Author

Manmeet Virdee

Yale University

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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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abha R. GuptaiD· 1 shared Arthur Jeremy WillseyiD· 1 shared Carolina CappiiD· 1 shared Catherine A.W. SullivaniD· 1 shared Ellen J. HoffmaniD· 1 shared Eurı́pedes Constantino MigueliD· 1 shared Gwyneth C. ZaiiD· 1 shared James L. KennedyiD· 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 paperGenetics

Abha R. GuptaORCID

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1 paper

Recent·Most cited

De novo damaging coding mutations are strongly associated with obsessive-compulsive disorder and overlap with autism

Carolina Cappi, Melody E. Oliphant, Zsanett Péter, Gwyneth C. Zai, Catherine A.W. Sullivan, Abha R. Gupta, Ellen J. Hoffman, Manmeet Virdee, Arthur Jeremy Willsey, Roseli Gedanke Shavitt, Eurı́pedes Constantino Miguel, James L. Kennedy, Margaret Anne Richter, Thomas V. Fernandez

The paper identifies de novo damaging mutations in OCD and finds overlap with autism genes, suggesting shared genetic risk.

bioRxiv · Sep 21, 2017 · PreprintGenetics