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JCO Precision Oncology|January 7, 2022
Clinical Implications of Pathogenic Germline Variants in Small Intestine Neuroendocrine Tumors (SI-NETs)Kimberly Perez, Matthew H Kulke, Anu Chittenden, et al.
JAMA|June 5, 2023
Germline Genetic Testing After Cancer DiagnosisAllison W Kurian, Paul Abrahamse, Allison Furgal, et al.
Prostate Cancer and Prostatic Diseases|March 1, 2022
Germline alterations among Hispanic men with prostate cancerElizabeth Pan, Justin Shaya, Lisa Madlensky, et al.
Epilepsia Open|August 24, 2019
Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsyRebecca Truty, Nila Patil, Raman Sankar, et al.
Clinical and Translational Gastroenterology|October 8, 2021
Clinical Impact of Pathogenic Germline Variants in Pancreatic Cancer: Results From a Multicenter, Prospective, Universal Genetic Testing StudyPedro L S Uson, N Jewel Samadder, Douglas Riegert-Johnson, et al.
JCO Global Oncology|July 22, 2022
Germline Pathogenic Variant Prevalence Among Latin American and US Hispanic Individuals Undergoing Testing for Hereditary Breast and Ovarian Cancer: A Cross-Sectional StudyCarlos Andrés Ossa Gomez, Maria Isabel Achatz, Mabel Hurtado, et al.
Nature Genetics|June 21, 2022
Single-cell analyses define a continuum of cell state and composition changes in the malignant transformation of polyps to colorectal cancerWinston R Becker, Stephanie A Nevins, Derek C Chen, et al.
JCO Precision Oncology|July 12, 2021
Multigene Panel Testing in Individuals With Hepatocellular Carcinoma Identifies Pathogenic Germline VariantsAnya Mezina, Neil Philips, Zoe Bogus, et al.
Human Genomics|July 9, 2025
Phenome-wide association study identifies multiple traits associated with a polygenic risk score for colorectal cancerElisabeth A Rosenthal, Wei-Qi Wei, Yuan Luo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardizationCeleste Eno, Pinar Bayrak-Toydemir, Lora Bean, et al.
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