| Year |
Citation |
Score |
| 2021 |
Massey CA, Thompson SJ, Ostrom RW, Drabek J, Sveinsson OA, Tomson T, Haas EA, Mena OJ, Goldman AM, Noebels JL. X-linked serotonin 2C receptor is associated with a non-canonical pathway for sudden unexpected death in epilepsy. Brain Communications. 3: fcab149. PMID 34396109 DOI: 10.1093/braincomms/fcab149 |
0.34 |
|
| 2021 |
Aiba I, Noebels JL. Kcnq2/Kv7.2 controls the threshold and bihemispheric symmetry of cortical spreading depolarization. Brain : a Journal of Neurology. PMID 33768249 DOI: 10.1093/brain/awab141 |
0.356 |
|
| 2021 |
Loring KE, Mattiske T, Lee K, Zysk A, Jackson MR, Noebels JL, Shoubridge C. Early 17β-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX). Neurobiology of Disease. 105329. PMID 33711494 DOI: 10.1016/j.nbd.2021.105329 |
0.323 |
|
| 2020 |
Hatcher A, Yu K, Meyer J, Aiba I, Deneen B, Noebels JL. Pathogenesis of peritumoral hyperexcitability in an immunocompetent CRISPR-based glioblastoma model. The Journal of Clinical Investigation. PMID 32250339 DOI: 10.1172/Jci133316 |
0.311 |
|
| 2019 |
Miao QL, Herlitze S, Mark MD, Noebels JL. Adult loss of Cacna1a in mice recapitulates childhood absence epilepsy by distinct thalamic bursting mechanisms. Brain : a Journal of Neurology. PMID 31800012 DOI: 10.1093/brain/awz365 |
0.332 |
|
| 2019 |
Mahoney JM, Mills JD, Muhlebner A, Noebels J, Potschka H, Simonato M, Kobow K. 2017 WONOEP appraisal: Studying epilepsy as a network disease using systems biology approaches. Epilepsia. PMID 31087652 DOI: 10.1111/Epi.15216 |
0.376 |
|
| 2018 |
Ogiwara I, Miyamoto H, Tatsukawa T, Yamagata T, Nakayama T, Atapour N, Miura E, Mazaki E, Ernst SJ, Cao D, Ohtani H, Itohara S, Yanagawa Y, Montal M, Yuzaki M, ... ... Noebels JL, et al. Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice. Communications Biology. 1. PMID 30175250 DOI: 10.1038/s42003-018-0099-2 |
0.345 |
|
| 2018 |
Chen C, Holth JK, Bunton-Stasyshyn R, Anumonwo CK, Meisler MH, Noebels JL, Isom LL. deletion fails to rescue premature lethality in two models of sodium channel epilepsy. Annals of Clinical and Translational Neurology. 5: 982-987. PMID 30128323 DOI: 10.1002/Acn3.599 |
0.326 |
|
| 2018 |
Meyer J, Maheshwari A, Noebels J, Smirnakis S. Asynchronous suppression of visual cortex during absence seizures in stargazer mice. Nature Communications. 9: 1938. PMID 29769525 DOI: 10.1038/S41467-018-04349-8 |
0.412 |
|
| 2017 |
Moyer JT, Gnatkovsky V, Ono T, Otáhal J, Wagenaar J, Stacey WC, Noebels J, Ikeda A, Staley K, de Curtis M, Litt B, Galanopoulou AS. Standards for data acquisition and software-based analysis of in vivo electroencephalography recordings from animals. A TASK1-WG5 report of the AES/ILAE Translational Task Force of the ILAE. Epilepsia. 58: 53-67. PMID 29105070 DOI: 10.1111/Epi.13909 |
0.372 |
|
| 2017 |
Maheshwari A, Akbar A, Wang M, Marks R, Yu K, Park S, Foster BL, Noebels JL. Persistent aberrant cortical phase-amplitude coupling following seizure treatment in absence epilepsy models. The Journal of Physiology. PMID 28901011 DOI: 10.1113/Jp274696 |
