Connection

JEFFREY NOEBELS to Humans

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

0.591
  1. The complex molecular epileptogenesis landscape of glioblastoma. Cell Rep Med. 2024 Aug 20; 5(8):101691.
    View in: PubMed
    Score: 0.026
  2. Glioblastoma disrupts cortical network activity at multiple spatial and temporal scales. Nat Commun. 2024 May 27; 15(1):4503.
    View in: PubMed
    Score: 0.025
  3. Arx expansion mutation perturbs cortical development by augmenting apoptosis without activating innate immunity in a mouse model of X-linked infantile spasms syndrome. Dis Model Mech. 2020 03 30; 13(3).
    View in: PubMed
    Score: 0.019
  4. Predicting the impact of sodium channel mutations in human brain disease. Epilepsia. 2019 12; 60 Suppl 3:S8-S16.
    View in: PubMed
    Score: 0.019
  5. Precision physiology and rescue of brain ion channel disorders. J Gen Physiol. 2017 May 01; 149(5):533-546.
    View in: PubMed
    Score: 0.016
  6. The Epilepsy Spectrum: Targeting Future Research Challenges. Cold Spring Harb Perspect Med. 2016 07 01; 6(7).
    View in: PubMed
    Score: 0.015
  7. Hippocampal abnormalities and sudden childhood death. Forensic Sci Med Pathol. 2016 06; 12(2):198-9.
    View in: PubMed
    Score: 0.014
  8. Single-Gene Determinants of Epilepsy Comorbidity. Cold Spring Harb Perspect Med. 2015 Nov 02; 5(11).
    View in: PubMed
    Score: 0.014
  9. Early rescue of interneuron disease trajectory in developmental epilepsies. Curr Opin Neurobiol. 2016 Feb; 36:82-8.
    View in: PubMed
    Score: 0.014
  10. Pathway-driven discovery of epilepsy genes. Nat Neurosci. 2015 Mar; 18(3):344-50.
    View in: PubMed
    Score: 0.013
  11. How can advances in epilepsy genetics lead to better treatments and cures? Adv Exp Med Biol. 2014; 813:309-17.
    View in: PubMed
    Score: 0.012
  12. Monogenic models of absence epilepsy: windows into the complex balance between inhibition and excitation in thalamocortical microcircuits. Prog Brain Res. 2014; 213:223-52.
    View in: PubMed
    Score: 0.012
  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: 0.012
  14. Interneuron, interrupted: molecular pathogenesis of ARX mutations and X-linked infantile spasms. Curr Opin Neurobiol. 2012 Oct; 22(5):859-65.
    View in: PubMed
    Score: 0.011
  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: 0.010
  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: 0.010
  17. "Jasper's Basic Mechanisms of the Epilepsies" Workshop. Epilepsia. 2010 Dec; 51 Suppl 5:1-5.
    View in: PubMed
    Score: 0.010
  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: 0.009
  19. Expanded alternative splice isoform profiling of the mouse Cav3.1/alpha1G T-type calcium channel. BMC Mol Biol. 2009 May 29; 10:53.
    View in: PubMed
    Score: 0.009
  20. T-type calcium channels: from discovery to channelopathies, 25 years of research. Channels (Austin). 2008 Jul-Aug; 2(4):299-302.
    View in: PubMed
    Score: 0.008
  21. 2006 Merritt Putnam Symposium: mapping epileptic circuitry. Epilepsia. 2008; 49 Suppl 3:1-2.
    View in: PubMed
    Score: 0.008
  22. The Judith Hoyer Lecture: genes, pixels, patterns, and prevention. Epilepsy Behav. 2006 Nov; 9(3):379-85.
    View in: PubMed
    Score: 0.007
  23. Invited comments on the Shostak and Ottman review. Epilepsia. 2006 Oct; 47(10):1750-1; author reply 1755-6.
    View in: PubMed
    Score: 0.007
  24. 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: 0.007
  25. Genetic mouse models of essential tremor: are they essential? J Clin Invest. 2005 Mar; 115(3):584-6.
    View in: PubMed
    Score: 0.007
  26. Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy. Elife. 2025 Jan 06; 13.
