Author

Sarah Wolf

Regeneron (United States)Primary ORCID profile (0009-0006-6308-4434 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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

Same name, identified by ORCID

Sarah WolfiD1 paper · University of Helsinki

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

GenomicsbioRxivPreprintMar 22, 2017

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

Evan K. Maxwell, Jonathan S. Packer, Colm T. O’Dushlaine…·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.

11 citations

humanwhole-exome sequencing

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