0.327 |
|
| 2017 |
Lam AD, Deck G, Goldman A, Eskandar EN, Noebels J, Cole AJ. Silent hippocampal seizures and spikes identified by foramen ovale electrodes in Alzheimer's disease. Nature Medicine. PMID 28459436 DOI: 10.1038/Nm.4330 |
0.373 |
|
| 2017 |
Noebels J. Precision physiology and rescue of brain ion channel disorders. The Journal of General Physiology. 149: 533-546. PMID 28428202 DOI: 10.1085/Jgp.201711759 |
0.337 |
|
| 2016 |
Holmes GL, Noebels JL. The Epilepsy Spectrum: Targeting Future Research Challenges. Cold Spring Harbor Perspectives in Medicine. 6. PMID 27371672 DOI: 10.1101/Cshperspect.A028043 |
0.308 |
|
| 2016 |
Horváth A, Szűcs A, Barcs G, Noebels JL, Kamondi A. Epileptic Seizures in Alzheimer Disease: A Review. Alzheimer Disease and Associated Disorders. PMID 26756385 DOI: 10.1097/WAD.0000000000000134 |
0.302 |
|
| 2015 |
Noebels JL. Single-Gene Determinants of Epilepsy Comorbidity. Cold Spring Harbor Perspectives in Medicine. 5. PMID 26525453 DOI: 10.1101/cshperspect.a022756 |
0.324 |
|
| 2015 |
Lhatoo S, Noebels J, Whittemore V. Sudden unexpected death in epilepsy: Identifying risk and preventing mortality. Epilepsia. 56: 1700-6. PMID 26494436 DOI: 10.1111/Epi.13134 |
0.323 |
|
| 2015 |
Aiba I, Noebels JL. Spreading depolarization in the brainstem mediates sudden cardiorespiratory arrest in mouse SUDEP models. Science Translational Medicine. 7: 282ra46. PMID 25855492 DOI: 10.1126/Scitranslmed.Aaa4050 |
0.351 |
|
| 2015 |
Noebels J. Pathway-driven discovery of epilepsy genes. Nature Neuroscience. 18: 344-50. PMID 25710836 DOI: 10.1038/Nn.3933 |
0.426 |
|
| 2014 |
Maheshwari A, Noebels JL. Monogenic models of absence epilepsy: windows into the complex balance between inhibition and excitation in thalamocortical microcircuits. Progress in Brain Research. 213: 223-52. PMID 25194492 DOI: 10.1016/B978-0-444-63326-2.00012-0 |
0.373 |
|
| 2014 |
Qi Y, Wang J, Bomben VC, Li DP, Chen SR, Sun H, Xi Y, Reed JG, Cheng J, Pan HL, Noebels JL, Yeh ET. Hyper-SUMOylation of the Kv7 potassium channel diminishes the M-current leading to seizures and sudden death. Neuron. 83: 1159-71. PMID 25189211 DOI: 10.1016/j.neuron.2014.07.042 |
0.363 |
|
| 2014 |
Guerrini R, Noebels J. How can advances in epilepsy genetics lead to better treatments and cures? Advances in Experimental Medicine and Biology. 813: 309-17. PMID 25012387 DOI: 10.1007/978-94-017-8914-1_25 |
0.372 |
|
| 2014 |
Bomben V, Holth J, Reed J, Cramer P, Landreth G, Noebels J. Bexarotene reduces network excitability in models of Alzheimer's disease and epilepsy. Neurobiology of Aging. 35: 2091-5. PMID 24767949 DOI: 10.1016/J.Neurobiolaging.2014.03.029 |
0.346 |
|
| 2013 |
Chen TT, Klassen TL, Goldman AM, Marini C, Guerrini R, Noebels JL. Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology. 80: 1078-85. PMID 23408874 DOI: 10.1212/Wnl.0B013E31828868E7 |