    View in: PubMed
    Score: 0.007
  27. WONOEP appraisal: Targeted therapy development for early onset epilepsies. Epilepsia. 2025 Feb; 66(2):328-340.
    View in: PubMed
    Score: 0.007
  28. WONOEP appraisal: Genetic insights into early onset epilepsies. Epilepsia. 2024 Nov; 65(11):3138-3154.
    View in: PubMed
    Score: 0.006
  29. Histone serotonylation regulates ependymoma tumorigenesis. Nature. 2024 Aug; 632(8026):903-910.
    View in: PubMed
    Score: 0.006
  30. 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: 0.006
  31. Targeted suppression of mTORC2 reduces seizures across models of epilepsy. Nat Commun. 2023 11 14; 14(1):7364.
    View in: PubMed
    Score: 0.006
  32. Remote neuronal activity drives glioma progression through SEMA4F. Nature. 2023 Jul; 619(7971):844-850.
    View in: PubMed
    Score: 0.006
  33. 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: 0.006
  34. Glioma epileptiform activity and progression are driven by IGSF3-mediated potassium dysregulation. Neuron. 2023 03 01; 111(5):682-695.e9.
    View in: PubMed
    Score: 0.006
  35. The Role of Hyperexcitability in Gliomagenesis. Int J Mol Sci. 2023 Jan 01; 24(1).
    View in: PubMed
    Score: 0.006
  36. Exploring new gene discoveries in idiopathic generalized epilepsy. Epilepsia. 2003; 44 Suppl 2:16-21.
    View in: PubMed
    Score: 0.006
  37. The biology of epilepsy genes. Annu Rev Neurosci. 2003; 26:599-625.
    View in: PubMed
    Score: 0.006
  38. Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects. Dis Model Mech. 2022 09 01; 15(9).
    View in: PubMed
    Score: 0.006
  39. Sodium channel gene expression and epilepsy. Novartis Found Symp. 2002; 241:109-20; discussion 120-3, 226-32.
    View in: PubMed
    Score: 0.005
  40. Absence of hippocampal mossy fiber sprouting in transgenic mice overexpressing brain-derived neurotrophic factor. J Neurosci Res. 2001 May 01; 64(3):268-76.
    View in: PubMed
    Score: 0.005
  41. Early 17?-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX). Neurobiol Dis. 2021 06; 153:105329.
    View in: PubMed
    Score: 0.005
  42. A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene family. Genomics. 2001 Feb 01; 71(3):339-50.
    View in: PubMed
    Score: 0.005
  43. Modeling human epilepsies in mice. Epilepsia. 2001; 42 Suppl 5:11-5.
    View in: PubMed
    Score: 0.005
  44. Benign focal epilepsies of childhood: genetically determined pathophysiology. Report of an international workshop. Epilepsia. 2000 Aug; 41(8):1049-50.
    View in: PubMed
    Score: 0.005
  45. Calcium channel defects in models of inherited generalized epilepsy. Epilepsia. 2000 Aug; 41(8):1074-5.
    View in: PubMed
    Score: 0.005
  46. Ion channels and epilepsy in man and mouse. Curr Opin Genet Dev. 2000 Jun; 10(3):286-91.
    View in: PubMed
    Score: 0.005
  47. Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13. Epilepsia. 2000 Jan; 41(1):24-7.
    View in: PubMed
    Score: 0.005
  48. Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication. Genome Res. 1999 Dec; 9(12):1204-13.
    View in: PubMed
    Score: 0.005
  49. Therapeutic inhibition of mTORC2 rescues the behavioral and neurophysiological abnormalities associated with Pten-deficiency. Nat Med. 2019 11; 25(11):1684-1690.
    View in: PubMed
    Score: 0.005
  50. Single gene defects in mice: the role of voltage-dependent calcium channels in absence models. Epilepsy Res. 1999 Sep; 36(2-3):111-22.
    View in: PubMed
    Score: 0.005
  51. 2017 WONOEP appraisal: Studying epilepsy as a network disease using systems biology approaches. Epilepsia. 2019 06; 60(6):1045-1053.
