Author

Bridget Carter

Emory University

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

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alba Sanchis‐JuaniD· 1 shared Claudia RestrepoiD· 1 shared David J. CutleriD· 1 shared Eleanor FeingoldiD· 1 shared Elizabeth J. LeslieiD· 1 shared George L. WehbyiD· 1 shared Harrison BrandiD· 1 shared Jacqueline T. HechtiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alba Sanchis‐JuanORCID

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1 paper

Recent·Most cited

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

Kimberly K. Diaz Perez, Sarah W. Curtis, Alba Sanchis‐Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho, Bridget Carter, Toby Goldstein McHenry, Madison R. Bishop, Luz Consuelo Valencia‐Ramirez, Claudia Restrepo, Jacqueline T. Hecht, Lina M. Moreno Uribe, George L. Wehby, Seth Michael Weinberg, , Elizabeth J. Leslie

The paper estimates the diagnostic yield of sequencing 418 genes in OFC cases and controls, finding a higher prevalence of likely pathogenic variants in cases.

Genetics in Medicine · Jun 15, 2023Peer-reviewedGenetic & Genomic Medicine