LabCompass
Mid career · publishing since 2004

Publications

143

Citations

5,338

Est. group size

~8

Recurring co-author estimate

Active years

23

Publishing since 2004

Research summary
AI-generated

Kristy Lee's research focuses on clinical and genomic medicine, particularly how genetic variants are classified, interpreted, and used in patient care. Work spans topics such as classifying disease-causing gene variants (including for cancer syndromes and bleeding disorders), evaluating secondary findings from genomic sequencing, and studying patient and clinician perspectives on genetic testing and gene therapy. Much of this work involves large collaborative consortia developing standards for interpreting genetic test results.

Clinical variant classification and curationGenomic secondary findings and actionabilityHereditary cancer and hemostasis geneticsGenetic counseling and patient perspectivesGenomic sequencing in clinical diagnosis

Publication output rose notably from 2017 to a peak around 2021-2022, then declined somewhat before increasing again in 2025, suggesting an overall active but variable publication pattern over the past decade.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026

Publication cadence
Publications per year over the last 10 years — averaging 9.8/year recently
2017: 3 publications172018: 14 publications182019: 5 publications192020: 14 publications202021: 26 publications26212022: 22 publications222023: 6 publications232024: 8 publications242025: 12 publications252026: 1 publication26
Recent publications
Publishes in
  • Genetics in Medicine×20
  • Molecular Genetics and Metabolism×9
  • UNC Libraries×9
  • Cancer Genetics×8
  • Human Mutation×5
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This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.

Last updated Jul 19, 2026.

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