| Prediction and interpretation of deleterious coding variants in terms of protein structural stability F Ancien, F Pucci, M Godfroid, M Rooman Scientific reports 8 (1), 4480, 2018 | 89 | 2018 |
| NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia M Coutelier, M Jacoupy, A Janer, F Renaud, N Auger, GV Saripella, ... Brain 145 (4), 1519-1534, 2022 | 19 | 2022 |
| SWOTein: A structure-based approach to predict stability Strengths and Weaknesses of prOTEINs Q Hou, F Pucci, F Ancien, JM Kwasigroch, R Bourgeas, M Rooman Bioinformatics 37 (14), 1963-1971, 2021 | 15 | 2021 |
| b2bTools: online predictions for protein biophysical features and their conservation LP Kagami, G Orlando, D Raimondi, F Ancien, B Dixit, J Gavaldá-García, ... Nucleic acids research 49 (W1), W52-W59, 2021 | 13 | 2021 |
| In Silico Analysis of the Molecular-Level Impact of SMPD1 Variants on Niemann-Pick Disease Severity F Ancien, F Pucci, M Rooman International journal of molecular sciences 22 (9), 4516, 2021 | 8 | 2021 |
| Lexicon Visualization Library and JavaScript for scientific data visualization I Tanyalcin, C Al Assaf, J Ferte, F Ancien, T Khan, G Smits, M Rooman, ... Computing in Science & Engineering 20 (1), 50-65, 2018 | 6 | 2018 |
| Critical assessment of missense variant effect predictors on disease-relevant variant data R Rastogi, R Chung, S Li, C Li, K Lee, J Woo, DW Kim, C Keum, G Babbi, ... bioRxiv, 2024.06. 06.597828, 2024 | 4 | 2024 |
| MutaFrame—an interpretative visualization framework for deleteriousness prediction of missense variants in the human exome F Ancien, F Pucci, W Vranken, M Rooman Bioinformatics 38 (1), 265-266, 2022 | 4 | 2022 |
| Visualization of automatically combined disease maps and pathway diagrams for rare diseases P Gawron, D Hoksza, J Piñero, M Peña-Chilet, M Esteban-Medina, ... Frontiers in bioinformatics 3, 1101505, 2023 | | 2023 |
| NPTX1 mutations cause a novel form of autosomal dominant cerebellar ataxia M Coutelier, M Jacoupy, A Janer, F Renaud, G Saripella, F Ancien, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 374-374, 2020 | | 2020 |
| Predicting disease-causing mutation based on their spatial proximity to protein functional sites F Ancien 27th conference on Intelligent Systems for Molecular Biology and 18th …, 2019 | | 2019 |
| Neural network-based predictions of deleterious human variants derived from protein structures and free energy estimations F Ancien, M Godfroid, F Pucci, M Rooman 15th European Conference on Computational Biology, 2016 | | 2016 |
| Supplementary Materials: In silico analysis of the molecular-level impact of SMPD1 variants on Niemann-Pick disease severity. F Ancien, F Pucci, M Rooman | | |
