Frederic Rousseau

According to our database1, Frederic Rousseau
  • authored at least 25 papers between 2005 and 2015.
  • has a "Dijkstra number"2 of five.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Other 

Links

On csauthors.net:

Bibliography

2015
What Makes a Protein Sequence a Prion?
PLoS Computational Biology, 2015

Increased Aggregation Is More Frequently Associated to Human Disease-Associated Mutations Than to Neutral Polymorphisms.
PLoS Computational Biology, 2015

PrionW: a server to identify proteins containing glutamine/asparagine rich prion-like domains and their amyloid cores.
Nucleic Acids Research, 2015

WALTZ-DB: a benchmark database of amyloidogenic hexapeptides.
Bioinformatics, 2015

Solubis: optimize your protein.
Bioinformatics, 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. Bioinformatics and Computational Biology, 2013

2012
SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.
Nucleic Acids Research, 2012

2011
An Evolutionary Trade-Off between Protein Turnover Rate and Protein Aggregation Favors a Higher Aggregation Propensity in Fast Degrading Proteins.
PLoS Computational Biology, 2011

BriX: a database of protein building blocks for structural analysis, modeling and design.
Nucleic Acids Research, 2011

A graphical interface for the FoldX forcefield.
Bioinformatics, 2011

2010
PepX: a structural database of non-redundant protein-peptide complexes.
Nucleic Acids Research, 2010

Modeling protein-peptide interactions using protein fragments: fitting the pieces?
BMC Bioinformatics, 2010

2009
Accurate Prediction of DnaK-Peptide Binding via Homology Modelling and Experimental Data.
PLoS Computational Biology, 2009

Information theoretical quantification of cooperativity in signalling complexes.
BMC Systems Biology, 2009

Using structural bioinformatics to investigate the impact of non synonymous SNPs and disease mutations: scope and limitations.
BMC Bioinformatics, 2009

2008
Genome-Wide Prediction of SH2 Domain Targets Using Structural Information and the FoldX Algorithm.
PLoS Computational Biology, 2008

Reconstruction of Protein Backbones from the BriX Collection of Canonical Protein Fragments.
PLoS Computational Biology, 2008

Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases.
Nucleic Acids Research, 2008

Using structural bioinformatics to investigate the impact of non synonymous SNPs and disease mutations: scope and limitations.
Proceedings of the ECCB 2008 Workshop: Annotation, 2008

2007
Enhanced Security by OS-Oriented Encapsulation in TPM-Enabled DRM.
Proceedings of the Information Security and Cryptology, Third SKLOIS Conference, 2007

Secure Two-Party Computation of Squared Euclidean Distances in the Presence of Malicious Adversaries.
Proceedings of the Information Security and Cryptology, Third SKLOIS Conference, 2007

2006
PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes.
Nucleic Acids Research, 2006

SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.
Bioinformatics, 2006

2005
The FoldX web server: an online force field.
Nucleic Acids Research, 2005

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs.
Nucleic Acids Research, 2005


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