Recommender Systems (RS) aim to generate personalized ranked lists for each user and are evaluated using ranking metrics. Although personalized ranking is a fundamental aspect of RS, this critical property is often overlooked in the design of model architectures. To address this issue, we propose Rankformer, a ranking-inspired recommendation model. The architecture of Rankformer is inspired by the gradient of the ranking objective, embodying a unique (graph) transformer architecture --- it leverages global information from all users and items to produce more informative representations and employs specific attention weights to guide the evolution of embeddings towards improved ranking performance. We further develop an acceleration algorithm for Rankformer, reducing its complexity to a linear level with respect to the number of positive instances. Extensive experimental results demonstrate that Rankformer outperforms state-of-the-art methods. The code is available at https://github.com/StupidThree/Rankformer.

Graph Neural Networks (GNNs) have become a prominent approach for learning from graph-structured data. However, their effectiveness can be significantly compromised when the graph structure is suboptimal. To address this issue, Graph Structure Learning (GSL) has emerged as a promising technique that refines node connections adaptively. Nevertheless, we identify two key limitations in existing GSL methods: 1) Most methods primarily focus on node similarity to construct relationships, while overlooking the quality of node information. Blindly connecting low-quality nodes and aggregating their ambiguous information can degrade the performance of other nodes. 2) The constructed graph structures are often constrained to be symmetric, which may limit the model's flexibility and effectiveness.

In recommender systems, most graph-based methods focus on positive user feedback, while overlooking the valuable negative feedback. Integrating both positive and negative feedback to form a signed graph can lead to a more comprehensive understanding of user preferences. However, the existing efforts to incorporate both types of feedback are sparse and face two main limitations: 1) They process positive and negative feedback separately, which fails to holistically leverage the collaborative information within the signed graph; 2) They rely on MLPs or GNNs for information extraction from negative feedback, which may not be effective. To overcome these limitations, we introduceSIGformer, a new method that employs the transformer architecture to sign-aware graph-based recommendation. SIGformer incorporates two innovative positional encodings that capture the spectral properties and path patterns of the signed graph, enabling the full exploitation of the entire graph. Our extensive experiments across five real-world datasets demonstrate the superiority of SIGformer over state-of-the-art methods. The code is available at https://github.com/StupidThree/SIGformer.

Accurate prediction of molecular properties is an important topic in drug discovery. Recent works have developed various representation schemes for molecular structures to capture different chemical information in molecules. The atom and motif can be viewed as hierarchical molecular structures that are widely used for learning molecular representations to predict chemical properties. Previous works have attempted to exploit both atom and motif to address the problem of information loss in single representation learning for various tasks. To further fuse such hierarchical information, the correspondence between learned chemical features from different molecular structures should be considered. Herein, we propose a novel framework for molecular property prediction, called hierarchical molecular graph neural networks (HimGNN). HimGNN learns hierarchical topology representations by applying graph neural networks on atom- and motif-based graphs. In order to boost the representational power of the motif feature, we design a Transformer-based local augmentation module to enrich motif features by introducing heterogeneous atom information in motif representation learning. Besides, we focus on the molecular hierarchical relationship and propose a simple yet effective rescaling module, called contextual self-rescaling, that adaptively recalibrates molecular representations by explicitly modelling interdependencies between atom and motif features. Extensive computational experiments demonstrate that HimGNN can achieve promising performances over state-of-the-art baselines on both classification and regression tasks in molecular property prediction.