Connection

JEFFREY NOEBELS to Epilepsy

This is a "connection" page, showing publications JEFFREY NOEBELS has written about Epilepsy.
Connection Strength

9.344
  1. The complex molecular epileptogenesis landscape of glioblastoma. Cell Rep Med. 2024 Aug 20; 5(8):101691.
    View in: PubMed
    Score: 0.546
  2. A hyperthermic seizure unleashes a surge of spreading depolarizations in Scn1a-deficient mice. JCI Insight. 2023 08 08; 8(15).
    View in: PubMed
    Score: 0.509
  3. Loss of functional System x-c uncouples aberrant postnatal neurogenesis from epileptogenesis in the hippocampus of Kcna1-KO mice. Cell Rep. 2022 11 22; 41(8):111696.
    View in: PubMed
    Score: 0.484
  4. Predicting the impact of sodium channel mutations in human brain disease. Epilepsia. 2019 12; 60 Suppl 3:S8-S16.
    View in: PubMed
    Score: 0.394
  5. Precision physiology and rescue of brain ion channel disorders. J Gen Physiol. 2017 May 01; 149(5):533-546.
    View in: PubMed
    Score: 0.329
  6. The Epilepsy Spectrum: Targeting Future Research Challenges. Cold Spring Harb Perspect Med. 2016 07 01; 6(7).
    View in: PubMed
    Score: 0.311
  7. Single-Gene Determinants of Epilepsy Comorbidity. Cold Spring Harb Perspect Med. 2015 Nov 02; 5(11).
    View in: PubMed
    Score: 0.297
  8. Early rescue of interneuron disease trajectory in developmental epilepsies. Curr Opin Neurobiol. 2016 Feb; 36:82-8.
    View in: PubMed
    Score: 0.297
  9. Pathway-driven discovery of epilepsy genes. Nat Neurosci. 2015 Mar; 18(3):344-50.
    View in: PubMed
    Score: 0.283
  10. Bexarotene reduces network excitability in models of Alzheimer's disease and epilepsy. Neurobiol Aging. 2014 Sep; 35(9):2091-5.
    View in: PubMed
    Score: 0.266
  11. Neonatal estradiol stimulation prevents epilepsy in Arx model of X-linked infantile spasms syndrome. Sci Transl Med. 2014 Jan 22; 6(220):220ra12.
    View in: PubMed
    Score: 0.262
  12. How can advances in epilepsy genetics lead to better treatments and cures? Adv Exp Med Biol. 2014; 813:309-17.
    View in: PubMed
    Score: 0.261
  13. Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology. 2013 Mar 19; 80(12):1078-85.
    View in: PubMed
    Score: 0.246
  14. Tau loss attenuates neuronal network hyperexcitability in mouse and Drosophila genetic models of epilepsy. J Neurosci. 2013 Jan 23; 33(4):1651-9.
    View in: PubMed
    Score: 0.245
  15. Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy. Cell. 2011 Jun 24; 145(7):1036-48.
    View in: PubMed
    Score: 0.219
  16. A perfect storm: Converging paths of epilepsy and Alzheimer's dementia intersect in the hippocampal formation. Epilepsia. 2011 Jan; 52 Suppl 1:39-46.
    View in: PubMed
    Score: 0.212
  17. "Jasper's Basic Mechanisms of the Epilepsies" Workshop. Epilepsia. 2010 Dec; 51 Suppl 5:1-5.
    View in: PubMed
    Score: 0.211
  18. Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death. Sci Transl Med. 2009 Oct 14; 1(2):2ra6.
    View in: PubMed
    Score: 0.195
  19. 2006 Merritt Putnam Symposium: mapping epileptic circuitry. Epilepsia. 2008; 49 Suppl 3:1-2.
    View in: PubMed
    Score: 0.172
  20. Masking epilepsy by combining two epilepsy genes. Nat Neurosci. 2007 Dec; 10(12):1554-8.
    View in: PubMed
    Score: 0.171
  21. The Judith Hoyer Lecture: genes, pixels, patterns, and prevention. Epilepsy Behav. 2006 Nov; 9(3):379-85.
    View in: PubMed
    Score: 0.158
  22. Invited comments on the Shostak and Ottman review. Epilepsia. 2006 Oct; 47(10):1750-1; author reply 1755-6.
    View in: PubMed
    Score: 0.158
  23. Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006 Feb; 21(2):93-8.
