BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: 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: 17] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Chenausky KV, Tager-Flusberg H. The importance of deep speech phenotyping for neurodevelopmental and genetic disorders: a conceptual review. J Neurodev Disord 2022;14:36. [PMID: 35690736 DOI: 10.1186/s11689-022-09443-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Yang X, Yin H, Wang X, Sun Y, Bian X, Zhang G, Li A, Cao A, Li B, Ebrahimi-fakhari D, Yang Z, Meisler MH, Liu Q. Social Deficits and Cerebellar Degeneration in Purkinje Cell Scn8a Knockout Mice. Front Mol Neurosci 2022;15:822129. [DOI: 10.3389/fnmol.2022.822129] [Reference Citation Analysis]
3 Tosti E, Boni R, Gallo A. Pathophysiological Responses to Conotoxin Modulation of Voltage-Gated Ion Currents. Marine Drugs 2022;20:282. [DOI: 10.3390/md20050282] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Picci G, Marchesan S, Caltagirone C. Ion Channels and Transporters as Therapeutic Agents: From Biomolecules to Supramolecular Medicinal Chemistry. Biomedicines 2022;10:885. [DOI: 10.3390/biomedicines10040885] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
5 Ma Z, Eaton M, Liu Y, Zhang J, Chen X, Tu X, Shi Y, Que Z, Wettschurack K, Zhang Z, Shi R, Chen Y, Kimbrough A, Lanman NA, Schust L, Huang Z, Yang Y. Deficiency of autism-related Scn2a gene in mice disrupts sleep patterns and circadian rhythms. Neurobiol Dis 2022;:105690. [PMID: 35301122 DOI: 10.1016/j.nbd.2022.105690] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Cutts A, Savoie H, Hammer MF, Schreiber J, Grayson C, Luzon C, Butterfield N, Pimstone SN, Aycardi E, Harden C, Yonan C, Jen E, Nguyen T, Carmack T, Haubenberger D. Clinical Characteristics and Treatment Experience of Individuals with SCN8A Developmental and Epileptic Encephalopathy (SCN8A-DEE): Findings from an Online Caregiver Survey. Seizure 2022. [DOI: 10.1016/j.seizure.2022.03.008] [Reference Citation Analysis]
7 Zheng X, Li H, Hu Z, Su D, Yang J. Structural and functional characterization of an achromatopsia-associated mutation in a phototransduction channel. Commun Biol 2022;5:190. [PMID: 35233102 DOI: 10.1038/s42003-022-03120-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Kalkman RK, Briaire JJ, Dekker DMT, Frijns JHM. The relation between polarity sensitivity and neural degeneration in a computational model of cochlear implant stimulation. Hear Res 2021;:108413. [PMID: 34952734 DOI: 10.1016/j.heares.2021.108413] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Wong JC, Butler KM, Shapiro L, Thelin JT, Mattison KA, Garber KB, Goldenberg PC, Kubendran S, Schaefer GB, Escayg A. Pathogenic in-Frame Variants in SCN8A: Expanding the Genetic Landscape of SCN8A-Associated Disease. Front Pharmacol 2021;12:748415. [PMID: 34867351 DOI: 10.3389/fphar.2021.748415] [Reference Citation Analysis]
10 Miralles RM, Patel MK. It Takes Two to Tango: Channel Interplay Leads to Paradoxical Hyperexcitability in a Loss-of-Function Epilepsy Variant. Epilepsy Curr. [DOI: 10.1177/15357597211057966] [Reference Citation Analysis]
11 Panagiotakos G, Pasca SP. A matter of space and time: Emerging roles of disease-associated proteins in neural development. Neuron 2021:S0896-6273(21)00865-5. [PMID: 34847355 DOI: 10.1016/j.neuron.2021.10.035] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
12 Xian J, Parthasarathy S, Ruggiero SM, Balagura G, Fitch E, Helbig K, Gan J, Ganesan S, Kaufman MC, Ellis CA, Lewis-Smith D, Galer P, Cunningham K, O'Brien M, Cosico M, Baker K, Darling A, Veiga de Goes F, El Achkar CM, Doering JH, Furia F, García-Cazorla Á, Gardella E, Geertjens L, Klein C, Kolesnik-Taylor A, Lammertse H, Lee J, Mackie A, Misra-Isrie M, Olson H, Sexton E, Sheidley B, Smith L, Sotero L, Stamberger H, Syrbe S, Thalwitzer KM, van Berkel A, van Haelst M, Yuskaitis C, Weckhuysen S, Prosser B, Son Rigby C, Demarest S, Pierce S, Zhang Y, Møller RS, Bruining H, Poduri A, Zara F, Verhage M, Striano P, Helbig I. Assessing the landscape of STXBP1-related disorders in 534 individuals. Brain 2021:awab327. [PMID: 35190816 DOI: 10.1093/brain/awab327] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
13 Nicole S, Lory P. New Challenges Resulting From the Loss of Function of Nav1.4 in Neuromuscular Diseases. Front Pharmacol 2021;12:751095. [PMID: 34671263 DOI: 10.3389/fphar.2021.751095] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
14 Talwar D, Hammer MF. SCN8A Epilepsy, Developmental Encephalopathy, and Related Disorders. Pediatr Neurol 2021;122:76-83. [PMID: 34353676 DOI: 10.1016/j.pediatrneurol.2021.06.011] [Reference Citation Analysis]
15 Ganguly S, Thompson CH, George AL Jr. Enhanced slow inactivation contributes to dysfunction of a recurrent SCN2A mutation associated with developmental and epileptic encephalopathy. J Physiol 2021. [PMID: 34287911 DOI: 10.1113/JP281834] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
16 Carpenter JC, Lignani G. Gene Editing and Modulation: the Holy Grail for the Genetic Epilepsies? Neurotherapeutics 2021. [PMID: 34235638 DOI: 10.1007/s13311-021-01081-y] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
17 Yu W, Smolen CE, Hill SF, Meisler MH. Spontaneous seizures and elevated seizure susceptibility in response to somatic mutation of sodium channel Scn8a in the mouse. Hum Mol Genet 2021;30:902-7. [PMID: 33822038 DOI: 10.1093/hmg/ddab092] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]