Last Updated: 09/26/2026
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Found 11 publications
Massively Scalable Single-cell Multiomic Profiling of T Cell Repertoire with REFLEX.
Journal: Research square
Published: January 09, 2026
REFLEX, a Novel Immune Profiling Assay, Combining TCR Repertoire and Multiome at Massively Scalable Single-cell Resolution to Catapult Exploration of T-cell Derived Immunity.
Journal: bioRxiv : the preprint server for biology
Published: December 15, 2025
Restoring RUNX1 deficiency in RUNX1 familial platelet disorder by inhibiting its degradation.
Journal: Blood advances
Published: June 18, 2020
Consideration for Employer-Based and Geographic Attributes Included in Value Assessment Methods of Next-Generation Sequencing Tests.
Journal: Journal of managed care & specialty pharmacy
Published: July 27, 2019
Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests.
Journal: Journal of genetic counseling
Published: July 19, 2019
Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 01, 2019
Projected Cost-Effectiveness for 2 Gene-Drug Pairs Using a Multigene Panel for Patients Undergoing Percutaneous Coronary Intervention.
Journal: Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
Published: January 27, 2019
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 24, 2019
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 19, 2018
Activating PAX gene family paralogs to complement PAX5 leukemia driver mutations.
Journal: PLoS genetics
Published: March 05, 2018
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Last Updated: 09/26/2026