    View in: PubMed
    Score: 0.151
  24. WONOEP appraisal: Targeted therapy development for early onset epilepsies. Epilepsia. 2025 Feb; 66(2):328-340.
    View in: PubMed
    Score: 0.139
  25. WONOEP appraisal: Genetic insights into early onset epilepsies. Epilepsia. 2024 Nov; 65(11):3138-3154.
    View in: PubMed
    Score: 0.137
  26. Abnormal patterns of sleep and waking behaviors are accompanied by neocortical oscillation disturbances in an Ank3 mouse model of epilepsy-bipolar disorder comorbidity. Transl Psychiatry. 2023 Dec 20; 13(1):403.
    View in: PubMed
    Score: 0.130
  27. Targeted suppression of mTORC2 reduces seizures across models of epilepsy. Nat Commun. 2023 11 14; 14(1):7364.
    View in: PubMed
    Score: 0.130
  28. WWOX P47T partial loss-of-function mutation induces epilepsy, progressive neuroinflammation, and cerebellar degeneration in mice phenocopying human SCAR12. Prog Neurobiol. 2023 04; 223:102425.
    View in: PubMed
    Score: 0.123
  29. The biology of epilepsy genes. Annu Rev Neurosci. 2003; 26:599-625.
    View in: PubMed
    Score: 0.122
  30. Sodium channel gene expression and epilepsy. Novartis Found Symp. 2002; 241:109-20; discussion 120-3, 226-32.
    View in: PubMed
    Score: 0.114
  31. Modeling human epilepsies in mice. Epilepsia. 2001; 42 Suppl 5:11-5.
    View in: PubMed
    Score: 0.106
  32. Ion channels and epilepsy in man and mouse. Curr Opin Genet Dev. 2000 Jun; 10(3):286-91.
    View in: PubMed
    Score: 0.102
  33. 2017 WONOEP appraisal: Studying epilepsy as a network disease using systems biology approaches. Epilepsia. 2019 06; 60(6):1045-1053.
    View in: PubMed
    Score: 0.095
  34. Single-gene models of epilepsy. Adv Neurol. 1999; 79:227-38.
    View in: PubMed
    Score: 0.092
  35. 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. 2017 11; 58 Suppl 4:53-67.
    View in: PubMed
    Score: 0.085
  36. Ankyrin-G isoform imbalance and interneuronopathy link epilepsy and bipolar disorder. Mol Psychiatry. 2017 10; 22(10):1464-1472.
    View in: PubMed
    Score: 0.080
  37. Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. PLoS One. 2016; 11(9):e0162883.
    View in: PubMed
    Score: 0.079
  38. Targeting epilepsy genes. Neuron. 1996 Feb; 16(2):241-4.
    View in: PubMed
    Score: 0.076
  39. Molecular and cellular plasticity in developing epileptic brain. Cold Spring Harb Symp Quant Biol. 1996; 61:319-26.
    View in: PubMed
    Score: 0.075
  40. Sudden unexpected death in epilepsy: Identifying risk and preventing mortality. Epilepsia. 2015 Nov; 56(11):1700-6.
    View in: PubMed
    Score: 0.074
  41. Compromised maturation of GABAergic inhibition underlies abnormal network activity in the hippocampus of epileptic Ca2+ channel mutant mice, tottering. Pflugers Arch. 2015 Apr; 467(4):737-52.
    View in: PubMed
    Score: 0.068
  42. Ion channels in genetic and acquired forms of epilepsy. J Physiol. 2013 Feb 15; 591(4):753-64.
    View in: PubMed
    Score: 0.060
  43. WONOEP XI: Workshop summary by the Scientific Organizing Committee. Epilepsia. 2012 Jul; 53(7):1275-6.
    View in: PubMed
    Score: 0.058
  44. Identification of new epilepsy treatments: issues in preclinical methodology. Epilepsia. 2012 Mar; 53(3):571-82.
    View in: PubMed
    Score: 0.057
  45. Genetic and phenotypic heterogeneity of inherited spike-wave epilepsy: two mutant gene loci with independent cerebral excitability defects. Brain Res. 1991 Jul 26; 555(1):43-50.
    View in: PubMed
    Score: 0.055
  46. Synchronous hippocampal bursting reveals network excitability defects in an epilepsy gene mutation. Proc Natl Acad Sci U S A. 1991 Jun 01; 88(11):4736-40.
    View in: PubMed
    Score: 0.055
  47. Abbreviated report of the NIH/NINDS workshop on sudden unexpected death in epilepsy. Neurology. 2011 May 31; 76(22):1932-8.
    View in: PubMed
    Score: 0.054
  48. Mutational analysis of spike-wave epilepsy phenotypes. Epilepsy Res Suppl. 1991; 4:201-12.
    View in: PubMed
    Score: 0.053
  49. Deletion of the potassium channel Kv12.2 causes hippocampal hyperexcitability and epilepsy. Nat Neurosci. 2010 Sep; 13(9):1056-8.
