Author

Mwenda R. Rintari

University of ExeterORCID 0009-0005-9908-5669Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alistair T. PagnamentaiD· 1 shared Carolina Jaramillo OquendoiD· 1 shared Caroline Fiona WrightiD· 1 shared Diana BaralleiD· 1 shared Joseph S. LeslieiD· 1 shared V. Kartik ChundruiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 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

1 shared paperGenetic & Genomic Medicine

Alistair T. PagnamentaORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 13, 2026

Investigating the pathogenicity of missense spliceogenic variants using whole-genome sequencing, RNA-sequencing, and proteomics data from population and clinical research cohorts

Mwenda R. Rintari, V. Kartik Chundru, Carolina Jaramillo Oquendo…·Caroline Fiona Wright

The paper investigates missense spliceogenic variants (MSVs) using genomic and proteomic data, finding they are common and can cause disease through splicing disruption, often missed by protein-centric tools.

DOI 10.64898/2026.10.09.26365070

humanwhole-genome sequencing

𝕏 PostBluesky