Author

Leonidas Salichos

Yale UniversityORCID 0000-0003-0228-6885Unclaimed ORCID profile · follow to get notified of new preprints

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Leonidas Salichos1 paper

Biology Disciplines

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Genomics· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Research Focus:variant effect prediction· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1

Frequent Co-Authors

Shantao LiiD· 3 shared Alexander Martinez‐FundichelyiD· 2 shared Arif O. HarmanciiD· 2 shared Calvin Wing Yiu ChaniD· 2 shared Carl HerrmanniD· 2 shared Ekta KhuranaiD· 2 shared Gad A. GetziD· 2 shared Jakob Skou PederseniD· 2 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Shantao LiORCID

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3 papers

Recent·Most cited

GenomicsCellPeer-reviewedMar 1, 2023

The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models

Joel S. Rozowsky, Jiahao Gao, Beatrice Borsari…·B Bernstein

The paper introduces the EN-TEx resource, which provides personal epigenomes and variant-impact models across multiple tissues, revealing allele-specific loci and their associations with GWAS loci.

78 citationstop 1%

humanDNA methylation

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BioinformaticsNature CommunicationsPeer-reviewedFeb 5, 2020

Integrative pathway enrichment analysis of multivariate omics data

Marta Paczkowska, Jonathan Barenboim, Nardnisa Sintupisut…·Leonidas Salichos

ActivePathways integrates multivariate omics data to identify enriched pathways, revealing cancer driver genes and prognostic pathways in breast cancer.

223 citationstop 1%

humanwhole-genome sequencing

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GenomicsbioRxivPreprintMar 12, 2018

Passenger mutations in 2500 cancer genomes: Overall molecular functional impact and consequences

Sushant Kumar, Jonathan Warrell, Shantao Li…·Mark Gerstein

The paper analyzes 2500 cancer genomes to assess the molecular functional impact of mutations, finding that some putative passenger variants may influence gene activity and contribute to cancer phenotypes.

5 citations

humanwhole-genome sequencing

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