Frederic Rousseau
Affiliations:- KU Leuven, Department of Cellular and Molecular Medicine, Belgium
According to our database1,
Frederic Rousseau
authored at least 28 papers
between 2005 and 2023.
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Bibliography
2023
SNPeffect 5.0: large-scale structural phenotyping of protein coding variants extracted from next-generation sequencing data using AlphaFold models.
BMC Bioinform., December, 2023
2021
In silico prediction of in vitro protein liquid-liquid phase separation experiments outcomes with multi-head neural attention.
Bioinform., 2021
2020
WALTZ-DB 2.0: an updated database containing structural information of experimentally determined amyloid-forming peptides.
Nucleic Acids Res., 2020
2019
Bioinform., 2019
2016
From Binding-Induced Dynamic Effects in SH3 Structures to Evolutionary Conserved Sectors.
PLoS Comput. Biol., 2016
2015
Increased Aggregation Is More Frequently Associated to Human Disease-Associated Mutations Than to Neutral Polymorphisms.
PLoS Comput. Biol., 2015
PrionW: a server to identify proteins containing glutamine/asparagine rich prion-like domains and their amyloid cores.
Nucleic Acids Res., 2015
2013
Motif Discovery with Data Mining in 3D protein Structure Databases: Discovery, Validation and Prediction of the U-Shape zinc binding ("Huf-zinc") Motif.
J. Bioinform. Comput. Biol., 2013
2012
SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.
Nucleic Acids Res., 2012
2011
An Evolutionary Trade-Off between Protein Turnover Rate and Protein Aggregation Favors a Higher Aggregation Propensity in Fast Degrading Proteins.
PLoS Comput. Biol., 2011
BriX: a database of protein building blocks for structural analysis, modeling and design.
Nucleic Acids Res., 2011
2010
Nucleic Acids Res., 2010
BMC Bioinform., 2010
2009
Accurate Prediction of DnaK-Peptide Binding via Homology Modelling and Experimental Data.
PLoS Comput. Biol., 2009
BMC Syst. Biol., 2009
Using structural bioinformatics to investigate the impact of non synonymous SNPs and disease mutations: scope and limitations.
BMC Bioinform., 2009
2008
Genome-Wide Prediction of SH2 Domain Targets Using Structural Information and the FoldX Algorithm.
PLoS Comput. Biol., 2008
Reconstruction of Protein Backbones from the BriX Collection of Canonical Protein Fragments.
PLoS Comput. Biol., 2008
Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases.
Nucleic Acids Res., 2008
2006
PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes.
Nucleic Acids Res., 2006
SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.
Bioinform., 2006
2005
SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs.
Nucleic Acids Res., 2005