Last Updated: 09/26/2026
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Found 14 publications
Ultra-deep duplex sequencing reveals unique features of somatic evolution in the normal tissues of a family with Li-Fraumeni syndrome.
Journal: bioRxiv : the preprint server for biology
Published: February 06, 2026
Long-Term Survival Following Chemoradiation in Locoregional Recurrent Germline ATM Mutated Pancreatic Ductal Adenocarcinoma.
Journal: Advances in radiation oncology
Published: January 17, 2025
Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassifications.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 09, 2025
Lessons learned in migrating from one commercial genetics clinical decision-making tool to another: Assessment of data integrity and utilization.
Journal: Genetics in medicine open
Published: July 22, 2024
Combined Germline and Mosaic SDHA Mutation Is Associated With a Multicancer Syndrome Including Neuroblastoma, Renal Cancer, and Multifocal GI Tumor.
Journal: JCO precision oncology
Published: June 17, 2024
Assessment of a Peer Physician Coaching Partnership Between a Designated Cancer Center Genetics Service and a Community Cancer Network Hospital.
Journal: JAMA network open
Published: March 06, 2023
Genetic Testing Among Patients with High-Risk Breast, Ovarian, Pancreatic, and Prostate Cancers.
Journal: Annals of surgical oncology
Published: August 15, 2022
Multiple Primary Cancers in Patients Undergoing Tumor-Normal Sequencing Define Novel Associations.
Journal: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
Published: July 02, 2021
Inherited TP53 Variants and Risk of Prostate Cancer.
Journal: European urology
Published: May 09, 2021
Last Updated: 09/26/2026