0.348 |
|
| 2013 |
Holth JK, Bomben VC, Reed JG, Inoue T, Younkin L, Younkin SG, Pautler RG, Botas J, Noebels JL. Tau loss attenuates neuronal network hyperexcitability in mouse and Drosophila genetic models of epilepsy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 1651-9. PMID 23345237 DOI: 10.1523/Jneurosci.3191-12.2013 |
0.329 |
|
| 2013 |
Lerche H, Shah M, Beck H, Noebels J, Johnston D, Vincent A. Ion channels in genetic and acquired forms of epilepsy. The Journal of Physiology. 591: 753-64. PMID 23090947 DOI: 10.1113/Jphysiol.2012.240606 |
0.409 |
|
| 2012 |
Olivetti PR, Noebels JL. Interneuron, interrupted: molecular pathogenesis of ARX mutations and X-linked infantile spasms. Current Opinion in Neurobiology. 22: 859-65. PMID 22565167 DOI: 10.1016/j.conb.2012.04.006 |
0.31 |
|
| 2012 |
Holth J, Reed JG, Inoue T, Pautler R, Botas J, Noebels J. P1-283: Tau loss reduces hyperexcitability in mouse and drosophila genetics models of epilepsy Alzheimer's & Dementia. 8: P204-P204. DOI: 10.1016/J.Jalz.2012.05.563 |
0.357 |
|
| 2011 |
Klassen T, Davis C, Goldman A, Burgess D, Chen T, Wheeler D, McPherson J, Bourquin T, Lewis L, Villasana D, Morgan M, Muzny D, Gibbs R, Noebels J. Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy. Cell. 145: 1036-48. PMID 21703448 DOI: 10.1016/J.Cell.2011.05.025 |
0.362 |
|
| 2011 |
Noebels J. A perfect storm: Converging paths of epilepsy and Alzheimer's dementia intersect in the hippocampal formation. Epilepsia. 52: 39-46. PMID 21214538 DOI: 10.1111/j.1528-1167.2010.02909.x |
0.334 |
|
| 2010 |
Noebels JL, Avoli M, Rogawski M, Olsen R, Delgado-Escueta AV. "Jasper's Basic Mechanisms of the Epilepsies" Workshop. Epilepsia. 51: 1-5. PMID 21208201 DOI: 10.1111/J.1528-1167.2010.02792.X |
0.323 |
|
| 2010 |
Jiang YH, Pan Y, Zhu L, Landa L, Yoo J, Spencer C, Lorenzo I, Brilliant M, Noebels J, Beaudet AL. Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3. Plos One. 5: e12278. PMID 20808828 DOI: 10.1371/Journal.Pone.0012278 |
0.334 |
|
| 2010 |
Zhang X, Bertaso F, Yoo JW, Baumgärtel K, Clancy SM, Lee V, Cienfuegos C, Wilmot C, Avis J, Hunyh T, Daguia C, Schmedt C, Noebels J, Jegla T. Deletion of the potassium channel Kv12.2 causes hippocampal hyperexcitability and epilepsy. Nature Neuroscience. 13: 1056-8. PMID 20676103 DOI: 10.1038/Nn.2610 |
0.397 |
|
| 2010 |
Noebels JL. Isolating Epilepsy Genes and Their Comorbidiites Epilepsy & Seizure. 3: 72-83. DOI: 10.3805/EANDS.3.72 |
0.357 |
|
| 2009 |
Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL. Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death. Science Translational Medicine. 1: 2ra6. PMID 20368164 DOI: 10.1126/Scitranslmed.3000289 |
0.339 |
|
| 2009 |
Price MG, Yoo JW, Burgess DL, Deng F, Hrachovy RA, Frost JD, Noebels JL. A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 8752-63. PMID 19587282 DOI: 10.1523/JNEUROSCI.0915-09.2009 |
0.339 |
|
| 2009 |
