Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Independent somatic TP53 mutations in blood and tumor mimicking Li-Fraumeni syndrome in a 94-year-old man.
Journal: NPJ precision oncology
Published: December 09, 2025
Breast carcinomas associated with microglandular adenosis are linked to germline alterations in homologous recombination-deficiency genes.
Journal: Research square
Published: June 30, 2025
Breast carcinomas associated with microglandular adenosis are linked to germline alterations in homologous recombination-deficiency genes.
Journal: NPJ breast cancer
Published: May 16, 2025
Genomic Profiling Reveals Germline Predisposition and Homologous Recombination Deficiency in Pancreatic Acinar Cell Carcinoma.
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: August 22, 2023
Recommendations for Cell-Free DNA Assay Validations: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.
Journal: The Journal of molecular diagnostics : JMD
Published: May 03, 2023
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Journal: Nucleic acids research
Published: September 01, 2022
A community approach to the cancer-variant-interpretation bottleneck.
Journal: Nature cancer
Published: May 27, 2022
Comprehensive assessment of germline pathogenic variant detection in tumor-only sequencing.
Journal: Annals of oncology : official journal of the European Society for Medical Oncology
Published: August 04, 2021
Twists and turns from "tumor in tumor" profiling: surveillance of chronic lymphocytic leukemia (CLL) leads to detection of a lung adenocarcinoma, whose genomic characterization alters the original hematologic diagnosis.
Journal: Cold Spring Harbor molecular case studies
Published: February 22, 2021
A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41-q42 deletion phenotype.
Journal: American journal of medical genetics. Part A
Published: October 13, 2017
Showing 1-11 of 11
Last Updated: 09/26/2026