Author

Dylan Aïssi

Universität HamburgORCID 0000-0002-5858-6468Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 2 Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:eQTL / molecular QTL mapping· 2 Research Focus:software / tool· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Research Focus:fine-mapping· 1

Frequent Co-Authors

Jean‐François DeleuzeiD· 2 shared Marine GermainiD· 2 shared Pierre‐Emmanuel MorangeiD· 2 shared Robert OlasoiD· 2 shared Ahmad Al KhleifatiD· 1 shared Aleksey ShatunoviD· 1 shared Alex P. ReineriD· 1 shared Alexia CardonaiD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jean‐François DeleuzeORCID

Mutual co-authors in cluster

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4 papers

Recent·Most cited

Genetic & Genomic MedicineCirculationPeer-reviewedOct 17, 2022

Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

Florian Thibord, Derek M. Klarin, Jennifer A. Brody…·Nicholas L. Smith

This study identifies 135 genomic loci associated with venous thromboembolism risk through cross-ancestry GWAS and provides insights into biological pathways and potential therapeutic targets.

105 citationstop 1%

humanGWAS summary statistics

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Genetic & Genomic MedicineNature GeneticsPeer-reviewedSep 1, 2021

Genomic and phenomic insights from an atlas of genetic effects on DNA methylation

Josine L. Min, Gibran Hemani, Eilis J. Hannon…·Marinus H. van IJzendoorn

The paper identifies genetic variants influencing DNA methylation in blood and shows their associations with complex traits and diseases, but finds limited direct causality.

508 citationstop 1%

humanDNA methylation

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BioinformaticsbioRxivPreprintMar 29, 2020

MORFEE: a new tool for detecting and annotating single nucleotide variants creating premature ATG codons from VCF files

Dylan Aïssi, Omar Soukarieh, Carole Proust…·David‐Alexandre Trégouët

MORFEE identifies and annotates single nucleotide variants in 5UTR regions that create upstream open reading frames (uORFs) from VCF files, aiding in interpreting genetic association signals and disease mechanisms.

9 citations

humanwhole-genome sequencing

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BioinformaticsBMC BioinformaticsPeer-reviewedAug 22, 2018

bioSyntax: Syntax Highlighting For Computational Biology

Artem Babaian, Anicet Ebou, Alyssa Fegen…·Yao Li

bioSyntax provides syntax highlighting tools for computational biology data formats to improve readability and efficiency.

5 citations

software / tool

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