LabCompass

Kayla Treat

Biochemistry, Genetics and Molecular Biology · Indiana University

OpenAlex
Genomics and Rare DiseasesGenomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental DisordersRNA modifications and cancerGenetic Syndromes and Imprinting

Publications

37

Citations

397

Est. group size

~8

Recurring co-author estimate

Active years

33

Publishing since 1994

Research summary
AI-generated

Kayla Treat studies rare genetic and developmental disorders, focusing on identifying and interpreting DNA variants that cause conditions affecting the nervous system and development. This work spans laboratory investigation of gene function and clinical genetics, including how families understand genetic test results. The research bridges molecular biology and patient-oriented (clinical) genetics.

Rare genetic diseasesNeurodevelopmental disordersGenetic variant interpretationClinical and community geneticsGene function in syndromes

Publication activity has grown noticeably over the last several years, rising from about one paper per year early on to roughly five to eight per year more recently.

Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026

Publication cadence
Publications per year over the last 10 years — averaging 5.4/year recently
172018: 1 publication182019: 1 publication192020: 2 publications202021: 1 publication212022: 4 publications222023: 5 publications232024: 8 publications8242025: 8 publications8252026: 2 publications26
Recent publications
Publishes in
  • Genetics in Medicine Open×9
  • American Journal of Medical Genetics Part A×3
  • Clinical Genetics×2
  • Molecular Case Studies×2
  • medRxiv×2

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 11, 2026.

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