Author

Bahareh A. Mojarad

Hospital for Sick ChildrenORCID 0000-0003-1943-9163Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anne S. BassettiD· 2 shared Christian R. MarshalliD· 2 shared Giovanna PellecchiaiD· 2 shared Ryan K. C. YueniD· 2 shared Stephen W. SchereriD· 2 shared Tracy HeungiD· 2 shared Worrawat EngchuaniD· 2 shared Aleksandra MitinaiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anne S. BassettORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineMolecular PsychiatryPeer-reviewedMay 11, 2022

Genome-wide tandem repeat expansions contribute to schizophrenia risk

Bahareh A. Mojarad, Worrawat Engchuan, Brett Trost…·Ryan K. C. Yuen

The paper identifies genome-wide rare tandem repeat expansions associated with schizophrenia risk by comparing cases and controls.

46 citationstop 2%

humanwhole-genome sequencing

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GenomicsFrontiers in GeneticsPeer-reviewedSep 15, 2020

Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences

Roozbeh Manshaei, Daniele Merico, Miriam S. Reuter…·Anne S. Bassett

This paper identifies ultra-rare variants in NOTCH1 and FLT4 associated with tetralogy of Fallot using burden analysis of genome sequences from 231 individuals.

36 citations

humanwhole-exome sequencing

𝕏 PostBluesky