Author

Carolyn Erdman

University of California, San Francisco

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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Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. Jeremy Willsey· 1 shared Aaron R. QuinlaniD· 1 shared Andrew FarrelliD· 1 shared Arnold R. KriegsteiniD· 1 shared Benjamin CurralliD· 1 shared Benjamin M. NealeiD· 1 shared Bernie DevliniD· 1 shared Buxbaum Jn· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

A. Jeremy Willsey

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1 paper

Recent·Most cited

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

Donna M. Werling, Harrison Brand, Joon‐Yong An, Matthew R. Stone, Joseph Glessner, Lingxue Zhu, Ryan L. Collins, Shan Dong, Ryan M. Layer, Eirene Markenscoff-Papadimitriou, Andrew Farrell, Grace Schwartz, Benjamin Currall, Jeanselle Dea, Clif Duhn, , Stephan Sanders

This study examines the role of noncoding variation in autism spectrum disorder using whole genome sequencing of 2,076 genomes, finding no significant association after correction for multiple testing.

European Neuropsychopharmacology · Jan 1, 2019Peer-reviewedGenomics