Search Results - "LINDEMAN, Neal"

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    Pathomic Fusion: An Integrated Framework for Fusing Histopathology and Genomic Features for Cancer Diagnosis and Prognosis by Chen, Richard J., Lu, Ming Y., Wang, Jingwen, Williamson, Drew F. K., Rodig, Scott J., Lindeman, Neal I., Mahmood, Faisal

    Published in IEEE transactions on medical imaging (01-04-2022)
    “…Cancer diagnosis, prognosis, mymargin and therapeutic response predictions are based on morphological information from histology slides and molecular profiles…”
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    Journal Article
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    Validation and Implementation of a Custom Next-Generation Sequencing Clinical Assay for Hematologic Malignancies by Kluk, Michael J, Lindsley, R. Coleman, Aster, Jon C, Lindeman, Neal I, Szeto, David, Hall, Dimity, Kuo, Frank C

    Published in The Journal of molecular diagnostics : JMD (01-07-2016)
    “…Targeted next-generation sequencing panels to identify genetic alterations in cancers are increasingly becoming an integral part of clinical practice. We…”
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    Worldwide Frequency of Commonly Detected EGFR Mutations by Graham, Rondell P, Treece, Amanda L, Lindeman, Neal I, Vasalos, Patricia, Shan, Mu, Jennings, Lawrence J, Rimm, David L

    “…- Recurrent epidermal growth factor receptor ( EGFR) mutations are seen in a subset of pulmonary adenocarcinomas. These mutations are targeted by EGFR…”
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    Natural history and molecular characteristics of lung cancers harboring EGFR exon 20 insertions by Oxnard, Geoffrey R, Lo, Peter C, Nishino, Mizuki, Dahlberg, Suzanne E, Lindeman, Neal I, Butaney, Mohit, Jackman, David M, Johnson, Bruce E, Jänne, Pasi A

    Published in Journal of thoracic oncology (01-02-2013)
    “…Exon 20 insertions are the third most common family of epidermal growth factor receptor (EGFR) mutations found in non-small-cell lung cancer (NSCLC). Little is…”
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    Clinical and Technical Aspects of Genomic Diagnostics for Precision Oncology by Sheikine, Yuri, Kuo, Frank C, Lindeman, Neal I

    Published in Journal of clinical oncology (20-03-2017)
    “…The emergence of precision medicine has been predicated on significant recent advances in diagnostic technology, particularly the advent of next-generation…”
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    BreaKmer: detection of structural variation in targeted massively parallel sequencing data using kmers by Abo, Ryan P, Ducar, Matthew, Garcia, Elizabeth P, Thorner, Aaron R, Rojas-Rudilla, Vanesa, Lin, Ling, Sholl, Lynette M, Hahn, William C, Meyerson, Matthew, Lindeman, Neal I, Van Hummelen, Paul, MacConaill, Laura E

    Published in Nucleic acids research (18-02-2015)
    “…Genomic structural variation (SV), a common hallmark of cancer, has important predictive and therapeutic implications. However, accurately detecting SV using…”
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