Jacobs MP, Leblanc GG, Brooks-Kayal A, Jensen FE, Lowenstein DH, Noebels JL, Spencer DD, Swann JW. Curing epilepsy: progress and future directions. Epilepsy & Behavior : E&B. 14: 438-45. PMID 19341977 DOI: 10.1016/J.Yebeh.2009.02.036 |
0.323 |
|
| 2009 |
Ernst WL, Zhang Y, Yoo JW, Ernst SJ, Noebels JL. Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 1615-25. PMID 19211869 DOI: 10.1523/JNEUROSCI.2081-08.2009 |
0.32 |
|
| 2008 |
Singh NA, Otto JF, Dahle EJ, Pappas C, Leslie JD, Vilaythong A, Noebels JL, White HS, Wilcox KS, Leppert MF. Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization. The Journal of Physiology. 586: 3405-23. PMID 18483067 DOI: 10.1113/Jphysiol.2008.154971 |
0.374 |
|
| 2007 |
Glasscock E, Qian J, Yoo JW, Noebels JL. Masking epilepsy by combining two epilepsy genes. Nature Neuroscience. 10: 1554-8. PMID 17982453 DOI: 10.1038/Nn1999 |
0.365 |
|
| 2007 |
Sisodiya S, Cross JH, Blümcke I, Chadwick D, Craig J, Crino PB, Debenham P, Delanty N, Elmslie F, Gardiner M, Golden J, Goldstein D, Greenberg DA, Guerrini R, Hanna M, ... ... Noebels JL, et al. Genetics of epilepsy: epilepsy research foundation workshop report. Epileptic Disorders : International Epilepsy Journal With Videotape. 9: 194-236. PMID 17525034 DOI: 10.1684/Epd.2007.0107 |
0.315 |
|
| 2006 |
Noebels JL. The Judith Hoyer Lecture: genes, pixels, patterns, and prevention. Epilepsy & Behavior : E&B. 9: 379-85. PMID 17029973 DOI: 10.1016/j.yebeh.2006.08.018 |
0.321 |
|
| 2005 |
Noebels JL. Calcium channel "gaiting" and absence epilepsy. Epilepsy Currents / American Epilepsy Society. 5: 95-7. PMID 16145613 DOI: 10.1111/j.1535-7511.2005.05306.x |
0.352 |
|
| 2005 |
Cobos I, Calcagnotto ME, Vilaythong AJ, Thwin MT, Noebels JL, Baraban SC, Rubenstein JL. Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy. Nature Neuroscience. 8: 1059-68. PMID 16007083 DOI: 10.1038/nn1499 |
0.312 |
|
| 2003 |
Noebels JL. Exploring new gene discoveries in idiopathic generalized epilepsy. Epilepsia. 44: 16-21. PMID 12752457 DOI: 10.1046/J.1528-1157.44.S.2.4.X |
0.363 |
|
| 2002 |
Anderson E, Berkovic S, Dulac O, Gardiner M, Jain S, Laue Friis M, Lindhout D, Noebels J, Ottman R, Scaramelli A, Serratosa J, Steinlein O, Avanzini G, Bailey-Wilson J, Cardon L, et al. ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies. Epilepsia. 43: 1262-7. PMID 12366744 DOI: 10.1046/J.1528-1157.2002.29502.X |
0.341 |
|
| 2002 |
Noebels JL. Sodium channel gene expression and epilepsy. Novartis Foundation Symposium. 241: 109-20; discussion 1. PMID 11771641 DOI: 10.1002/0470846682.Ch8 |
0.316 |
|
| 2001 |
Noebels JL. Modeling human epilepsies in mice. Epilepsia. 42: 11-5. PMID 11887961 DOI: 10.1046/j.1528-1157.2001.0420s5011.x |
0.336 |
|
| 2001 |
Jacobs MP, Fischbach GD, Davis MR, Dichter MA, Dingledine R, Lowenstein DH, Morrell MJ, Noebels JL, Rogawski MA, Spencer SS, Theodore WH. Future directions for epilepsy research. Neurology. 57: 1536-42. PMID 11706087 DOI: 10.1212/Wnl.57.9.1536 |
