A citation-based method for searching scientific literature

S L Smart, V Lopantsev, C L Zhang, C A Robbins, H Wang, S Y Chiu, P A Schwartzkroin, A Messing, B L Tempel. Neuron 1998
Times Cited: 439



S M Zuberi, L H Eunson, A Spauschus, R De Silva, J Tolmie, N W Wood, R C McWilliam, J B Stephenson, D M Kullmann, M G Hanna. Brain 1999
Times Cited: 257




List of shared articles



Times cited

Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy.
Elisabetta Amadori, Giuditta Pellino, Lalit Bansal, Serena Mazzone, Rikke S Møller, Guido Rubboli, Pasquale Striano, Angelo Russo. Eur J Med Genet 2022
3

Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia.
Giorgia Dinoi, Michael Morin, Elena Conte, Hagar Mor Shaked, Maria Antonietta Coppola, Maria Cristina D'Adamo, Orly Elpeleg, Antonella Liantonio, Inbar Hartmann, Annamaria De Luca,[...]. Int J Mol Sci 2022
0

Sudden unexpected death in epilepsy: Respiratory mechanisms.
Frida A Teran, Eduardo Bravo, George B Richerson. Handb Clin Neurol 2022
0

Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel.
Paola Imbrici, Andrea Accogli, Rikard Blunck, Concetta Altamura, Michele Iacomino, Maria Cristina D'adamo, Anna Allegri, Marina Pedemonte, Noemi Brolatti, Stella Vari,[...]. Biomedicines 2021
2

Comparison of K+ Channel Families.
Jaume Taura, Daniel M Kircher, Isabel Gameiro-Ros, Paul A Slesinger. Handb Exp Pharmacol 2021
4

Kv1.1 channels mediate network excitability and feed-forward inhibition in local amygdala circuits.
Samrat Thouta, Yiming Zhang, Esperanza Garcia, Terrance P Snutch. Sci Rep 2021
4

Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia.
Edgard Verdura, Carme Fons, Agatha Schlüter, Montserrat Ruiz, Stéphane Fourcade, Carlos Casasnovas, Antonio Castellano, Aurora Pujol. J Med Genet 2020
17

Neuron-specific Kv1.1 deficiency is sufficient to cause epilepsy, premature death, and cardiorespiratory dysregulation.
Krystle Trosclair, Hemangini A Dhaibar, Nicole M Gautier, Vikas Mishra, Edward Glasscock. Neurobiol Dis 2020
17

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.
Kelsey Paulhus, Lauren Ammerman, Edward Glasscock. Int J Mol Sci 2020
34

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches.
Maria Cristina D'Adamo, Antonella Liantonio, Jean-Francois Rolland, Mauro Pessia, Paola Imbrici. Int J Mol Sci 2020
28

Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice.
Man Si, Krystle Trosclair, Kathryn A Hamilton, Edward Glasscock. Am J Physiol Cell Physiol 2019
8

Cardiorespiratory profiling reveals primary breathing dysfunction in Kcna1-null mice: Implications for sudden unexpected death in epilepsy.
Hemangini Dhaibar, Nicole M Gautier, Oleg Y Chernyshev, Paari Dominic, Edward Glasscock. Neurobiol Dis 2019
25


BAD knockout provides metabolic seizure resistance in a genetic model of epilepsy with sudden unexplained death in epilepsy.
Jeannine Foley, Veronica Burnham, Meghan Tedoldi, Nika N Danial, Gary Yellen. Epilepsia 2018
10

Accumulation of rest deficiency precedes sudden death of epileptic Kv1.1 knockout mice, a model of sudden unexpected death in epilepsy.
Shruthi H Iyer, Stephanie A Matthews, Timothy A Simeone, Rama Maganti, Kristina A Simeone. Epilepsia 2018
15

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou, Christopher A Reid. Pharmacol Rev 2018
119

Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy.
Stephanie L Vanhoof-Villalba, Nicole M Gautier, Vikas Mishra, Edward Glasscock. Epilepsia 2018
11

A novel metabolism-based phenotypic drug discovery platform in zebrafish uncovers HDACs 1 and 3 as a potential combined anti-seizure drug target.
Kingsley Ibhazehiebo, Cezar Gavrilovici, Cristiane L de la Hoz, Shun-Chieh Ma, Renata Rehak, Gaurav Kaushik, Paola L Meza Santoscoy, Lucas Scott, Nandan Nath, Do-Young Kim,[...]. Brain 2018
34


Kv1.1 channelopathy abolishes presynaptic spike width modulation by subthreshold somatic depolarization.
Umesh Vivekananda, Pavel Novak, Oscar D Bello, Yuri E Korchev, Shyam S Krishnakumar, Kirill E Volynski, Dimitri M Kullmann. Proc Natl Acad Sci U S A 2017
15

Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy.
Rocio Leal-Campanario, Luis Alarcon-Martinez, Hector Rieiro, Susana Martinez-Conde, Tugba Alarcon-Martinez, Xiuli Zhao, Jonathan LaMee, Pamela J Osborn Popp, Michael E Calhoun, Juan I Arribas,[...]. Sci Rep 2017
28

Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP).
Vikas Mishra, Bharat K Karumuri, Nicole M Gautier, Rui Liu, Timothy N Hutson, Stephanie L Vanhoof-Villalba, Ioannis Vlachos, Leonidas Iasemidis, Edward Glasscock. Hum Mol Genet 2017
31

Pharmacogenetic and case-control study on potassium channel related gene variants and genetic generalized epilepsy.
Jian Qu, Shao-Hua Lu, Zhi-Li Lu, Ping Xu, Da-Xiong Xiang, Qiang Qu. Medicine (Baltimore) 2017
5