Author

Andrew J. Cole

Harvard UniversityORCID 0000-0002-0828-826XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Assay:imaging· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aaron E. L. WarreniD· 1 shared Ahmad A. BeydouniD· 1 shared Alica M. GoldmaniD· 1 shared Alison AndersoniD· 1 shared Andrew R. PinesiD· 1 shared Annika B. FauconiD· 1 shared Antonio GambardellaiD· 1 shared Artemis IatrouiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperNeuroscience

Aaron E. L. WarrenORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintJul 22, 2026

A Brain Circuit for Status Epilepticus

Neal M. Nolan, Payam Tabaee Damavandi, Joseph I. Turner…·Frederic L. W. V. J. Schaper

This study identifies a unified brain circuit associated with status epilepticus using multimodal lesion mapping and gene expression analysis, showing high accuracy in distinguishing SE from other lesion etiologies.

DOI 10.64898/2026.07.17.738338

humanimaging

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Genetic & Genomic MedicineNature NeurosciencePeer-reviewedOct 1, 2024

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Epi25 Collaborative, Siwei Chen, Bassel W Abou-Khalil…·Alica M. Goldman

This study identifies shared and distinct ultra-rare genetic risk factors for epilepsy subtypes using whole-exome sequencing of 20,979 patients and 33,444 controls.

72 citationstop 1%

humanwhole-exome sequencing

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