    View in: PubMed
    Score: 0.052
  50. Genetic testing in the epilepsies--report of the ILAE Genetics Commission. Epilepsia. 2010 Apr; 51(4):655-70.
    View in: PubMed
    Score: 0.050
  51. Curing epilepsy: progress and future directions. Epilepsy Behav. 2009 Mar; 14(3):438-45.
    View in: PubMed
    Score: 0.047
  52. Aberrant excitatory neuronal activity and compensatory remodeling of inhibitory hippocampal circuits in mouse models of Alzheimer's disease. Neuron. 2007 Sep 06; 55(5):697-711.
    View in: PubMed
    Score: 0.042
  53. Genetics of epilepsy: epilepsy research foundation workshop report. Epileptic Disord. 2007 Jun; 9(2):194-236.
    View in: PubMed
    Score: 0.041
  54. Mutational analysis of inherited epilepsies. Adv Neurol. 1986; 44:97-113.
    View in: PubMed
    Score: 0.038
  55. Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy. Nat Neurosci. 2005 Aug; 8(8):1059-68.
    View in: PubMed
    Score: 0.036
  56. Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy. Elife. 2025 Jan 06; 13.
    View in: PubMed
    Score: 0.035
  57. Isolating single genes of the inherited epilepsies. Ann Neurol. 1984; 16 Suppl:S18-21.
    View in: PubMed
    Score: 0.033
  58. Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction. J Neurosci. 2003 Jan 15; 23(2):622-31.
    View in: PubMed
    Score: 0.031
  59. Models for epilepsy and epileptogenesis: report from the NIH workshop, Bethesda, Maryland. Epilepsia. 2002 Nov; 43(11):1410-20.
    View in: PubMed
    Score: 0.030
  60. ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies. Epilepsia. 2002 Oct; 43(10):1262-7.
    View in: PubMed
    Score: 0.030
  61. Males with epilepsy, complete subcortical band heterotopia, and somatic mosaicism for DCX. Neurology. 2002 May 28; 58(10):1559-62.
    View in: PubMed
    Score: 0.029
  62. Future directions for epilepsy research. Neurology. 2001 Nov 13; 57(9):1536-42.
    View in: PubMed
    Score: 0.028
  63. Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome. Epilepsia. 2001 Sep; 42(9):1103-11.
    View in: PubMed
    Score: 0.028
  64. Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy. Proc Natl Acad Sci U S A. 2000 Jan 18; 97(2):865-70.
    View in: PubMed
    Score: 0.025
  65. Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering. Science. 1979 Jun 22; 204(4399):1334-6.
    View in: PubMed
    Score: 0.024
  66. Nonobligate role of early or sustained expression of immediate-early gene proteins c-fos, c-jun, and Zif/268 in hippocampal mossy fiber sprouting. J Neurosci. 1998 Nov 15; 18(22):9245-55.
    View in: PubMed
    Score: 0.023
  67. Epilepsy in mice deficient in the 65-kDa isoform of glutamic acid decarboxylase. Proc Natl Acad Sci U S A. 1997 Dec 09; 94(25):14060-5.
    View in: PubMed
    Score: 0.021
  68. Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice. Cell. 1997 Oct 03; 91(1):139-48.
    View in: PubMed
    Score: 0.021
  69. Genetic epilepsy model derived from common inbred mouse strains. Genetics. 1994 Oct; 138(2):481-9.
    View in: PubMed
    Score: 0.017
  70. Case records of the Massachusetts General Hospital. Case 18-2013: a 32-year-old woman with recurrent episodes of altered consciousness. N Engl J Med. 2013 Jun 13; 368(24):2304-12.
    View in: PubMed
    Score: 0.016
  71. Neuronal Elav-like (Hu) proteins regulate RNA splicing and abundance to control glutamate levels and neuronal excitability. Neuron. 2012 Sep 20; 75(6):1067-80.
    View in: PubMed
    Score: 0.015
  72. To share or not to share: a randomized trial of consent for data sharing in genome research. Genet Med. 2011 Nov; 13(11):948-55.
    View in: PubMed
    Score: 0.014
  73. Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture. J Neurosci. 2004 Apr 21; 24(16):4030-42.
    View in: PubMed
    Score: 0.008
  74. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet. 2000 Oct; 26(2):191-4.
    View in: PubMed
    Score: 0.007
  75. Upregulation of L-type Ca2+ channels in reactive astrocytes after brain injury, hypomyelination, and ischemia. J Neurosci. 1998 Apr 01; 18(7):2321-34.
    View in: PubMed
    Score: 0.005
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.