Author

Candice K. Silversides

University Health Network

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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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Anne S. BassettiD· 2 shared Christian R. MarshalliD· 2 shared Giovanna PellecchiaiD· 2 shared Miriam S. ReuteriD· 2 shared Rachel Maya WaldiD· 2 shared Rajiv R ChaturvediiD· 2 shared Rebekah JoblingiD· 2 shared Stephen W. SchereriD· 2 shared

Activity by Year

2020-2021 · 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

Clinical genetic risk variants inform a functional protein interaction network for tetralogy of Fallot

Miriam S. Reuter, Rajiv R Chaturvedi, Rebekah Jobling, Giovanna Pellecchia, Omar Hamdan, Wilson W. L. Sung, Thomas Nalpathamkalam, Pratyusha Attaluri, Candice K. Silversides, Rachel Maya Wald, Christian R. Marshall, Simon G. Williams, Bernard D. Keavney, Bhooma Thiruvahindrapuram, Stephen W. Scherer, Anne S. Bassett

The paper identifies clinically relevant genetic variants in TOF patients and constructs a protein interaction network linking these variants to disease mechanisms.

Circulation Genomic and Precision Medicine · Jul 30, 2021Peer-reviewedGenetic & Genomic Medicine

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, Worrawat Engchuan, Bahareh A. Mojarad, Rajiv R Chaturvedi, Tracy Heung, Giovanna Pellecchia, Mehdi Zarrei, Thomas Nalpathamkalam, Reem Khan, John B. A. Okello, Eriskay Liston, Meredith Curtis, Ryan K. C. Yuen, , 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.

Frontiers in Genetics · Sep 15, 2020Peer-reviewedGenomics