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JTO Clinical and Research Reports|January 29, 2021
Ultrarapid EGFR Mutation Screening Followed by Comprehensive Next-Generation Sequencing: A Feasible, Informative Approach for Lung Carcinoma Cytology Specimens With a High Success RateMaria E Arcila, Soo-Ryum Yang, Amir Momeni, et al.
Research Square|August 7, 2024
Maximizing the clinical utility and performance of cytology samples for comprehensive genetic profiling - A report on the impact of process optimization through the analysis of 4,871 cytology samples profiled by MSK-IMPACTDavid Kim, Chad Vanderbilt, Soo-Ryum Yang, et al.
The American Journal of Surgical Pathology|January 26, 2013
Dedifferentiation in gastrointestinal stromal tumor to an anaplastic KIT-negative phenotype: a diagnostic pitfall: morphologic and molecular characterization of 8 cases occurring either de novo or after imatinib therapyCristina R Antonescu, Salvatore Romeo, Lei Zhang, et al.
The Journal of Molecular Diagnostics : JMD|July 15, 2014
Detection of mutations in myeloid malignancies through paired-sample analysis of microdroplet-PCR deep sequencing dataDonavan T Cheng, Janice Cheng, Talia N Mitchell, et al.
Genes, Chromosomes & Cancer|June 3, 2015
Consistent copy number changes and recurrent PRKAR1A mutations distinguish Melanotic Schwannomas from Melanomas: SNP-array and next generation sequencing analysisLu Wang, Ahmet Zehir, Justyna Sadowska, et al.
Head and Neck Pathology|June 17, 2024
DNA Mutational and Copy Number Variation Profiling of Primary Craniofacial Osteosarcomas by Next-Generation SequencingGord Guo Zhu, Chuanyong Lu, Ivana Petrovic, et al.
The Journal of Molecular Diagnostics : JMD|December 21, 2020
Rapid EGFR Mutation Detection Using the Idylla Platform: Single-Institution Experience of 1200 Cases Analyzed by an In-House Developed Pipeline and Comparison with Concurrent Next-Generation Sequencing ResultsAmir Momeni-Boroujeni, Paulo Salazar, Tao Zheng, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 23, 2011
EGFR exon 19 insertions: a new family of sensitizing EGFR mutations in lung adenocarcinomaMai He, Marzia Capelletti, Khedoudja Nafa, et al.
Journal of the National Cancer Institute|October 16, 2003
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemiaKenneth Offit, Orna Levran, Brian Mullaney, et al.
JCO Precision Oncology|September 14, 2018
Reliable Pan-Cancer Microsatellite Instability Assessment by Using Targeted Next-Generation Sequencing DataSumit Middha, Liying Zhang, Khedoudja Nafa, et al.
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