Jeffrey D Calhoun

6PUBLICATIONS
18CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Genomics and transcriptomicsNeurogenetics
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Publications (6)

|Jul 21, 2026
Analysis of 14q12 microdeletions reveals novel regulatory loci for the neurodevelopmental disorder-related gene FOXG1.

|Jul 09, 2026
An integrated, scaled approach to resolve TSC2 variants of uncertain significance.

|Feb 06, 2026
An integrated, scaled approach to resolve TSC2 variants of uncertain significance.

Carina G Biar, Ziyu R Wang, Nathan D Camp

|Jun 19, 2024
Multimodal framework to resolve variants of uncertain significance in TSC2.

Carina G Biar, Cole Pfeifer, Gemma L Carvill

|Apr 01, 2020
CACNA1H variants are not a cause of monogenic epilepsy.

Jeffrey D Calhoun, Alexandra M Huffman, Irena Bellinski

|Sep 25, 2018
Unravelling the genetic architecture of autosomal recessive epilepsy in the genomic era.

Jeffrey D Calhoun, Gemma L Carvill

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Frequent Collaborators

4 joint publications

Gemma L Carvill

3 joint publications

Carina G Biar

1 joint publications

Jennifer A Kearney

1 joint publications

Nathan D Camp