Author

Brendan Kenna

University Medical Center UtrechtORCID 0000-0001-7591-2221Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Approach:machine learning (classical)· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Jan Herman VeldinkiD· 2 shared Johnathan Cooper‐KnockiD· 2 shared Kevin Patrick KennaiD· 2 shared Leonard H. van den BergiD· 2 shared Ahmad Al KhleifatiD· 1 shared Alfredo IacoangeliiD· 1 shared Allan F. McRaeiD· 1 shared Ammar Al‐ChalabiiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Jan Herman VeldinkORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintNov 22, 2024

Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis

Olivia A. Grant, Alfredo Iacoangeli, Ramona A.J. Zwamborn…·Ahmad Al Khleifat

The paper identifies sex-associated DNA methylation differences in ALS using a large-scale epigenome-wide association study and links them to survival outcomes.

4 citations

humanDNA methylation

𝕏 PostBluesky

BioinformaticsbioRxivPreprintMay 30, 2023

Functional clustering of splice-altering variants in whole genome sequencing data reveals hidden heritability in rare variant disorder

Yan Wang, Charlotte van Dijk, Ilia Sarah Timpanaro…·Kevin Patrick Kenna

SpliPath identifies pathogenic splice-altering variants in ALS by integrating SpliceAI predictions with transcriptomics data, revealing hidden heritability in rare variant disorders.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky