Author

Arghavan Omidi

Population Health Research Institute

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

Signature Assays, Organisms & Methods

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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

Ann Le· 1 shared Edward Cui· 1 shared Guillaume ParéiD· 1 shared Michael ChongiD· 1 shared Pedrum Mohammadi‐ShemiraniiD· 1 shared Ricky LaliiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

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6 top collaborators · 15 mutual co-author links

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1 shared paperGenetics

Ann Le

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1 paper

Recent·Most cited

Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories

Ricky Lali, Michael Chong, Arghavan Omidi, Pedrum Mohammadi‐Shemirani, Ann Le, Edward Cui, Guillaume Paré

The paper develops a method to create calibrated rare variant genetic risk scores using exome data, showing strong association with coronary artery disease risk.

Nature Communications · Oct 6, 2021Peer-reviewedGenetics