Author

Cheryl A. Roe

SUNY Upstate Medical University

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

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Genetics· 1

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ashley Dumont· 1 shared Benjamin M. NealeiD· 1 shared Claire L. ChurchhouseiD· 1 shared Daniel P. HowriganiD· 1 shared Felecia E. CerratoiD· 1 shared Giulio GenoveseiD· 1 shared Hai‐Gwo HwuiD· 1 shared Jack A. KosmickiiD· 1 shared

Activity by Year

2018-2018 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Ashley Dumont

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1 paper

Recent·Most cited

Schizophrenia risk conferred by protein-coding de novo mutations

Daniel P. Howrigan, Samuel A. Rose, Kaitlin E. Samocha, Menachem Fromer, Felecia E. Cerrato, Wei J. Chen, Claire L. Churchhouse, Kimberly Chambert, Sharon D. Chandler, Mark J. Daly, Ashley Dumont, Giulio Genovese, Hai‐Gwo Hwu, Nan M. Laird, Jack A. Kosmicki, , Benjamin M. Neale

This study examines the contribution of protein-coding de novo mutations to schizophrenia risk using whole-exome sequencing data from parent-offspring trios, finding a modest but polygenic effect.

bioRxiv · Dec 13, 2018 · PreprintGenetics