Author

Simon Vyse

King's College LondonORCID 0000-0002-0582-2869Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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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

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1 shared paperGenetics

Amy L. RobertsORCID

Mutual co-authors in cluster

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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