Author

Tracy Heung

University Health NetworkORCID 0000-0003-1860-7292Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anne S. BassettiD· 3 shared Bahareh A. MojaradiD· 2 shared Christian R. MarshalliD· 2 shared Giovanna PellecchiaiD· 2 shared Ryan K. C. YueniD· 2 shared Stephen W. SchereriD· 2 shared Worrawat EngchuaniD· 2 shared Aleksandra MitinaiD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersGenetics

Anne S. BassettORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintMar 14, 2024

Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome

Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos…·Joris Robert Vermeesch

The paper investigates the mechanisms behind the high incidence of 22q11.2 deletion syndrome by analyzing recombination events and paralogous structures in LCR22 regions.

DOI 10.1101/2024.03.14.585046

humanwhole-genome sequencing

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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