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GL-ICNN: An End-To-End Interpretable Convolutional Neural Network for the Diagnosis and Prediction of Alzheimer's Disease2025 arXiv (Cornell University) preprint Medicine Dementia and Cognitive Impairment Research Open access
Wenjie Kang, Lize Corrine Jiskoot, Peter Paul De Deyn, Geert Jan Biessels, Huiberdina L. Koek, Jurgen A.H.R. Claassen, +5 more
0citations -
Computation-Efficient Era: A Comprehensive Survey of State Space Models in Medical Image Analysis2024 arXiv (Cornell University) preprint Computer Science Advanced Neural Network Applications Open access
Moein Heidari, Sina Ghorbani Kolahi, Sanaz Karimijafarbigloo, Bobby Azad, Afshin Bozorgpour, Soheila Hatami, +5 more
4citations -
Deconvolution of cellular subsets in human tissue based on targeted DNA methylation analysis at individual CpG sites2020 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Epigenetics and DNA Methylation Open access
Marco F. Schmidt, Tiago Maié, Edgar Dahl, Ivan G. Costa, Wolfgang Wagner
2citations -
The multifaceted process of human coronary atherosclerotic cap destabilisation2024 bioRxiv (Cold Spring Harbor Laboratory) preprint Immunology and Microbiology Atherosclerosis and Cardiovascular Diseases
Laura E. Bruijn, Natascha Fonseca Neves, Connie M. van Rhijn, Jaap F. Hamming, Antoon van den Bogaerdt, Johannes Lindeman
0citations -
Intelligent Anomaly Detection for Lane Rendering Using Transformer with Self-Supervised Pre-Training and Customized Fine-Tuning2023 arXiv (Cornell University) preprint Computer Science Anomaly Detection Techniques and Applications Open access
Yongqi Dong, Xingmin Lu, Ruohan Li, Wei Song, Bart van Arem, Haneen Farah
0citations -
Elucidating the clinical and molecular spectrum of SMARCC2 -associated NDD in a cohort of 65 affected individuals2023 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Elisabeth Bosch, Bernt Popp, Esther Güse, Cindy D. Skinner, Pleuntje J. van der Sluijs, Isabelle Maystadt, +64 more
0citations -
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein2021 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access
Elke de Boer, Charlotte W. Ockeloen, Rosalie A. Kampen, Juliet E. Hampstead, Alexander J.M. Dingemans, Dmitrijs Rots, +46 more
0citations -
TopoEmbedX: A General Framework for Representation Learning on Topological Domains2026 arXiv (Cornell University) preprint Computer Science Topological and Geometric Data Analysis Open access
Florian Frantzen, Ibrahem ALJabea, Inês Bonacho dos Anjos Henriques-Cadby, Theodore Papamarkou, Mustafa Hajij, Michael T. Schaub
0citations