Author

Adrianna M. Bielowka

NIHR Imperial Biomedical Research CentreORCID 0000-0002-8252-833XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Assay:bulk RNA-seq· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Claire L. ShovliniD· 2 shared Dilip Patel· 2 shared Dongyang LiiD· 2 shared María E Bernabeu-Herrero· 2 shared Micheala A. AldrediD· 2 shared Amy L. RobertsiD· 1 shared Andrew David MumfordiD· 1 shared Awatif Abdulmogith· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersMolecular Biology

Claire L. ShovlinORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Molecular BiologybioRxivPreprintSep 21, 2023

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…·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.

DOI 10.1101/2023.09.21.558767

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintMay 10, 2023

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…·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.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsHuman Molecular GeneticsPeer-reviewedFeb 17, 2020

Genome-wide genetic risk for SLE and disease severity

Lingyan Chen, Yongfei Wang, Lu Liu…·David Lester Morris

This study evaluates genetic risk scores for predicting SLE susceptibility and severity using GWAS data from European and Chinese populations, finding moderate predictive performance and associations with renal disease and age of onset.

102 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky