J Mol Diagn
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Publication Venue For
- RNA Sequencing Identifies Novel NRG1 Fusions in Solid Tumors that Lack Co-Occurring Oncogenic Drivers. 2023
- Next-Generation Sequencing Concordance Analysis of Comprehensive Solid Tumor Profiling between a Centralized Specialty Laboratory and the Decentralized Personal Genome Diagnostics elio Tissue Complete Kitted Solution.. 23:1324-1333. 2021
- Nanopore Flongle Sequencing as a Rapid, Single-Specimen Clinical Test for Fusion Detection.. 23:630-636. 2021
- Identifying End Users' Preferences about Structuring Pharmacogenetic Test Orders in an Electronic Health Record System.. 22:1264-1271. 2020
- Analytical Evaluation of the Abbott RealTime CT/NG Assay for Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Rectal and Pharyngeal Swabs.. 22:811-816. 2020
- Preanalytical Variables for the Genomic Assessment of the Cellular and Acellular Fractions of the Liquid Biopsy in a Cohort of Breast Cancer Patients.. 22:319-337. 2020
- A Model Information Management Plan for Molecular Pathology Sequence Data Using Standards: From Sequencer to Electronic Health Record.. 21:408-417. 2019
- A Nanopore Sequencing-Based Assay for Rapid Detection of Gene Fusions.. 21:58-69. 2019
- Development and Verification of an RNA Sequencing (RNA-Seq) Assay for the Detection of Gene Fusions in Tumors.. 20:495-511. 2018
- Deciphering Elevated Microsatellite Alterations at Selected Tetra/Pentanucleotide Repeats, Microsatellite Instability, and Loss of Heterozygosity in Colorectal Cancers.. 20:366-372. 2018
- Authors' Reply.. 20:125-126. 2018
- Differences in Microsatellite Instability Profiles between Endometrioid and Colorectal Cancers: A Potential Cause for False-Negative Results?. 19:57-64. 2017
- Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists.. 19:4-23. 2017
- A Proof-of-Concept Case Study for Personalized Noninvasive Prenatal Diagnosis: Can We Put It to Work?. 17:483-486. 2015
- False positives in multiplex PCR-based next-generation sequencing have unique signatures.. 16:541-549. 2014
- Development and clinical validation of a real-time PCR assay for PITX2 DNA methylation to predict prostate-specific antigen recurrence in prostate cancer patients following radical prostatectomy.. 15:270-279. 2013
- Genes with bimodal expression are robust diagnostic targets that define distinct subtypes of epithelial ovarian cancer with different overall survival.. 14:214-222. 2012
- Donor cell leukemia in umbilical cord blood transplant patients: a case study and literature review highlighting the importance of molecular engraftment analysis.. 12:530-537. 2010
- Ultrasensitive detection of KRAS2 mutations in bile and serum from patients with biliary tract carcinoma using LigAmp technology.. 11:583-589. 2009