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Connection

Jon Grant to Genetic Testing

This is a "connection" page, showing publications Jon Grant has written about Genetic Testing.
Connection Strength

0.301
  1. Validating data from multiplex assays of variant effect: A CanVIG-UK national survey of NHS clinical scientists. Am J Hum Genet. 2025 Jun 05; 112(6):1479-1488.
    View in: PubMed
    Score: 0.172
  2. Availability of benign missense variant "truthsets" for validation of functional assays: Current status and a systematic approach. Am J Hum Genet. 2025 Oct 02; 112(10):2281-2294.
    View in: PubMed
    Score: 0.044
  3. Quantifying evidence for phenotypic specificity (PP4) for syndromic phenotypes: Large-scale integration of rare germline FH variants from diagnostic laboratory testing for HLRCC and renal cancer. Genet Med. 2025 Nov; 27(11):101565.
    View in: PubMed
    Score: 0.044
  4. Classification of variants of reduced penetrance in high-penetrance cancer susceptibility genes: Framework for genetics clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group-UK). Genet Med. 2025 Feb; 27(2):101305.
    View in: PubMed
    Score: 0.041
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.