Author

Andrew D. Devereau

Genomics EnglandORCID 0000-0003-0356-1519Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genomics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Assay:CRISPR screen· 1

Frequent Co-Authors

Angela D. HambliniD· 3 shared Christine PatchiD· 3 shared Christopher R. BoustrediD· 3 shared D. Perez-Gil· 3 shared Dalia KasperavičiūtėiD· 3 shared Damian P. SmedleyiD· 3 shared Dimitris PolychronopoulosiD· 3 shared Dina Halai· 3 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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

3 shared papersGenomics

Angela D. HamblinORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedMar 14, 2022

Whole genome sequencing delineates regulatory and novel genic variants in childhood cardiomyopathy

Robert Lesurf, Abdelrahman Said, Oyediran Akinrinade…·R. Sultana

This study uses whole-genome sequencing to identify regulatory and novel genic variants contributing to childhood cardiomyopathy.

46 citationstop 2%

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsNature CancerPeer-reviewedApr 26, 2021

Dissecting mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage

Xueqing Zou, Ching Chiek Koh, Arjun Scott Nanda…·Magdalena Zarowiecki

The paper identifies gene-specific mutational signatures caused by replication errors and endogenous DNA damage using CRISPR-Cas9 knockouts and whole-genome sequencing.

160 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsNature CommunicationsPeer-reviewedJan 31, 2020

Human and mouse essentiality screens as a resource for disease gene discovery

Pilar Cacheiro, Violeta Muñoz‐Fuentes, Stephen A. Murray…·A. Siddiq

The paper integrates gene essentiality data from human and mouse screens to classify genes into FUSIL categories, identifying developmental lethal genes associated with rare diseases.

105 citationstop 2%

𝕏 PostBluesky