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Connection

Kristen Deak to Mutation

This is a "connection" page, showing publications Kristen Deak has written about Mutation.
Connection Strength

0.361
  1. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4. Neurology. 2007 Feb 20; 68(8):578-82.
    View in: PubMed
    Score: 0.134
  2. Acute myeloid leukemia arising from polycythemia vera underwent reversion to chronic phase of myeloproliferative neoplasm status post chemotherapy: Biclonal myeloid neoplasms with genomic evidence of a common early hematopoietic progenitor. Hematol Oncol. 2021 Apr; 39(2):254-257.
    View in: PubMed
    Score: 0.087
  3. CSGALNACT1-congenital disorder of glycosylation: A mild skeletal dysplasia with advanced bone age. Hum Mutat. 2020 03; 41(3):655-667.
    View in: PubMed
    Score: 0.082
  4. Automated next-generation profiling of genomic alterations in human cancers. Nat Commun. 2022 05 20; 13(1):2830.
    View in: PubMed
    Score: 0.024
  5. Pulmonary Granular Cell Tumors: A Study of 4 Cases Including a Malignant Phenotype. Am J Surg Pathol. 2019 10; 43(10):1397-1402.
    View in: PubMed
    Score: 0.020
  6. False positives in multiplex PCR-based next-generation sequencing have unique signatures. J Mol Diagn. 2014 Sep; 16(5):541-549.
    View in: PubMed
    Score: 0.014
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.