Author

Leann Smith DaWalt

University of Wisconsin–MadisonORCID 0000-0002-0376-4095Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Assay:electronic health records· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Aditi GuptaiD· 1 shared Allyson Schreiber· 1 shared Anna M. AbbacchiiD· 1 shared Christina A. GurnettiD· 1 shared Daleep Grewal· 1 shared Dustin BaldridgeiD· 1 shared Heather C. HazlettiD· 1 shared John Nicholas ConstantinoiD· 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

Aditi GuptaORCID

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1 paper

Recent·Most cited

Neurobehavioral Profiles and Clinical Consequences of MYT1L-Related Neurodevelopmental Disorder: Insights from the Brain Gene Registry.

Jorge Luis Granadillo, Levi Kaster, Virginia Lanzotti, Daleep Grewal, Allyson Schreiber, Anna M. Abbacchi, Christina A. Gurnett, Kristen L. Kroll, Dustin Baldridge, Heather C. Hazlett, Leann Smith DaWalt, John Nicholas Constantino, Aditi Gupta, Joseph D. Dougherty

This study characterizes MYT1L-Related Neurodevelopmental Disorder using data from the Brain Gene Registry, identifying cognitive, behavioral, and clinical features in affected individuals.

American Journal of Medical Genetics Part A · Oct 19, 2026Peer-reviewedGenetic & Genomic Medicine