Author

Philip Tombleson

King's College London

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

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:GWAS summary statistics· 1 Assay:proteomics· 1 Research Focus:variant calling· 1

Frequent Co-Authors

David Lester MorrisiD· 2 shared Timothy James VyseiD· 2 shared Amy L. RobertsiD· 1 shared Ann-Christine Syvänen· 1 shared Aswin SekariD· 1 shared Carl D. LangefeldiD· 1 shared Carlos N. PatoiD· 1 shared Christine E. SeidmaniD· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetics

David Lester MorrisORCID

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2 papers

Recent·Most cited

Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

Nolan Kamitaki, Aswin Sekar, Robert E. Handsaker, Heather de Rivera, Katherine Tooley, David Lester Morris, Kimberly E. Taylor, Christopher W. Whelan, Philip Tombleson, Loes M. Olde Loohuis, Michael Boehnke, Robert P. Kimberly, Kenneth M. Kaufman, John B. Harley, Carl D. Langefeld, , Steven A. McCarroll

This study identifies C4 genes in the MHC locus as sex-specific contributors to risk for lupus, Sjogrens syndrome, and schizophrenia, with stronger effects in men than women.

bioRxiv · Sep 9, 2019 · PreprintGenetics

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