Author

Khaldoun Ben Hamda

Hospital Fatuma Bourguiba Monastir

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1

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 Amel Haj KheliliD· 1 shared Amelia Eva AránegaiD· 1 shared Diego FrancoiD· 1 shared Houria DaimiiD· 1 shared Jemni Ben ChibaniiD· 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

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

Houria Daimi, Amel Haj Khelil, Ali Neji, Khaldoun Ben Hamda, Sabri Maaoui, Amelia Eva Aránega, Jemni Ben Chibani, 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.

Biomedical Journal · Aug 1, 2019Peer-reviewedGenetics