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Connection

Peter Pytel to High-Throughput Nucleotide Sequencing

This is a "connection" page, showing publications Peter Pytel has written about High-Throughput Nucleotide Sequencing.
  1. Identification of Molecular Alterations Challenging Initial Pathologic Classification in Cases of Clinician-Initiated Next-Generation Sequencing Testing. Am J Clin Pathol. 2021 Nov 08; 156(6):1007-1018.
    View in: PubMed
    Score: 0.640
  2. Integrating a Large Next-Generation Sequencing Panel into the Clinical Diagnosis of Gliomas Provides a Comprehensive Platform for Classification from FFPE Tissue or Smear Preparations. J Neuropathol Exp Neurol. 2019 03 01; 78(3):257-267.
    View in: PubMed
    Score: 0.531
  3. Clear Cell Papillary Cystadenoma of the Ovary Masquerading as Metastatic Clear Cell Renal Cell Carcinoma: A Case Report and Review of the Literature. Int J Gynecol Pathol. 2021 May 01; 40(3):290-295.
    View in: PubMed
    Score: 0.039
  4. High prevalence of MiTF staining in undifferentiated pleomorphic sarcoma: caution in the use of melanocytic markers in sarcoma. Histopathology. 2017 Apr; 70(5):734-745.
    View in: PubMed
    Score: 0.029
  5. Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy. Circ Cardiovasc Genet. 2014 Dec; 7(6):751-759.
    View in: PubMed
    Score: 0.024
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.