Author

Mishan Britto

University of Warwick

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Benjamin Heath DurhamiD· 1 shared Margaret T. Lee· 1 shared Masanori MishimaiD· 1 shared Sandeep N. WontakaliD· 1 shared Sarah Tannenbaum· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

5 top collaborators · 10 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

Benjamin Heath DurhamORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 7, 2021

A rare congenital anemia is caused by mutations in the centralspindlin complex

Sandeep N. Wontakal, Mishan Britto, Sarah Tannenbaum…·Masanori Mishima

This study identifies compound heterozygous RACGAP1 variants causing CDAIII by disrupting the centralspindlin complex, leading to cytokinesis defects.

DOI 10.1101/2021.04.07.21254990

humanexperimental assay

𝕏 PostBluesky