Lambert Moyon

发表

Classification of non-coding variants with high pathogenic impact.

H. Roest Crollius, Camille Berthelot, A. Louis, 2022, PLoS genetics.

Functional Predictors of Causative Cis-Regulatory Mutations in Mendelian Disease

D. Grozeva, P. Kind, H. R. Crollius, 2020, bioRxiv.

Network Embedding Across Multiple Tissues and Data Modalities Elucidates the Context of Host Factors Important for COVID-19 Infection

Ghalia Rehawi, F. Bittner, A. Marsico, 2022, Frontiers in Genetics.

Towards in silico CLIP-seq: predicting protein-RNA interaction via sequence-to-signal learning

J. Ule, J. Gagneur, O. Winther, 2022, bioRxiv.

Screening for eukaryotic motifs in Legionella pneumophila reveals Smh1 as bacterial deacetylase of host histones

U. Völker, A. Becker, B. Schmeck, 2022, Virulence.

Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability

D. Grozeva, P. Kind, J. Prendergast, 2021, PloS one.

Classification of non-coding variants with high pathogenic impact

H. R. Crollius, Camille Berthelot, A. Louis, 2021, bioRxiv.

A systematic benchmark of machine learning methods for protein–RNA interaction prediction

A. Marsico, Lambert Moyon, Marc Horlacher, 2023, bioRxiv.

Computational Mapping of the Human-SARS-CoV-2 Protein-RNA Interactome

U. Ohler, F. Bittner, A. Marsico, 2021, bioRxiv.

A computational map of the human-SARS-CoV-2 protein–RNA interactome predicted at single-nucleotide resolution

U. Ohler, A. Marsico, Mahsa Ghanbari, 2023, NAR genomics and bioinformatics.

SND1 binds SARS-CoV-2 negative-sense RNA and promotes viral RNA synthesis through NSP9

Mathias Munschauer, Florian Erhard, Steve Carr, 2023, Cell.

Edinburgh Research Explorer Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability

D. Grozeva, O. Spasic-Boskovic, Shipra Bhatia, 2022 .