Author

Quinten Patterson

The University of Texas Southwestern Medical Center

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

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Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Organism:zebrafish· 1

Frequent Co-Authors

Abhijit DixitiD· 1 shared Alex Cash· 1 shared Ana Beleza‐MeirelesiD· 1 shared Athina VerveriiD· 1 shared Caitlin A. ChangiD· 1 shared Christopher HealyiD· 1 shared Denise K. MarcianoiD· 1 shared Diana BaralleiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Abhijit DixitORCID

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1 paper

Recent·Most cited

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Reham Alharatani, Athina Ververi, Ana Beleza‐Meireles, Weizhen Ji, Emily Kathryn Mis, Quinten Patterson, John N. Griffin, Nabina Bhujel, Caitlin A. Chang, Abhijit Dixit, Monica Konstantino, Christopher Healy, Sumayyah Hannan, Natsuko Neo, Alex Cash, , Karen J. Liu

The paper identifies novel truncating mutations in CTNND1 associated with craniofacial and cardiac anomalies, expanding the known phenotypic spectrum of the gene.

Human Molecular Genetics · Mar 17, 2020Peer-reviewedGenetics