BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Mishra V, Karumuri BK, Gautier NM, Liu R, Hutson TN, Vanhoof-Villalba SL, Vlachos I, Iasemidis L, Glasscock E. Scn2a deletion improves survival and brain-heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP). Hum Mol Genet 2017;26:2091-103. [PMID: 28334922 DOI: 10.1093/hmg/ddx104] [Cited by in Crossref: 32] [Cited by in F6Publishing: 28] [Article Influence: 6.4] [Reference Citation Analysis]
Number Citing Articles
1 Liu R, Vlachos I. Mutual information in the frequency domain for the study of biological systems. Biomedical Signal Processing and Control 2018;46:268-80. [DOI: 10.1016/j.bspc.2018.08.006] [Cited by in Crossref: 2] [Article Influence: 0.5] [Reference Citation Analysis]
2 Meisler MH, Hill SF, Yu W. Sodium channelopathies in neurodevelopmental disorders. Nat Rev Neurosci 2021;22:152-66. [PMID: 33531663 DOI: 10.1038/s41583-020-00418-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
3 Focken T, Burford K, Grimwood ME, Zenova A, Andrez JC, Gong W, Wilson M, Taron M, Decker S, Lofstrand V, Chowdhury S, Shuart N, Lin S, Goodchild SJ, Young C, Soriano M, Tari PK, Waldbrook M, Nelkenbrecher K, Kwan R, Lindgren A, de Boer G, Lee S, Sojo L, DeVita RJ, Cohen CJ, Wesolowski SS, Johnson JP Jr, Dehnhardt CM, Empfield JR. Identification of CNS-Penetrant Aryl Sulfonamides as Isoform-Selective NaV1.6 Inhibitors with Efficacy in Mouse Models of Epilepsy. J Med Chem 2019;62:9618-41. [PMID: 31525968 DOI: 10.1021/acs.jmedchem.9b01032] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
4 Hutson TN, Rezaei F, Gautier NM, Indumathy J, Glasscock E, Iasemidis L. Directed Connectivity Analysis of the Neuro-Cardio- and Respiratory Systems Reveals Novel Biomarkers of Susceptibility to SUDEP. IEEE Open J Eng Med Biol 2020;1:301-11. [PMID: 34223181 DOI: 10.1109/ojemb.2020.3036544] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Symonds JD, Zuberi SM. WITHDRAWN: Genetics update: Monogenetics, polygene disorders and the quest for modifying genes. Neuropharmacology 2017:S0028-3908(17)30347-7. [PMID: 28757052 DOI: 10.1016/j.neuropharm.2017.07.016] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
6 Mantegazza M, Cestèle S, Catterall WA. Sodium channelopathies of skeletal muscle and brain. Physiol Rev 2021;101:1633-89. [PMID: 33769100 DOI: 10.1152/physrev.00025.2020] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
7 Vanhoof-Villalba SL, Gautier NM, Mishra V, Glasscock E. Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy. Epilepsia 2018;59:358-68. [PMID: 29265344 DOI: 10.1111/epi.13978] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]
8 Iyer SH, Aggarwal A, Warren TJ, Hallgren J, Abel PW, Simeone TA, Simeone KA. Progressive cardiorespiratory dysfunction in Kv1.1 knockout mice may provide temporal biomarkers of pending sudden unexpected death in epilepsy (SUDEP): The contribution of orexin. Epilepsia 2020;61:572-88. [PMID: 32030748 DOI: 10.1111/epi.16434] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
9 Dhaibar H, Gautier NM, Chernyshev OY, Dominic P, Glasscock E. Cardiorespiratory profiling reveals primary breathing dysfunction in Kcna1-null mice: Implications for sudden unexpected death in epilepsy. Neurobiol Dis 2019;127:502-11. [PMID: 30974168 DOI: 10.1016/j.nbd.2019.04.006] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 7.0] [Reference Citation Analysis]
10 Mishra V, Gautier NM, Glasscock E. Simultaneous Video-EEG-ECG Monitoring to Identify Neurocardiac Dysfunction in Mouse Models of Epilepsy. J Vis Exp 2018. [PMID: 29443088 DOI: 10.3791/57300] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
11 [DOI: 10.1101/2021.02.02.429423] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
12 Zhang Z, Qiu W, Gong H, Li G, Jiang Q, Liang P, Zheng H, Zhang P. Low-intensity ultrasound suppresses low-Mg 2+ -induced epileptiform discharges in juvenile mouse hippocampal slices. J Neural Eng 2019;16:036006. [DOI: 10.1088/1741-2552/ab0b9a] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
13 Indumathy J, Pruitt A, Gautier NM, Crane K, Glasscock E. Kv1.1 deficiency alters repetitive and social behaviors in mice and rescues autistic-like behaviors due to Scn2a haploinsufficiency. Brain Behav 2021;11:e02041. [PMID: 33484493 DOI: 10.1002/brb3.2041] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
14 Trosclair K, Si M, Watts M, Gautier NM, Voigt N, Traylor J, Bitay M, Baczko I, Dobrev D, Hamilton KA, Bhuiyan MS, Dominic P, Glasscock E. Kv1.1 potassium channel subunit deficiency alters ventricular arrhythmia susceptibility, contractility, and repolarization. Physiol Rep 2021;9:e14702. [PMID: 33427415 DOI: 10.14814/phy2.14702] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Oyrer J, Maljevic S, Scheffer IE, Berkovic SF, Petrou S, Reid CA. Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies. Pharmacol Rev 2018;70:142-73. [PMID: 29263209 DOI: 10.1124/pr.117.014456] [Cited by in Crossref: 92] [Cited by in F6Publishing: 73] [Article Influence: 23.0] [Reference Citation Analysis]
