Author

Christine Stevens

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:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Daniel Graham· 2 shared NIDDK IBD Genetics consortium· 2 shared Aarno Palotie· 1 shared Adam P. Levine· 1 shared Andre Franke· 1 shared Andrea Ganna· 1 shared Ann Pulver· 1 shared Anthony W. Segal· 1 shared

Activity by Year

2016-2016 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenetics

Daniel Graham

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2 papers

Recent·Most cited

Insights into the genetic epidemiology of Crohn’s and rare diseases in the Ashkenazi Jewish population

Manuel A. Rivas, Jukka Koskela, Hailiang Huang, Christine Stevens, Brandon E. Avila, Talin Haritunians, Benjamin M. Neale, Mitja Kurki, Andrea Ganna, Daniel Graham, Benjamin Glaser, Inga Peter, Gil Atzmon, Nir Barzilai, Adam P. Levine, , Mark J. Daly

The paper analyzes exome sequencing data from Ashkenazi Jews to identify enriched alleles and their association with genetic risk for Crohn’s disease and rare diseases.

bioRxiv · Sep 25, 2016 · PreprintGenetics

A protein truncating R179X variant in RNF186 confers protection against ulcerative colitis

Manuel A Rivas, Daniel Graham, Patrick Sulem, Christine Stevens, Nicole Desch, Philippe Goyette, Daniel Gudbjartsson, Ingileif Jonsdottir, Unnur Thorsteinsdottir, Frauke Degenhardt, Soren Mucha, Mitja I Kurki, Dalin Li, Mauro D'Amato, Vito Annese, , Steve

The paper identifies a protein truncating variant in RNF186 that protects against ulcerative colitis by reducing disease risk.

Nature Communications · Aug 9, 2016Peer-reviewedGenetics