Author

Margarita Rivera

King's College LondonORCID 0000-0003-4717-1045Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:eQTL / molecular QTL mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Carlos N. PatoiD· 2 shared A. M. McIntoshiD· 1 shared Adam E. LockeiD· 1 shared Aiden Peter CorviniD· 1 shared Alessandro BertolinoiD· 1 shared Alessandro SerrettiiD· 1 shared Alice BrauniD· 1 shared Andrew McQuilliniD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenomics

Carlos N. PatoORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

GenomicsbioRxivPreprintFeb 11, 2026

Co-expression-based models improve eQTL predictions and highlightnovel transcriptome-wide genes associated with schizophrenia

Fabiana Rossi, Leonardo Sportelli, Gianluca Christos Kikidis…·Giulio Pergola

The paper introduces co-expression-based models to improve eQTL predictions and identifies novel schizophrenia-associated genes using brain RNA-seq data.

DOI 10.64898/2026.02.10.704353

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsNature CommunicationsPeer-reviewedSep 10, 2018

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

Jedidiah Carlson, Adam E. Locke, Matthew Flickinger…·Stanley J. Watson

The paper analyzes rare variants to uncover mutation rate heterogeneity in the human genome, identifying genomic features that influence mutation rates.

132 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky