G-MIND: An End-to-End Multimodal Imaging-Genetics Framework for Biomarker Identification and Disease Classification
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Abstract (arXiv)
We propose a novel deep neural network architecture to integrate imaging and genetics data, as guided by diagnosis, that provides interpretable biomarkers. Our model consists of an encoder, a decoder and a classifier. The encoder learns a non-linear subspace shared between the input data modalities. The classifier and the decoder act as regularizers to ensure that the low-dimensional encoding captures predictive differences between patients and controls. We use a learnable dropout layer to extract interpretable biomarkers from the data, and our unique training strategy can easily accommodate missing data modalities across subjects. We have evaluated our model on a population study of schizophrenia that includes two functional MRI (fMRI) paradigms and Single Nucleotide Polymorphism (SNP) data. Using 10-fold cross validation, we demonstrate that our model achieves better classification accuracy than baseline methods, and that this performance generalizes to a second dataset collected at a different site. In an exploratory analysis we further show that the biomarkers identified by our model are closely associated with the well-documented deficits in schizophrenia.
Key facts. Cited by 7 papers in the map (data through 7 Oct 2026). Builds on 6 of its 30 references that are in the map. First posted on arXiv 27 Jan 2021.
Builds on
6 of 30 references.
References · 6
- 2014Adam: A Method for Stochastic Optimizationcited by 36,960
- 2015Dropout as a Bayesian Approximation: Representing Model Uncertainty in Deep Learningcited by 4,416
- 2015Delving Deep into Rectifiers: Surpassing Human-Level Performance on ImageNet Classificationcited by 3,590
- 2016Categorical Reparameterization with Gumbel-Softmaxcited by 2,708
- 2017Concrete Dropoutcited by 227
- 2017Multimodal deep learning approach for joint EEG-EMG data compression and classificationcited by 7
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Citing papers per year: 2021: 1; 2022: 2; 2023: 0; 2024: 1; 2025: 1; 2026: 2.
7 papers.
- 2022Deep Multi-modal Fusion of Image and Non-image Data in Disease Diagnosis and Prognosis: A Reviewcited by 37
- 2024Review of multimodal machine learning approaches in healthcarecited by 30
- 2022Survival Prediction of Brain Cancer with Incomplete Radiology, Pathology, Genomics, and Demographic Datacited by 25
- 2021Multi-modality fusion using canonical correlation analysis methods: Application in breast cancer survival prediction from histology and genomicscited by 4
- 2025Learning Explainable Imaging-Genetics Associations Related to a Neurological Disordercited by 1
- 2026AdaFuse: Adaptive Multimodal Fusion for Lung Cancer Risk Prediction via Reinforcement Learningcited by 0
- 2026CALM: Interpretable Cross-Modal Alignment for Biomarker Discovery from Unpaired Datacited by 0
- 2026CALM: Interpretable Cross-Modal Alignment for Biomarker Discovery from Unpaired Data2 Jul 2026
- 2026AdaFuse: Adaptive Multimodal Fusion for Lung Cancer Risk Prediction via Reinforcement Learning30 Jan 2026
- 2025Learning Explainable Imaging-Genetics Associations Related to a Neurological Disorder22 Aug 2025
- 2024Review of multimodal machine learning approaches in healthcare4 Feb 2024
- 2022Deep Multi-modal Fusion of Image and Non-image Data in Disease Diagnosis and Prognosis: A Review25 Mar 2022
- 2022Survival Prediction of Brain Cancer with Incomplete Radiology, Pathology, Genomics, and Demographic Data8 Mar 2022
- 2021Multi-modality fusion using canonical correlation analysis methods: Application in breast cancer survival prediction from histology and genomics27 Nov 2021