Author

Joan Wilson

National Human Genome Research InstituteORCID 0000-0002-9153-2920Unclaimed ORCID profile · follow to get notified of new preprints

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Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alan F. ScottiD· 1 shared Alexandre BureauiD· 1 shared Ferdouse BegumiD· 1 shared Hasan Albacha‐Hejazi· 1 shared Ingo RuczinskiiD· 1 shared Jacqueline B. HetmanskiiD· 1 shared Jeffrey Clark MurrayiD· 1 shared Margaret A. TaubiD· 1 shared

Activity by Year

2018-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Alan F. ScottORCID

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1 paper

Recent·Most cited

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

Alexandre Bureau, Ferdouse Begum, Margaret A. Taub, Jacqueline B. Hetmanski, Margaret M. Parker, Hasan Albacha‐Hejazi, Alan F. Scott, Jeffrey Clark Murray, Mary L. Marazita, Joan Wilson, Terri H. Beaty, Ingo Ruczinski

This paper extends the Rare Variant Sharing method to handle partial variant sharing in multiplex pedigrees, showing improved power over existing methods in simulations and real data.

Genetic Epidemiology · Sep 24, 2018Peer-reviewedGenetics