks. Moreover, for large cohort analysis, it’s the highly accurate automatic segmentation models that reduce the most human effort. However, these models lack support for interactive corrections and lack zero-shot ability for novel structures, which is a key feature of "foundation". While reusing pre-trained 2D backbones in 3D enhances zero-shot potential, their performance on complex 3D structures still lags behind leading 3D models. To address these issues, we present VISTA3D, Versatile Imaging SegmenTation and Annotation model, that targets to solve all these challenges and requirements with one unified foundation model. VISTA3D is built on top of the well-established 3D segmentation pipeline, and it is the first model to achieve state-of-the-art performance in both 3D automatic (supporting 127 classes) and 3D interactive segmentation, even when compared with top 3D expert models on large and diverse benchmarks. Additionally, VISTA3D’s 3D interactive design allows efficient human correction, and a novel 3D supervoxel method that distills 2D pre-trained backbones grants VISTA3D top 3D zero-shot performance. We believe the model, recipe, and insights represent a promising step towards a clinically useful 3D foundation model. Code and weights are publicly available at https://github.com/Project-MONAI/VISTA. Yufan He, Yucheng Tang, Andriy Myronenko, Vishwesh Nath, Ziyue Xu 0001, Dong Yang 0005, Can Zhao 0001, Benjamin Simon, Mason Belue, Stephanie A. Harmon, Baris Turkbey, Daguang Xu, Wenqi Li 0001 |
CVPR | 11 |
| 2025 | VILA-M3: Enhancing Vision-Language Models with Medical Expert KnowledgeabstractGeneralist vision language models (VLMs) have made significant strides in computer vision, but they fall short in specialized fields like healthcare, where expert knowledge is essential. Current large multimodal models like Gemini and GPT-4o are insufficient for medical tasks due to their reliance on memorized internet knowledge rather than the nuanced expertise required in healthcare. Meanwhile, existing medical VLMs (e.g. Med-Gemini) often lack expert consultation as part of their design, and many rely on outdated, static datasets that were not created with modern, large deep learning models in mind. VLMs are usually trained in three stages: vision pre-training, vision-language pre-training, and instruction fine-tuning (IFT). IFT has been typically applied using a mixture of generic and healthcare data. In contrast, we propose that for medical VLMs, a fourth stage of specialized IFT is necessary, which focuses on medical data and includes information from domain expert models. Domain expert models developed for medical use are crucial because they are specifically trained for certain clinical tasks, e.g. to detect tumors and classify abnormalities through segmentation and classification, which learn fine-grained features of medical data−features that are often too intricate for a VLM to capture effectively. This paper introduces a new framework, VILA-M3, for medical VLMs that utilizes domain knowledge via expert models. We argue that generic VLM architectures alone are not viable for real-world clinical applications and on-demand usage of domain-specialized expert model knowledge is critical for advancing AI in healthcare. Through our experiments, we show an improved state-of-the-art (SOTA) performance with an average improvement of ~9% over the prior SOTA model Med-Gemini and ~6% over models trained on the specific tasks. Our approach emphasizes the importance of domain expertise in creating precise, reliable VLMs for medical applications. Vishwesh Nath, Wenqi Li 0001, Dong Yang 0005, Andriy Myronenko, Mingxin Zheng, Yao Lu 0006, Hongxu Yin, Yee Man Law, Yucheng Tang, Can Zhao 0001, Ziyue Xu 0001, Yufan He, Stephanie A. Harmon, Benjamin Simon, Greg Heinrich, Stephen R. Aylward, Marc Edgar, Michael Zephyr, Pavlo Molchanov 0001, Baris Turkbey, Holger Roth, Daguang Xu |
CVPR | 15 |
