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The Journal of Molecular Diagnostics : JMD|December 27, 2016
A Targeted High-Throughput Next-Generation Sequencing Panel for Clinical Screening of Mutations, Gene Amplifications, and Fusions in Solid TumorsRajyalakshmi Luthra, Keyur P Patel, Mark J Routbort, et al.
Cancer Research|February 27, 2009
Sonic hedgehog signaling pathway is activated in ALK-positive anaplastic large cell lymphomaRajesh R Singh, Jeong Hee Cho-Vega, Yogesh Davuluri, et al.
Thyroid : Official Journal of the American Thyroid Association|October 28, 2016
Real-Time Genomic Characterization Utilizing Circulating Cell-Free DNA in Patients with Anaplastic Thyroid CarcinomaVlad C Sandulache, Michelle D Williams, Stephen Y Lai, et al.
Plos One|September 18, 2018
Clinical molecular testing for ASXL1 c.1934dupG p.Gly646fs mutation in hematologic neoplasms in the NGS eraSantiago Montes-Moreno, Mark J Routbort, Elijah J Lohman, et al.
American Journal of Clinical Pathology|October 22, 2015
Clinical validation of a multipurpose assay for detection and genotyping of CALR mutations in myeloproliferative neoplasmsMeenakshi Mehrotra, Rajyalakshmi Luthra, Rajesh R Singh, et al.
Plos One|August 3, 2017
Versatile ion S5XL sequencer for targeted next generation sequencing of solid tumors in a clinical laboratoryMeenakshi Mehrotra, Dzifa Yawa Duose, Rajesh R Singh, et al.
The Journal of Molecular Diagnostics : JMD|May 31, 2012
Detection of high-frequency and novel DNMT3A mutations in acute myeloid leukemia by high-resolution melting curve analysisRajesh R Singh, Ashish Bains, Keyur P Patel, et al.
The Journal of Molecular Diagnostics : JMD|July 2, 2013
Clinical validation of a next-generation sequencing screen for mutational hotspots in 46 cancer-related genesRajesh R Singh, Keyur P Patel, Mark J Routbort, et al.
American Journal of Hematology|January 22, 2014
BRAF kinase domain mutations are present in a subset of chronic myelomonocytic leukemia with wild-type RASLiping Zhang, Rajesh R Singh, Keyur P Patel, et al.
The Journal of Molecular Diagnostics : JMD|July 10, 2016
Comprehensive Screening of Gene Copy Number Aberrations in Formalin-Fixed, Paraffin-Embedded Solid Tumors Using Molecular Inversion Probe-Based Single-Nucleotide Polymorphism ArrayRajesh R Singh, Meenakshi Mehrotra, Hui Chen, et al.
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