16 Gano LB, Grabenstatter HL. Modulation of Abnormal Sodium Channel Currents in Heart and Brain: Hope for SUDEP Prevention and Seizure Reduction. Epilepsy Curr 2017;17:306-10. [PMID: 29225548 DOI: 10.5698/1535-7597.17.5.306] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
17 O’leary T. Homeostasis, failure of homeostasis and degenerate ion channel regulation. Current Opinion in Physiology 2018;2:129-38. [DOI: 10.1016/j.cophys.2018.01.006] [Cited by in Crossref: 20] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
18 Si M, Trosclair K, Hamilton KA, Glasscock E. Genetic ablation or pharmacological inhibition of Kv1.1 potassium channel subunits impairs atrial repolarization in mice. Am J Physiol Cell Physiol 2019;316:C154-61. [PMID: 30427720 DOI: 10.1152/ajpcell.00335.2018] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
19 Sahly AN, Shevell M, Sadleir LG, Myers KA. SUDEP risk and autonomic dysfunction in genetic epilepsies. Auton Neurosci 2021;237:102907. [PMID: 34773737 DOI: 10.1016/j.autneu.2021.102907] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
20 Li R, Buchanan GF. Scurrying to Understand Sudden Expected Death in Epilepsy: Insights From Animal Models. Epilepsy Curr 2019;19:390-6. [PMID: 31526023 DOI: 10.1177/1535759719874787] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
21 Ren Y, Chang J, Li C, Jia C, Li P, Wang Y, Chu XP. The Effects of Ketogenic Diet Treatment in Kcna1-Null Mouse, a Model of Sudden Unexpected Death in Epilepsy. Front Neurol 2019;10:744. [PMID: 31354612 DOI: 10.3389/fneur.2019.00744] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
22 Trosclair K, Dhaibar HA, Gautier NM, Mishra V, Glasscock E. Neuron-specific Kv1.1 deficiency is sufficient to cause epilepsy, premature death, and cardiorespiratory dysregulation. Neurobiol Dis 2020;137:104759. [PMID: 31978607 DOI: 10.1016/j.nbd.2020.104759] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 6.0] [Reference Citation Analysis]
23 Symonds JD, Zuberi SM. Genetics update: Monogenetics, polygene disorders and the quest for modifying genes. Neuropharmacology 2018;132:3-19. [PMID: 29037745 DOI: 10.1016/j.neuropharm.2017.10.013] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]
24 Yu Y, Yang Z, Jin B, Qin X, Zhu X, Sun J, Huo L, Wang R, Shi Y, Jia Z, Shi YS, Chu S, Kong D, Zhang W. Cannabidiol inhibits febrile seizure by modulating AMPA receptor kinetics through its interaction with the N-terminal domain of GluA1/GluA2. Pharmacological Research 2020;161:105128. [DOI: 10.1016/j.phrs.2020.105128] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
25 Glasscock E. Kv1.1 channel subunits in the control of neurocardiac function. Channels (Austin) 2019;13:299-307. [PMID: 31250689 DOI: 10.1080/19336950.2019.1635864] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
26 Spratt PWE, Alexander RPD, Ben-Shalom R, Sahagun A, Kyoung H, Keeshen CM, Sanders SJ, Bender KJ. Paradoxical hyperexcitability from NaV1.2 sodium channel loss in neocortical pyramidal cells. Cell Rep 2021;36:109483. [PMID: 34348157 DOI: 10.1016/j.celrep.2021.109483] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
27 Paulhus K, Ammerman L, Glasscock E. Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity. Int J Mol Sci 2020;21:E2802. [PMID: 32316562 DOI: 10.3390/ijms21082802] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 7.0] [Reference Citation Analysis]
28 Jones JE, Asato MR, Brown MG, Doss JL, Felton EA, Kearney JA, Talos D, Dacks PA, Whittemore V, Poduri A; NINDS/AES Benchmarks Stewards Committee. Epilepsy Benchmarks Area IV: Limit or Prevent Adverse Consequence of Seizures and Their Treatment Across the Life Span. Epilepsy Curr 2020;20:31S-9S. [PMID: 31973592 DOI: 10.1177/1535759719895277] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Spratt PWE, Ben-Shalom R, Keeshen CM, Burke KJ Jr, Clarkson RL, Sanders SJ, Bender KJ. The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex. Neuron 2019;103:673-685.e5. [PMID: 31230762 DOI: 10.1016/j.neuron.2019.05.037] [Cited by in Crossref: 59] [Cited by in F6Publishing: 51] [Article Influence: 19.7] [Reference Citation Analysis]
30 Léna I, Mantegazza M. NaV1.2 haploinsufficiency in Scn2a knock-out mice causes an autistic-like phenotype attenuated with age. Sci Rep 2019;9:12886. [PMID: 31501495 DOI: 10.1038/s41598-019-49392-7] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
31 D'Adamo MC, Liantonio A, Conte E, Pessia M, Imbrici P. Ion Channels Involvement in Neurodevelopmental Disorders. Neuroscience 2020;440:337-59. [PMID: 32473276 DOI: 10.1016/j.neuroscience.2020.05.032] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 4.5] [Reference Citation Analysis]