Author

Terra Brannan

Ambry Genetics (United States)

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· 3

Signature Assays, Organisms & Methods

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Research Focus:database / resource· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amanda B. SpurdleiD· 2 shared Marcy E. RichardsoniD· 2 shared Tina F. PesaraniD· 2 shared Abbye E. McEweniD· 1 shared Airi HosokaiiD· 1 shared Alicia XuiD· 1 shared Álvaro N.A. MonteiroiD· 1 shared Arjen R. MensenkampiD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Amanda B. SpurdleORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Saturation genome editing of BARD1 resolves VUS and provides insight into BRCA1-BARD1 tumor suppression

Ivan M. H. Woo, Silvia Casadei, Matthew W. Snyder, Nahum T. Smith, Sabrina Best, Malvika Tejura, Pankhuri Gupta, Abbye E. McEwen, Mason Post, Audrey Hamm, Moez Dawood, Airi Hosokai, Alicia Xu, Riddhiman K. Garge, Shawn Fayer, , Lea M. Starita

The paper uses saturation genome editing to evaluate BARD1 variants, resolving most variants of uncertain significance and confirming their role in tumor suppression.

medRxiv · Nov 3, 2025 · PreprintGenetic & Genomic Medicine

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants

Marcy E. Richardson, Megan A. Holdren, Terra Brannan, Miguel de la Hoya, Amanda B. Spurdle, Sean V. Tavtigian, Colin C. Young, Lauren Zec, Susan C. Hiraki, Michael J. Anderson, Logan C. Walker, Shannon M. McNulty, Clare Turnbull, Marc D. Tischkowitz, Katherine R. Schon, , Fergus J. Couch

The paper specifies gene-specific rules for interpreting ATM variants using ACMG/AMP guidelines, improving classification accuracy in a pilot study.

medRxiv · May 28, 2024 · PreprintGenetic & Genomic Medicine

ClinGen CDH1 specifications for the ACMG/AMP guidelines: improvement of germline variant clinical assertions and updated curation guidelines

Xi Luo, Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E. Roberts, Kristy Lee, Amanda B. Spurdle, Arjen R. Mensenkamp, Terra Brannan, Carolina Pardo, Liying Zhang, Tina F. Pesaran, , Rachid Karam

The paper updates CDH1 variant curation guidelines to resolve conflicting interpretations and reduce variants of uncertain significance for clinical use.

medRxiv · Nov 1, 2021 · PreprintGenetic & Genomic Medicine