Author

Rahil A. Tai

The University of Texas Health Science Center at Houston

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Assay:electronic health records· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Alison Merket· 1 shared Anu CherukaraiD· 1 shared Christian M. BoßelmanniD· 1 shared Costin LeuiD· 1 shared Dennis LaliD· 1 shared Elizabete SilvaiD· 1 shared Emily A. HuthiD· 1 shared Gary Taylor· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alison Merket

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Author profile →

1 paper

Recent·Most cited

Underutilization of Syndrome-Specific ICD-10 Codes for Genetic Epilepsies: Implications for Precision Medicine

Elizabete Silva, Tobias Brünger, Gary Taylor, Mousumi Sinha, Alison Merket, Anu Cherukara, Sunanjay Bajaj, Jessica Clark, Ludovica Montanucci, Emily A. Huth, Mariana Fauteux, Samden D. Lhatoo, Christian M. Boßelmann, Costin Leu, Rahil A. Tai, Dennis Lal

This study evaluates the underutilization of syndrome-specific ICD-10 codes for monogenic epilepsies in clinical practice, finding that less than two-thirds of patients with molecular diagnoses were assigned these codes.

Epilepsia · Mar 26, 2026Peer-reviewedGenetic & Genomic Medicine