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Updated: Sep 17, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Proteome-wide prediction of the mode of inheritance and molecular mechanisms underlying genetic diseases using
Ali Saadat1,2, Jacques Fellay1,2,3
1School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Abstract:
Genetic diseases can be classified according to their modes of inheritance and their underlying molecular mechanisms. Autosomal dominant disorders often result from DNA variants that cause loss-of-function, gain-of-function, or dominant-negative effects, while autosomal recessive diseases are primarily linked to loss-of-function variants. In this study, we introduce a graph-of-graphs approach that leverages protein-protein interaction networks and high-resolution protein structures to predict the mode of inheritance of diseases caused by variants in autosomal genes and to classify dominant-associated proteins based on their functional effect. Our approach integrates graph neural networks, structural interactomics, and topological network features to provide proteome-wide predictions, thus offering a scalable method for understanding genetic disease mechanisms.
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