Selected Publications


Kv1.1 channel subunits in the control of neurocardiac function
Glasscock E.
Channels 2019, 13:299-307.

Cardiorespiratory profiling reveals primary breathing dysfunction in Kcna1-null mice: Implications for sudden unexpected death in epilepsy
Dhaibar H, Gautier NM, Chernyshev OY, Dominic P, Glasscock E.
Neurobiology of Disease 2019, 127:502-511.

Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice
Si M, Trosclair K, Hamilton KA, Glasscock E.
American Journal of Physiology- Cell Physiology 2019, 316:C154-C161.


Simultaneous video-EEG-ECG monitoring to identify neurocardiac dysfunction in mouse models of epilepsy.
*Mishra V, *Gautier NM, Glasscock E.
Journal of Visualized Experiments 2018, 131: e57300.

Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy.
Vanhoof-Villalba SL, Gautier NM, Mishra V, Glasscock E.
Epilepsia 2018, 59:358-368.


Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP).
Mishra V, Karumuri BK, Gautier NM, Liu R, Hutson TN, Vanhoof-Villalba SL, Vlachos I, Iasemidis L, Glasscock E.
Human Molecular Genetics 2017, 26:2091-2103.
*article highlighted in Epilepsy Currents 2017, 17:306-310.


Severe respiratory changes at end stage in a FUS-induced disease state in adult rats.
Jackson KL, Dhaibar HA, Dayton RD, Cananzi SG, Mayhan WG, Glasscock E, Klein RL.
BMC Neuroscience 2016, 17:69.

Gradient index microlens implanted in prefrontal cortex of mouse does not affect behavioral test performance over time
Lee S, Holly K, Voziyanov V, Villalba S, Grigsby H, Glasscock E, Vlachos I, Murray T.
PLoS One 2016, 11: e0146533.


Expression and function of Kv1.1 potassium channels in human atria from patients with atrial fibrillation.
Glasscock E, Voigt N, McCauley MD, Sun Q, Li N, Chiang DY, Zhou X-B, Molina CE, Thomas D, Schmidt C, Skapura DG, Noebels JL, Dobrev D, Wehrens XHT.
Basic Research in Cardiology 2015, 110: 505.

Spontaneous seizures in Kcna1-null mice lacking voltage-gated Kv1.1 channels activate Fos expression in select limbic circuits.
Gautier N, Glasscock E.
Journal of Neurochemistry 2015, 135: 157-164.


Genomic biomarkers of SUDEP in brain and heart.
Glasscock E.
Epilepsy & Behavior 2014, 38: 172-179.
*article highlighted by Neurology Advisor


Transcompartmental reversal of single fiber hyperexcitability in juxtaparanodal Kv1.1-deficient vagus nerve axons by activation of nodal KCNQ channels.
Glasscock E, Qian J, Kole MJ, Noebels JL.
The Journal of Physiology 2012, 590: 3913-26.

Kv1.1 potassium channel deficiency reveals brain-driven cardiac dysfunction as a candidate mechanism for sudden unexplained death in epilepsy.
Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL.
The Journal of Neuroscience 2010, 30: 5167-5175.
*article highlighted as Editors’ Choice in the journal Science Translational Medicine; feature “This Week in The Journal” article for the Neurobiology of Disease section of the Journal of Neuroscience.

Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.
Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL.
Science Translational Medicine 2009, 1: 2ra6.

When a disease gene is not really a disease gene.
Glasscock E, Noebels JL.
Future Neurology 2008, 3: 103-106.

Masking epilepsy by combining two epilepsy genes.
Glasscock E, Qian J, Yoo JW, Noebels JL.
Nature Neuroscience 2007, 10: 1554-1558.
*article highlighted by Faculty of 1000.

The mei-P26 gene encodes a RING finger B-box coiled-coil-NHL protein that regulates seizure susceptibility in Drosophilia.
Glasscock E, Singhania A, Tanouye MA.
Genetics 2005, 170: 1677-1689.

Drosophila couch potato mutants exhibit complex neurological abnormalities including epilepsy phenotypes.
Glasscock E, Tanouye MA.
Genetics 2005, 169: 2137-2149.

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