Demo Data from VLDB 2026 / reviewers in the wild / expert
Louise Hull
dblp:324/8053 · also M. Louise Hull, Mary Louise Hull
· DBLP profile ↗
5ranked-venue papers
0as first author
5since 2021 · last 2026
0000-0003-1813-3971ORCID · verified
Domains — the database's venue-derived domains; a paper can count in several
Graphics, computer vision, multimedia, augmented reality and games · 4 · 4 since 2021Artificial intelligence and machine learning · 3 · 3 since 2021Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Artificial intelligence
2 papers |
Representation and self-supervised learning · 50% Trustworthy machine learning · 50% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Machine learning › Representation and self-supervised learning
multimodal representation learning |
1.2 | 2 | 2023 | Multi-Modal Learning with Missing Modality via Shared-Specific Feature Modelling · CVPR 2023 Uncertainty-Aware Multi-modal Learning via Cross-Modal Random Network Prediction · ECCV (37) 2022 |
Machine learning › Trustworthy machine learning › learning with incomplete data
missing modality |
0.7 | 1 | 2023 | Multi-Modal Learning with Missing Modality via Shared-Specific Feature Modelling · CVPR 2023 |
Machine learning › Trustworthy machine learning
uncertainty estimation |
0.6 | 1 | 2022 | Uncertainty-Aware Multi-modal Learning via Cross-Modal Random Network Prediction · ECCV (37) 2022 |
Methods — techniques the papers use, named apart from their topics
shared-specific feature modeling · 0.7residual feature fusion · 0.7distribution alignment · 0.7cross-modal random network prediction · 0.6
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2026 | Unpaired multi-modal multi-label learning for detecting endometriosis signsabstractEndometriosis is a widespread gynecological disorder causing severe pain and infertility, with diagnosis currently relying on slow, costly, and risky laparoscopy. This highlights the critical need for non-invasive imaging diagnostics using transvaginal ultrasound (TVUS) and magnetic resonance imaging (MRI). A key challenge is that patients typically receive only one scan modality in practice, despite TVUS and MRI offering differing diagnostic strengths for endometriosis signs like Pouch of Douglas (POD) obliteration and bowel nodules (BN). Previous work partially addressed this challenge by leveraging unpaired multi-modal data for detecting a single marker: Pouch of Douglas (POD) obliteration. However, this is restrictive because endometriosis signs, such as POD obliteration and bowel nodules (BN), often provide correlated diagnostic cues. Capturing these correlations is essential for accurate detection of endometriosis imaging signs, particularly when combined with multi-modal learning, as each modality offers complementary strengths for different signs. To overcome these limitations, we propose EndoFusion, a novel unpaired multi-modal, multi-label learning framework that enables the detection of POD and BN from TVUS and MRI. Our approach introduces three key innovations: (1) label-based pairing, mixup, and cross-modal feature exchange for robust single-modality inference; (2) Dynamic Mutual Knowledge Distillation (DMKD), which adaptively selects teachers using a worst-student-oriented strategy for effective cross-modal transfer; and (3) label correlations modeling with multi-head attention and a specialized loss to handle imbalance and boost accuracy. This design ensures that knowledge from the superior modality and from co-occurring signs is effectively transferred, mitigating modality-specific weaknesses and improving robustness in imaging sign detection. Experiments on our endometriosis dataset show that our method significantly outperforms all comparison methods, achieving an average AUC of 0.827 (95% CI: 0.790-0.861) when evaluated using single-modality inference. These results represent an initial proof-of-concept toward multi-modal, non-invasive assessment of selected endometriosis imaging signs from MRI and TVUS. Hu Wang 0005, Yutong Xie 0001, Minh-Son To, Steven Knox, Mathew Leonardi, George Condous, Jodie Avery, Louise Hull, Gustavo Carneiro 0001 |
Artif. Intell. Medicine | 9 |
| 2025 | A Novel Perspective for Multi-Modal Multi-Label Skin Lesion ClassificationabstractThe efficacy of deep learning-based Computer-Aided Diagnosis (CAD) methods for skin diseases relies on analyzing multiple data modalities (i.e., clinical+dermoscopic images, and patient metadata) and addressing the challenges of multi-label classification. Current approaches tend to rely on limited multi-modal techniques and treat the multi-label problem as a multiple multi-class problem, overlooking issues related to imbalanced learning and multi-label correlation. This paper introduces the innovative Skin Lesion Classifier, utilizing a Multi-modal Multilabel TransFormer-based model (SkinM2Former). For multi-modal analysis, we introduce the Tri-Modal Cross-attention Transformer (TMCT) that fuses the three image and metadata modalities at various feature levels of a transformer encoder. For multi-label classification, we introduce a multi-head attention (MHA) module to learn multi-label correlations, complemented by an optimisation that handles multi-label and imbalanced learning problems. SkinM2Former achieves a mean average accuracy of 77.27% and a mean diagnostic accuracy of 77.85% on the public Derm7pt dataset, outperforming state-of-the-art (SOTA) methods. Yutong Xie 0001, Hu Wang 0005, Jodie Avery, Louise Hull, Gustavo Carneiro 0001 |
WACV | 5 |
| 2023 | Multi-Modal Learning with Missing Modality via Shared-Specific Feature ModellingabstractThe missing modality issue is critical but non-trivial to be solved by multi-modal models. Current methods aiming to handle the missing modality problem in multi-modal tasks, either deal with missing modalities only during evaluation or train separate models to handle specific missing modality settings. In addition, these models are designed for specific tasks, so for example, classification models are not easily adapted to segmentation tasks and vice versa. In this paper, we propose the Shared-Specific Feature Modelling (ShaSpec) method that is considerably simpler and more effective than competing approaches that address the issues above. ShaSpec is designed to take advantage of all available input modalities during training and evaluation by learning shared and specific features to better represent the input data. This is achieved from a strategy that relies on auxiliary tasks based on distribution alignment and domain classification, in addition to a residual feature fusion procedure. Also, the design simplicity of ShaSpec enables its easy adaptation to multiple tasks, such as classification and segmentation. Experiments are conducted on both medical image segmentation and computer vision classification, with results indicating that ShaSpec outperforms competing methods by a large margin. For instance, on BraTS2018, ShaSpec improves the SOTA by more than 3% for enhancing tumour, 5% for tumour core and 3% for whole tumour.11This work received funding from the Australian Government the through Medical Research Futures Fund: Primary Health Care Research Data Infrastructure Grant 2020 and from Endometriosis Australia. G.C. was supported by Australian Research Council through grant FT190100525. Hu Wang 0005, Yuanhong Chen, Congbo Ma, Jodie Avery, Louise Hull, Gustavo Carneiro 0001 |
CVPR | 5 |
| 2023 | Learnable Cross-modal Knowledge Distillation for Multi-modal Learning with Missing Modality
Hu Wang 0005, Congbo Ma, Jodie Avery, Louise Hull, Gustavo Carneiro 0001 |
MICCAI (4) | 6 |
| 2022 | Uncertainty-Aware Multi-modal Learning via Cross-Modal Random Network Prediction
Hu Wang 0005, Yuanhong Chen, Congbo Ma, Jodie Avery, Louise Hull, Gustavo Carneiro 0001 |
ECCV (37) | 6 |