0.34 |
|
| 2001 |
Heilstedt HA, Burgess DL, Anderson AE, Chedrawi A, Tharp B, Lee O, Kashork CD, Starkey DE, Wu YQ, Noebels JL, Shaffer LG, Shapira SK. Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome. Epilepsia. 42: 1103-11. PMID 11580756 DOI: 10.1046/J.1528-1157.2001.08801.X |
0.357 |
|
| 2001 |
Zwingman TA, Neumann PE, Noebels JL, Herrup K. Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 1169-78. PMID 11160387 DOI: 10.1523/Jneurosci.21-04-01169.2001 |
0.307 |
|
| 2000 |
Steinlein OK, Noebels JL. Ion channels and epilepsy in man and mouse. Current Opinion in Genetics & Development. 10: 286-91. PMID 10826987 DOI: 10.1016/S0959-437X(00)00079-4 |
0.334 |
|
| 1999 |
Noebels JL. Single-gene models of epilepsy. Advances in Neurology. 79: 227-38. PMID 10514817 |
0.342 |
|
| 1997 |
Kash SF, Johnson RS, Tecott LH, Noebels JL, Mayfield RD, Hanahan D, Baekkeskov S. Epilepsy in mice deficient in the 65-kDa isoform of glutamic acid decarboxylase. Proceedings of the National Academy of Sciences of the United States of America. 94: 14060-5. PMID 9391152 DOI: 10.1073/Pnas.94.25.14060 |
0.365 |
|
| 1997 |
Cox GA, Lutz CM, Yang CL, Biemesderfer D, Bronson RT, Fu A, Aronson PS, Noebels JL, Frankel WN. Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice. Cell. 91: 139-48. PMID 9335342 DOI: 10.1016/S0092-8674(01)80016-7 |
0.31 |
|
| 1996 |
Noebels JL, Sutherland ML, Nahm WK, DiPasquale E. Molecular and cellular plasticity in developing epileptic brain. Cold Spring Harbor Symposia On Quantitative Biology. 61: 319-26. PMID 9246461 DOI: 10.1101/Sqb.1996.061.01.035 |
0.309 |
|
| 1996 |
Noebels JL. Targeting epilepsy genes. Neuron. 16: 241-4. PMID 8789939 DOI: 10.1016/S0896-6273(00)80042-2 |
0.359 |
|
| 1995 |
Noebels JL. Single locus mutations in mice expressing generalized spike-wave absence epilepsies. Italian Journal of Neurological Sciences. 16: 107-11. PMID 7642343 DOI: 10.1007/BF02229082 |
0.329 |
|
| 1991 |
Qiao XX, Noebels JL. Genetic and phenotypic heterogeneity of inherited spike-wave epilepsy: two mutant gene loci with independent cerebral excitability defects. Brain Research. 555: 43-50. PMID 1933329 DOI: 10.1016/0006-8993(91)90857-R |
0.334 |
|
| 1990 |
Noebels JL, Qiao X, Bronson RT, Spencer C, Davisson MT. Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures. Epilepsy Research. 7: 129-35. PMID 2289471 DOI: 10.1016/0920-1211(90)90098-G |
0.331 |
|
| 1986 |
Noebels JL. Mutational analysis of inherited epilepsies. Advances in Neurology. 44: 97-113. PMID 2871726 |
0.362 |
|
| 1979 |
Noebels JL, Sidman RL. Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering. Science (New York, N.Y.). 204: 1334-6. PMID 572084 DOI: 10.1126/Science.572084 |
0.402 |
|
| 1979 |
Noebels JL. Analysis of inherited epilepsy using single locus mutations in mice. Federation Proceedings. 38: 2405-10. PMID 383515 |
0.375 |
|
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