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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 19, 2023
Characterization of POT1 tumor predisposition syndrome: Tumor prevalence in a clinically diverse hereditary cancer cohortJennifer Herrera-Mullar, Kelly Fulk, Terra Brannan, et al.Genes|November 27, 2025
A Plot Twist: When RNA Yields Unexpected Findings in Paired DNA-RNA Germline Genetic TestingHeather Zimmermann, Terra Brannan, Colin Young, et al.Familial Cancer|August 4, 2023
Combining clinical and molecular characterization of CDH1: a multidisciplinary approach to reclassification of a splicing variantCorrine Fillman, Arravinth Anantharajah, Briana Marmelstein, et al.Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Saturation genome editing of BARD1 resolves VUS and provides insight into BRCA1-BARD1 tumor suppressionIvan Woo, Silvia Casadei, Matthew W Snyder, et al.Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variantsMarcy E Richardson, Megan Holdren, Terra Brannan, et al.American Journal of Human Genetics|September 24, 2024
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variantsMarcy E Richardson, Megan Holdren, Terra Brannan, et al.American Journal of Human Genetics|September 18, 2025
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variantsMarcy E Richardson, Megan F H Bishop, Megan A Holdren, et al.Journal of Medical Genetics|January 5, 2023
Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelinesXi Luo, Jamie L Maciaszek, Bryony A Thompson, et al.Pageof 1