Author

Dilip Patel

NIHR Imperial Biomedical Research Centre

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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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adrianna M. BielowkaiD· 2 shared Claire L. ShovliniD· 2 shared Dongyang LiiD· 2 shared María E Bernabeu-Herrero· 2 shared Micheala A. AldrediD· 2 shared Andrew David MumfordiD· 1 shared Awatif Abdulmogith· 1 shared Dan MurphyiD· 1 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersMolecular Biology

Adrianna M. BielowkaORCID

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2 papers

Recent·Most cited

Transcriptome-wide analysis of primary human endothelial cell responses to 1 hour of protein translation inhibition identify nonsense mediated decay targets and a non-coding SLC11A2 exon as an acute biomarker

Adrianna M. Bielowka, Fatima S Govani, Dilip Patel, María E Bernabeu-Herrero, Dongyang Li, Micheala A. Aldred, Inês G. Mollet, Claire L. Shovlin

The paper identifies NMD targets and a non-coding SLC11A2 exon as an acute biomarker by analyzing transcriptome changes in human endothelial cells after cycloheximide treatment.

bioRxiv · Sep 21, 2023 · PreprintMolecular Biology

Functional filter for whole genome sequence data identifies stress impact, non-coding, alternate polyadenylation site variants >5kb from coding DNA

Sihao Xiao, Zhentian Kai, Dan Murphy, Dongyang Li, Dilip Patel, Adrianna M. Bielowka, María E Bernabeu-Herrero, Awatif Abdulmogith, Andrew David Mumford, Sarah K. Westbury, Micheala A. Aldred, Neil Vargesson, Mark J. Caulfield, Claire L. Shovlin

GROFFFY filters whole genome sequence data to identify non-coding and polyadenylation site variants, improving detection of disease-causing variants in unsolved cases.

medRxiv · May 10, 2023 · PreprintGenetic & Genomic Medicine