| 2025 | MAISI: Medical AI for Synthetic ImagingabstractMedical imaging analysis faces challenges such as data scarcity, high annotation costs, and privacy concerns. This paper introduces the Medical AI for Synthetic Imaging (MAISI), an innovative approach using the diffusion model to generate synthetic 3D computed tomography (CT) images to address those challenges. MAISI leverages the foundation volume compression network and the latent diffusion model to produce high-resolution CT images (up to a landmark volume dimension of 512 × 512 × 768) with flexible volume dimensions and voxel spacing. By incorporating ControlNet, MAISI can process organ segmentation, including 127 anatomical structures, as additional conditions and enables the generation of accurately annotated synthetic images that can be used for various downstream tasks. Our experiment results show that MAISI's capabilities in generating realistic, anatomically accurate images for diverse regions and conditions reveal its promising potential to mitigate challenges using synthetic data. Can Zhao 0001, Dong Yang 0005, Ziyue Xu 0001, Vishwesh Nath, Yucheng Tang, Benjamin Simon, Mason Belue, Stephanie A. Harmon, Baris Turkbey, Daguang Xu |
WACV | 9 |
| 2024 | A Sparse Convolutional Autoencoder for Joint Feature Extraction and Clustering of Metastatic Prostate Cancer Images
Erolcan Sayar, Helen Richards, Lucas Liu, Baris Turkbey, Michael Haffner, Stephanie A. Harmon |
AIME (2) | 8 |
| 2024 | Automated Detection and Characterization of Small Cell Lung Cancer Liver Metastases on CT
Sophia Ty, Fahmida Haque, Parth Desai, Nobuyuki Takahashi, Usamah Chaudhary, Benjamin Simon, Peter L. Choyke, Anish Thomas, Baris Turkbey, Stephanie A. Harmon |
AIME (2) | 10 |
| 2022 | Auto-FedRL: Federated Hyperparameter Optimization for Multi-institutional Medical Image Segmentation
Dong Yang 0005, Ali Hatamizadeh, An Xu, Ziyue Xu 0001, Wenqi Li 0001, Can Zhao 0001, Daguang Xu, Stephanie A. Harmon, Evrim Turkbey, Baris Turkbey, Bradford J. Wood, Francesca Patella, Elvira Stellato, Gianpaolo Carrafiello, Vishal M. Patel, Holger Roth |
ECCV (21) | 9 |
| 2021 | Federated learning improves site performance in multicenter deep learning without data sharingabstractOBJECTIVE: To demonstrate enabling multi-institutional training without centralizing or sharing the underlying physical data via federated learning (FL). MATERIALS AND METHODS: Deep learning models were trained at each participating institution using local clinical data, and an additional model was trained using FL across all of the institutions. RESULTS: We found that the FL model exhibited superior performance and generalizability to the models trained at single institutions, with an overall performance level that was significantly better than that of any of the institutional models alone when evaluated on held-out test sets from each institution and an outside challenge dataset. DISCUSSION: The power of FL was successfully demonstrated across 3 academic institutions while avoiding the privacy risk associated with the transfer and pooling of patient data. CONCLUSION: Federated learning is an effective methodology that merits further study to enable accelerated development of models across institutions, enabling greater generalizability in clinical use. Karthik Sarma, Stephanie A. Harmon, Thomas Sanford, Holger Roth, Ziyue Xu 0001, Jesse Tetreault, Daguang Xu, Mona Flores, Alex G. Raman, Rushikesh Kulkarni, Bradford J. Wood, Peter L. Choyke, Alan Priester, Leonard S. Marks, Steven S. Raman, Dieter R. Enzmann, Baris Turkbey, William Speier, Corey W. Arnold |
J. Am. Medical Informatics Assoc. | 2 |
| 2021 | Federated semi-supervised learning for COVID region segmentation in chest CT using multi-national data from China, Italy, Japan
Dong Yang 0005, Ziyue Xu 0001, Wenqi Li 0001, Andriy Myronenko, Holger Roth, Stephanie A. Harmon, Sheng Xu 0001, Baris Turkbey, Evrim Turkbey, Xiaosong Wang 0001, Wentao Zhu 0001, Gianpaolo Carrafiello, Francesca Patella, Maurizio Cariati, Hirofumi Obinata, Hitoshi Mori, Kaku Tamura, Peng An 0002, Bradford J. Wood, Daguang Xu |
Medical Image Anal. | 6 |
| 2021 | Multi-Domain Image Completion for Random Missing Input DataabstractMulti-domain data are widely leveraged in vision applications taking advantage of complementary information from different modalities, e.g., brain tumor segmentation from multi-parametric magnetic resonance imaging (MRI). However, due to possible data corruption and different imaging protocols, the availability of images for each domain could vary amongst multiple data sources in practice, which makes it challenging to build a universal model with a varied set of input data. To tackle this problem, we propose a general approach to complete the random missing domain(s) data in real applications. Specifically, we develop a novel multi-domain image completion method that utilizes a generative adversarial network (GAN) with a representational disentanglement scheme to extract shared content encoding and separate style encoding across multiple domains. We further illustrate that the learned representation in multi-domain image completion could be leveraged for high-level tasks, e.g., segmentation, by introducing a unified framework consisting of image completion and segmentation with a shared content encoder. The experiments demonstrate consistent performance improvement on three datasets for brain tumor segmentation, prostate segmentation, and facial expression image completion respectively. Liyue Shen, Wentao Zhu 0001, Xiaosong Wang 0001, Lei Xing 0001, John M. Pauly, Baris Turkbey, Stephanie A. Harmon, Thomas Sanford, Sherif Mehralivand, Peter L. Choyke, Bradford J. Wood, Daguang Xu |
IEEE Trans. Medical Imaging | 7 |
| 2020 | Generalizing Deep Learning for Medical Image Segmentation to Unseen Domains via Deep Stacked TransformationabstractRecent advances in deep learning for medical image segmentation demonstrate expert-level accuracy. However, application of these models in clinically realistic environments can result in poor generalization and decreased accuracy, mainly due to the domain shift across different hospitals, scanner vendors, imaging protocols, and patient populations etc. Common transfer learning and domain adaptation techniques are proposed to address this bottleneck. However, these solutions require data (and annotations) from the target domain to retrain the model, and is therefore restrictive in practice for widespread model deployment. Ideally, we wish to have a trained (locked) model that can work uniformly well across unseen domains without further training. In this paper, we propose a deep stacked transformation approach for domain generalization. Specifically, a series of n stacked transformations are applied to each image during network training. The underlying assumption is that the "expected" domain shift for a specific medical imaging modality could be simulated by applying extensive data augmentation on a single source domain, and consequently, a deep model trained on the augmented "big" data (BigAug) could generalize well on unseen domains. We exploit four surprisingly effective, but previously understudied, image-based characteristics for data augmentation to overcome the domain generalization problem. We train and evaluate the BigAug model (with n=9 transformations) on three different 3D segmentation tasks (prostate gland, left atrial, left ventricle) covering two medical imaging modalities (MRI and ultrasound) involving eight publicly available challenge datasets. The results show that when training on relatively small dataset (n = 10~32 volumes, depending on the size of the available datasets) from a single source domain: (i) BigAug models degrade an average of 11%(Dice score change) from source to unseen domain, substantially better than conventional augmentation (degrading 39%) and CycleGAN-based domain adaptation method (degrading 25%), (ii) BigAug is better than "shallower" stacked transforms (i.e. those with fewer transforms) on unseen domains and demonstrates modest improvement to conventional augmentation on the source domain, (iii) after training with BigAug on one source domain, performance on an unseen domain is similar to training a model from scratch on that domain when using the same number of training samples. When training on large datasets (n = 465 volumes) with BigAug, (iv) application to unseen domains reaches the performance of state-of-the-art fully supervised models that are trained and tested on their source domains. These findings establish a strong benchmark for the study of domain generalization in medical imaging, and can be generalized to the design of highly robust deep segmentation models for clinical deployment. Ling Zhang 0002, Xiaosong Wang 0001, Dong Yang 0005, Thomas Sanford, Stephanie A. Harmon, Baris Turkbey, Bradford J. Wood, Holger Roth, Andriy Myronenko, Daguang Xu, Ziyue Xu 0001 |
IEEE Trans. Medical Imaging | 5 |