Area of research
Genetics · Cancer Research
Research interest
Research interests include Cancer Genomics and Diagnostics, Glioma Diagnosis and Treatment, Genomics and Rare Diseases, and Prenatal Screening and Diagnostics.
Genomic data in the All of Us Research Program
3-hour genome sequencing and targeted analysis to rapidly assess genetic risk
SARS-CoV-2 Diversity and Transmission on a University Campus across Two Academic Years during the Pandemic
Diagnosis of Ovarian Carcinoma Homologous Recombination DNA Repair Deficiency From Targeted Gene Capture Oncology Assays
Genomic surveillance of SARS-CoV-2 Omicron variants on a university campus
Comparison of Symptoms and RNA Levels in Children and Adults With SARS-CoV-2 Infection in the Community Setting
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care
Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma
Call for improvement in medical school training in genetics: results of a national survey
SwabExpress: An End-to-End Protocol for Extraction-Free COVID-19 Testing
Predictors of mortality and tumor recurrence in desmoplastic infantile ganglioglioma and astrocytoma—and individual participant data meta-analysis (IPDMA)
Comparable Specimen Collection from Both Ends of At-Home Midturbinate Swabs
Histone deposition pathways determine the chromatin landscapes of H3.1 and H3.3 K27M oncohistones
Preliminary support for a "dry swab, extraction free" protocol for SARS-CoV-2 testing via RT-qPCR.
eScholarship (California Digital Library) 2020cited by 46position: middle
Pan-Trk Immunohistochemistry Identifies NTRK Rearrangements in Pediatric Mesenchymal Tumors
Expanding the Spectrum of Pediatric NTRK-rearranged Mesenchymal Tumors
Microsatellite instability in prostate cancer by PCR or next-generation sequencing
Desmoplastic Infantile Ganglioglioma/Astrocytoma (DIG/DIA) Are Distinct Entities with Frequent BRAFV600 Mutations
The Undergraduate Training in Genomics (UTRIG) Initiative: Early & Active Training for Physicians in the Genomic Medicine Era
Infantile <i>NTRK</i> -associated Mesenchymal Tumors
T-cell clonality assessment by next-generation sequencing improves detection sensitivity in mycosis fungoides
Detection of Gene Rearrangements in Targeted Clinical Next-Generation Sequencing
Detection of FLT3 Internal Tandem Duplication in Targeted, Short-Read-Length, Next-Generation Sequencing Data