Last Updated: 09/26/2026
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Found 64 publications
Low-Allele-Frequency Somatic Variants in a Cohort of Sporadic Saccular "Berry" Cerebral Aneurysms.
Journal: Journal of the American Heart Association
Published: September 11, 2025
Longitudinal profiling identifies co-occurring BRCA1/2 reversions, TP53BP1, RIF1 and PAXIP1 mutations in PARP inhibitor-resistant advanced breast cancer.
Journal: Annals of oncology : official journal of the European Society for Medical Oncology
Published: January 20, 2024
NOTCH3 C201R variant causes cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) that can be confused with early-onset Alzheimer's disease.
Journal: Journal of the neurological sciences
Published: April 23, 2023
Homozygous CADPS2 Mutations Cause Neurodegenerative Disease with Lewy Body-like Pathology in Parrots.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 08, 2022
An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 22, 2022
Safety, Feasibility, and Merits of Longitudinal Molecular Testing of Multiple Metastatic Sites to Inform mTNBC Patient Treatment in the Intensive Trial of Omics in Cancer.
Journal: JCO precision oncology
Published: March 16, 2022
Somatic Mosaicism of a PDGFRB Activating Variant in Aneurysms of the Intracranial, Coronary, Aortic, and Radial Artery Vascular Beds.
Journal: Journal of the American Heart Association
Published: February 14, 2022
Corrigendum to "Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations" [Contemporary Clinical Trials 106 (2021) 106432].
Journal: Contemporary clinical trials
Published: February 06, 2022
Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 04, 2021
ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 05, 2021
Last Updated: 09/26/2026