Hervé Isambert

Orcid: 0000-0001-9638-8545

According to our database1, Hervé Isambert authored at least 15 papers between 2005 and 2023.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
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Links

On csauthors.net:

Bibliography

2023
Learning interpretable causal networks from very large datasets, application to 400, 000 medical records of breast cancer patients.
CoRR, 2023

2022
Interactive exploration of a global clinical network from a large breast cancer cohort.
npj Digit. Medicine, 2022

2021
NeuriTES. Monitoring neurite changes through transfer entropy and semantic segmentation in bright-field time-lapse microscopy.
Patterns, 2021

2020
Learning clinical networks from medical records based on information estimates in mixed-type data.
PLoS Comput. Biol., 2020

OHNOLOGS v2: a comprehensive resource for the genes retained from whole genome duplication in vertebrates.
Nucleic Acids Res., 2020

2019
Constraint-based Causal Structure Learning with Consistent Separating Sets.
Proceedings of the Advances in Neural Information Processing Systems 32: Annual Conference on Neural Information Processing Systems 2019, 2019

2018
MIIC online: a web server to reconstruct causal or non-causal networks from non-perturbative data.
Bioinform., 2018

2017
Learning causal networks with latent variables from multivariate information in genomic data.
PLoS Comput. Biol., 2017

2016
3off2: A network reconstruction algorithm based on 2-point and 3-point information statistics.
BMC Bioinform., 2016

2015
Identification of Ohnolog Genes Originating from Whole Genome Duplication in Early Vertebrates, Based on Synteny Comparison across Multiple Genomes.
PLoS Comput. Biol., 2015

Robust Reconstruction of Causal Graphical Models based on Conditional 2-point and 3-point Information.
Proceedings of the UAI 2015 Workshop on Advances in Causal Inference co-located with the 31st Conference on Uncertainty in Artificial Intelligence (UAI 2015), 2015

2014
Human Dominant Disease Genes Are Enriched in Paralogs Originating from Whole Genome Duplication.
PLoS Comput. Biol., 2014

On the expansion of "dangerous" gene families in vertebrates.
BMC Bioinform., 2014

2007
Modeling protein network evolution under genome duplication and domain shuffling.
BMC Syst. Biol., 2007

2005
Kinefold web server for RNA/DNA folding path and structure prediction including pseudoknots and knots.
Nucleic Acids Res., 2005


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