Author

Raissa Relator

London Health Sciences CentreORCID 0000-0002-8153-2222Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Assay:DNA methylation· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Bekim SadikovićiD· 2 shared Haley McConkey· 2 shared Michael A. LevyiD· 2 shared Abu SaadatiD· 1 shared Amy SchneideriD· 1 shared Andrea RiccioiD· 1 shared Angela SparagoiD· 1 shared Ankit VermaiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetics

Bekim SadikovićORCID

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2 papers

Recent·Most cited

Identification of genetic and non-genetic modifiers of genomic imprinting through whole genome screening in humans

Francesco Cecere, Raissa Relator, Michael A. Levy, Ankit Verma, Haley McConkey, Bruno Hay Mele, Laura Pignata, Carlo Giaccari, Emilia D’Angelo, Subham Saha, Abu Saadat, Angela Sparago, Claudia Angelini, Flavia Cerrato, Bekim Sadiković, Andrea Riccio

The paper identifies genetic and non-genetic factors influencing genomic imprinting by analyzing methylation patterns in iDMRs across a large cohort of individuals.

bioRxiv · Mar 27, 2025 · PreprintGenetics

Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature

Christy W. LaFlamme, Cassandra Rastin, Soham Sengupta, Helen E. Pennington, Sophie J. Russ-Hall, Amy Schneider, Emily S. Bonkowski, Edith P. Almanza Fuerte, Talia J. Allan, Miranda Galey, Joy Goffena, Sophia B Gibson, Denis M. Nyaga, Nico Lieffering, Malavika Hebbar, , Heather C. Mefford

This study evaluates genome-wide DNA methylation analysis in genetically unsolved DEEs, identifying 10 causative or candidate genetic causes and refining a CHD2 episignature.

Nature Communications · Aug 6, 2024Peer-reviewedGenetic & Genomic Medicine