Author

Charalambos Demetriou

University College LondonORCID 0000-0001-6630-1322Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Gudrun E. MooreiD· 2 shared Miho IshidaiD· 2 shared Andrew M. PrenticeiD· 1 shared Caroline H. D. FalliD· 1 shared Claire WalshiD· 1 shared Constance MaureriD· 1 shared Cristina Alemán-Charlet· 1 shared Dagan JenkinsiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Gudrun E. MooreORCID

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2 papers

Recent·Most cited

GenomicsNucleic Acids ResearchPeer-reviewedJun 17, 2022

Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo

Maria Derakhshan, Noah J. Kessler, Miho Ishida…·Matt J. Silver

The paper identifies hypervariable DNA methylation sites across multiple tissues and ethnicities, showing they are influenced by environmental factors and established early in human development.

15 citations

humanDNA methylation

𝕏 PostBluesky

Developmental BiologyScientific ReportsPeer-reviewedAug 13, 2020

Diverse Species-Specific Phenotypic Consequences of Loss of Function Sorting Nexin 14 Mutations

Dale Bryant, Marian Seda, Emma Peskett…·Philip Stanier

This study examines the phenotypic effects of SNX14 loss-of-function mutations in mice and zebrafish, revealing species-specific consequences despite conserved biochemical roles.

13 citations

mousezebrafish

𝕏 PostBluesky