    View in: PubMed
    Score: 0.004
  52. Overexpression of a Shaker-type potassium channel in mammalian central nervous system dysregulates native potassium channel gene expression. Proc Natl Acad Sci U S A. 1999 Mar 02; 96(5):2451-5.
    View in: PubMed
    Score: 0.004
  53. Cortin disaster: lissencephaly genes spell double trouble for the developing brain. Ann Neurol. 1999 Feb; 45(2):141-2.
    View in: PubMed
    Score: 0.004
  54. Single-gene models of epilepsy. Adv Neurol. 1999; 79:227-38.
    View in: PubMed
    Score: 0.004
  55. Asynchronous suppression of visual cortex during absence seizures in stargazer mice. Nat Commun. 2018 05 16; 9(1):1938.
    View in: PubMed
    Score: 0.004
  56. Silent hippocampal seizures and spikes identified by foramen ovale electrodes in Alzheimer's disease. Nat Med. 2017 Jun; 23(6):678-680.
    View in: PubMed
    Score: 0.004
  57. Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse. Cell. 1997 Feb 07; 88(3):385-92.
    View in: PubMed
    Score: 0.004
  58. Identification of diverse astrocyte populations and their malignant analogs. Nat Neurosci. 2017 Mar; 20(3):396-405.
    View in: PubMed
    Score: 0.004
  59. Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein. Nat Commun. 2017 01 20; 8:14152.
    View in: PubMed
    Score: 0.004
  60. Neurogenetic approaches to axon sprouting in the hippocampus. Adv Neurol. 1997; 72:35-44.
    View in: PubMed
    Score: 0.004
  61. Ankyrin-G isoform imbalance and interneuronopathy link epilepsy and bipolar disorder. Mol Psychiatry. 2017 10; 22(10):1464-1472.
    View in: PubMed
    Score: 0.004
  62. 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: 0.004
  63. Epileptic Seizures in Alzheimer Disease: A Review. Alzheimer Dis Assoc Disord. 2016 Apr-Jun; 30(2):186-92.
    View in: PubMed
    Score: 0.004
  64. Targeting epilepsy genes. Neuron. 1996 Feb; 16(2):241-4.
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    Score: 0.004
  65. Molecular and cellular plasticity in developing epileptic brain. Cold Spring Harb Symp Quant Biol. 1996; 61:319-26.
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    Score: 0.004
  66. Sudden unexpected death in epilepsy: Identifying risk and preventing mortality. Epilepsia. 2015 Nov; 56(11):1700-6.
    View in: PubMed
    Score: 0.003
  67. Expression and function of Kv1.1 potassium channels in human atria from patients with atrial fibrillation. Basic Res Cardiol. 2015 Sep; 110(5):505.
    View in: PubMed
    Score: 0.003
  68. Genetic suppression of transgenic APP rescues Hypersynchronous network activity in a mouse model of Alzeimer's disease. J Neurosci. 2014 Mar 12; 34(11):3826-40.
    View in: PubMed
    Score: 0.003
  69. High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile. Epilepsia. 2014 Feb; 55(2):e6-12.
    View in: PubMed
    Score: 0.003
  70. Issues related to development of new antiseizure treatments. Epilepsia. 2013 Aug; 54 Suppl 4:24-34.
    View in: PubMed
    Score: 0.003
  71. 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: 0.003
  72. Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spots. J Mol Diagn. 2013 May; 15(3):283-90.
    View in: PubMed
    Score: 0.003
  73. Ion channels in genetic and acquired forms of epilepsy. J Physiol. 2013 Feb 15; 591(4):753-64.
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    Score: 0.003
  74. Comparative analytical utility of DNA derived from alternative human specimens for molecular autopsy and diagnostics. J Mol Diagn. 2012 Sep; 14(5):451-7.
