Author

Venu Pullabhatla

Guy's and St Thomas' NHS Foundation Trust

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

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amy L. RobertsiD· 1 shared Ann-Christine Syvänen· 1 shared Christopher A. OdhamsiD· 1 shared Daniele MauroiD· 1 shared David Lester MorrisiD· 1 shared Emanuele de RinaldisiD· 1 shared Michael A. SimpsoniD· 1 shared Myles LewisiD· 1 shared

Activity by Year

2017-2017 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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 paperGenetics

Amy L. RobertsORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

De Novo Mutations Implicate Novel Genes With Burden Of Rare Variants In Systemic Lupus Erythematosus

Venu Pullabhatla, Amy L. Roberts, Myles Lewis, Daniele Mauro, David Lester Morris, Christopher A. Odhams, Philip Tombleson, Ulrika Liljedahl, Simon Vyse, Michael A. Simpson, Sascha Sauer, Emanuele de Rinaldis, Ann-Christine Syvänen, Timothy James Vyse

This study identifies de novo mutations and rare variant burdens in SLE candidate genes, supporting their role in disease pathogenesis.

Human Molecular Genetics · Nov 20, 2017Peer-reviewedGenetics