Author

Elizabeth E. Gerard

Northwestern UniversityORCID 0000-0003-3062-8360Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant effect prediction· 2 Approach:experimental assay· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alica M. GoldmaniD· 1 shared Amy R. Brooks‐KayaliD· 1 shared Andrea AccogliiD· 1 shared Andrea D. HildebrandiD· 1 shared Andrea L.C. SchneideriD· 1 shared Anna ChasseventiD· 1 shared Annalaura TorellaiD· 1 shared Colleen Gleason· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alica M. GoldmanORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintAug 21, 2026

Pathogenic Epilepsy Gene Variant Prevalence and Penetrance Among U.S. Military Veterans in the Million Veteran Program Cohort

Marissa A. Kellogg, Andrea D. Hildebrand, Tia DiNatale…·Craig Carl Teerlink

The paper examines the prevalence and penetrance of pathogenic variants in epilepsy genes among U.S. military Veterans, finding increased epilepsy risk for carriers of certain variants.

DOI 10.64898/2026.08.18.26360604

humanwhole-genome sequencing

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GeneticsBrainPeer-reviewedDec 16, 2021

Determining pathogenicity of variants of uncertain significance and identification of a founder variant in the epilepsy-associated gene, SZT2

Jeffrey Dennis Calhoun, Miriam C. Aziz, Hannah C. Happ…·Gemma L. Carvill

The paper identifies a founder variant in SZT2 associated with neurodevelopmental disorder and develops a method to distinguish pathogenic variants from VUSs in SZT2.

11 citations

humanwhole-exome sequencing

𝕏 PostBluesky