Author

Margaret E. Scollan

Regeneron (United States)ORCID 0000-0002-6706-9446Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abby E. Hare-HarrisiD· 1 shared Alan R. ShuldineriD· 1 shared Alexander E. LopeziD· 1 shared Alicia C. Hawes· 1 shared Andrés Moreno-De-LucaiD· 1 shared Aris BarasiD· 1 shared Aris N. EconomidesiD· 1 shared Christa Lese MartiniD· 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 paperGenomics

Abby E. Hare-HarrisORCID

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1 paper

Recent·Most cited

Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes

Evan K. Maxwell, Jonathan S. Packer, Colm T. O’Dushlaine, Shane McCarthy, Abby E. Hare-Harris, Jeffrey C. Staples, Claudia G. Gonzaga-Jauregui, Samantha N. Fetterolf, W. Andrew Faucett, Joseph B. Leader, Andrés Moreno-De-Luca, Giusy Della Gatta, Margaret E. Scollan, Trikaldarshi Persaud, John Penn, , Jeffrey G. Reid

The paper identifies and analyzes exonic copy number variants (CNVs) in 50,726 DiscovEHR participants, linking them to clinical traits and phenotypes.

bioRxiv · Mar 22, 2017 · PreprintGenomics