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Connection

Kelly Stratton to Mutation

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

0.144
  1. Outcome of genetic evaluation of patients with kidney cancer referred for suspected hereditary cancer syndromes. Urol Oncol. 2016 May; 34(5):238.e1-7.
    View in: PubMed
    Score: 0.097
  2. Utility of prospective pathologic evaluation to inform clinical genetic testing for hereditary leiomyomatosis and renal cell carcinoma. Cancer. 2017 Jul 01; 123(13):2452-2458.
    View in: PubMed
    Score: 0.026
  3. A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome. PLoS Genet. 2013 Aug; 9(8):e1003695.
    View in: PubMed
    Score: 0.021
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.

THIS IS A DEVELOPMENT VERSION OF PROFILES. PLEASE GO TO THE PRODUCTION ENVIRONMENT FOR UPDATES