    View in: PubMed
    Score: 0.003
  75. WONOEP XI: Workshop summary by the Scientific Organizing Committee. Epilepsia. 2012 Jul; 53(7):1275-6.
    View in: PubMed
    Score: 0.003
  76. Ablation of steroid receptor coactivator-3 resembles the human CACT metabolic myopathy. Cell Metab. 2012 May 02; 15(5):752-63.
    View in: PubMed
    Score: 0.003
  77. Identification of new epilepsy treatments: issues in preclinical methodology. Epilepsia. 2012 Mar; 53(3):571-82.
    View in: PubMed
    Score: 0.003
  78. 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: 0.003
  79. 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: 0.003
  80. Deletion of the potassium channel Kv12.2 causes hippocampal hyperexcitability and epilepsy. Nat Neurosci. 2010 Sep; 13(9):1056-8.
    View in: PubMed
    Score: 0.002
  81. Genetic testing in the epilepsies--report of the ILAE Genetics Commission. Epilepsia. 2010 Apr; 51(4):655-70.
    View in: PubMed
    Score: 0.002
  82. Curing epilepsy: progress and future directions. Epilepsy Behav. 2009 Mar; 14(3):438-45.
    View in: PubMed
    Score: 0.002
  83. Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization. J Physiol. 2008 Jul 15; 586(14):3405-23.
    View in: PubMed
    Score: 0.002
  84. 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: 0.002
  85. Genetics of epilepsy: epilepsy research foundation workshop report. Epileptic Disord. 2007 Jun; 9(2):194-236.
    View in: PubMed
    Score: 0.002
  86. A mouse model for Glut-1 haploinsufficiency. Hum Mol Genet. 2006 Apr 01; 15(7):1169-79.
    View in: PubMed
    Score: 0.002
  87. Mutational analysis of inherited epilepsies. Adv Neurol. 1986; 44:97-113.
    View in: PubMed
    Score: 0.002
  88. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. Hum Mol Genet. 2004 Nov 01; 13(21):2679-89.
    View in: PubMed
    Score: 0.002
  89. Cathepsin B but not cathepsins L or S contributes to the pathogenesis of Unverricht-Lundborg progressive myoclonus epilepsy (EPM1). J Neurobiol. 2003 Sep 15; 56(4):315-27.
    View in: PubMed
    Score: 0.002
  90. Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance. Mol Cell Biol. 2003 May; 23(10):3646-55.
    View in: PubMed
    Score: 0.001
  91. Models for epilepsy and epileptogenesis: report from the NIH workshop, Bethesda, Maryland. Epilepsia. 2002 Nov; 43(11):1410-20.
    View in: PubMed
    Score: 0.001
  92. ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies. Epilepsia. 2002 Oct; 43(10):1262-7.
    View in: PubMed
    Score: 0.001
  93. Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron. 2002 Jul 18; 35(2):243-54.
    View in: PubMed
    Score: 0.001
  94. Males with epilepsy, complete subcortical band heterotopia, and somatic mosaicism for DCX. Neurology. 2002 May 28; 58(10):1559-62.
    View in: PubMed
    Score: 0.001
  95. Future directions for epilepsy research. Neurology. 2001 Nov 13; 57(9):1536-42.
    View in: PubMed
    Score: 0.001
  96. 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: 0.001
  97. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet. 2000 Oct; 26(2):191-4.
    View in: PubMed
    Score: 0.001
  98. Analysis of inherited epilepsy using single locus mutations in mice. Fed Proc. 1979 Sep; 38(10):2405-10.
    View in: PubMed
    Score: 0.001
  99. 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: 0.001
  100. Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice. Nat Genet. 1998 Nov; 20(3):251-8.
    View in: PubMed
    Score: 0.001
  101. Cortical slow potentials and the occipital EEG in congenital blindness. J Neurol Sci. 1978 Jun; 37(1-2):51-8.
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    Score: 0.001
  102. A candidate model for Angelman syndrome in the mouse. Mamm Genome. 1997 Jul; 8(7):472-8.
    View in: PubMed
    Score: 0.001
  103. Genetic mapping and evaluation of candidate genes for spasmodic, a neurological mouse mutation with abnormal startle response. Genomics. 1993 Aug; 17(2):279-86.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

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