Author

Amel Haj Khelil

University of MonastirORCID 0000-0001-5404-2116Unclaimed 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:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Ali Neji· 1 shared Amelia Eva AránegaiD· 1 shared Diego FrancoiD· 1 shared Houria DaimiiD· 1 shared Jemni Ben ChibaniiD· 1 shared Khaldoun Ben Hamda· 1 shared Sabri Maaoui· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

7 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Ali Neji

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1 paper

Recent·Most cited

GeneticsBiomedical JournalPeer-reviewedAug 1, 2019

Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What’s behind the scenes?

Houria Daimi, Amel Haj Khelil, Ali Neji…·Diego Franco

The paper identifies genetic variants in SCN5A and its regulatory regions in a Brugada syndrome family, suggesting non-coding variants may contribute to disease through miRNA regulation.

20 citations

humanDNA methylation