Author

Ivy E. Dick

University of Maryland, BaltimoreORCID 0000-0002-7253-6846Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biophysics· 1 Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Research Focus:drug response / drug discovery· 1 Assay:electrophysiology· 1 Research Focus:host-pathogen & immune response· 1 Organism:mouse· 1

Frequent Co-Authors

Alexandra Valsamakis· 1 shared Alexandros PoulopoulosiD· 1 shared Ana-Octavia BusuiociD· 1 shared Andrea J. RomanowskiiD· 1 shared Andy GoldeniD· 1 shared Brian N. MathuriD· 1 shared Colin D. RobertsoniD· 1 shared Daiana C.O. VieiraiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandra Valsamakis

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Voltage Gated Calcium Channel Dysregulation May Contribute to Neurological Symptoms in Calmodulinopathies

John W. Hussey, Emily M. DeMarco, Deborah A. DiSilvestre, Malene Brohus, Ana-Octavia Busuioc, Emil Drivsholm Iversen, Helene Halkjær Jensen, Mette Nyegaard, Michael Toft Overgaard, Manu Ben-Johny, Ivy E. Dick

This study investigates how calmodulin mutations affect voltage-gated calcium channel regulation in neurons, linking these effects to neurological symptoms in calmodulinopathies.

The Journal of General Physiology · Mar 6, 2026Peer-reviewedBiophysics

A Natural History Study of Timothy Syndrome

Katherine W. Timothy, Rosemary Bauer, Kerry A. Larkin, Edward Patrick Walsh, Dominic James Abrams, M. Cecilia Gonzalez Corcia, Alexandra Valsamakis, Geoffrey S. Pitt, Ivy E. Dick, Andy Golden

This study describes the first natural history of Timothy syndrome, identifying common extra-cardiac features beyond cardiac issues.

Orphanet Journal of Rare Diseases · Nov 23, 2024Peer-reviewedGenetic & Genomic Medicine

Rapid modeling of an ultra-rare epilepsy patient variant in mice by in utero prime editing

Colin D. Robertson, Patrick W. Davis, Ryan R. Richardson, Philip H. Iffland, Daiana C.O. Vieira, Marilyn R. Steyert, Paige N. McKeon, Andrea J. Romanowski, Garrett W. Crutcher, Eldin Jašarević, Steffen B. E. Wolff, Brian N. Mathur, Peter B. Crino, Tracy L. Bale, Ivy E. Dick, Alexandros Poulopoulos

This paper describes a method to rapidly create mouse models of human epilepsy variants using in utero prime editing, enabling the study of seizures in a clinically relevant timeframe.

bioRxiv · Dec 6, 2023 · PreprintNeuroscience