Developmental Neurogenetics Laboratory

Click on the Expand plus sign sign to list the book chapters and other publications by year. Then click on the link for details of that publication.

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  • Aiba I, Noebels J. The genetic borderland of migraine and epilepsy. In: Dalkara T, Moskowitz MA, editors. Neurobiological basis of migraine. Wiley-Blackwell; 2017. p. 209-231.
  • Goldman AM, Buchanan G, Aiba I, Noebels JL. SUDEP animal models. In: Pitkänen A, Buckmaster PS, Galanopoulou AS, Moshé SL, editors. Models of seizures and epilepsy. Academic Press; 2017. p. 1007-1018.
  • Krishnan V, Benatar M, Drislane FW. Cognitive manifestations of focal status epilepticus. In: Drislane FW, Kaplan PW, editors. Status epilepticus: A clinical perspective. 2nd ed. Springer Sciences; 2017. p. 259-274.
  • Krishnan V, Chang BS, Schomer DL. Normal EEG in wakefulness and sleep: Adults and elderly. In: Schomer DL, Lopes da Silva FH, editors. Niedermeyer's electroencephalography: Basic principles, clinical applications, and related fields. 7th ed. Oxford: Oxford University Press; 2017. p. 202-228.
  • Krishnan V, Chang BS, Schomer DL. The application of EEG to epilepsy in adults and elderly. In: Schomer DL, Lopes da Silva FH, editors. Niedermeyer's electroencephalography: Basic principles, clinical applications, and related fields. 7th ed. Oxford: Oxford University Press; 2017. p. 521-535.
  • Goldman A, Maheshwari A. Genetics of clinical epilepsy practice. In: Haneef Z, Maheshwari A, editors. A concise manual of epilepsy. 2nd ed. CreateSpace Publishing; 2016. p. 144-155.
  • Holmes GL, Noebels JL. The epilepsy spectrum: Targeting future research challenges. In: Holmes GL, Noebels JL, editors. Epilepsy: The biology of a spectrum disorder. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 2016. p. 439-450.
  • Noebels JL. Single-gene determinants of epilepsy comorbidity. In: Holmes GL, Noebels JL, editors. Epilepsy: The biology of a spectrum disorder. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 2016. p. 331-344.
  • Maheshwari A, Noebels JL. Monogenic models of absence epilepsy: Windows into the complex balance between inhibition and excitation in thalamocortical microcircuits. In: Steinlein OK, editor. Genetics of epilepsy. Progress in brain research. Vol. 213. Amsterdam: Elsevier; 2014. p. 223-252. Available from: https://www.sciencedirect.com/science/article/pii/B9780444633262000120. [view publication]
  • Noebels JL. The voltage-gated calcium channel and absence epilepsy. In: Noebels J, Avoli M, Rogawski M, Olsen R, Delgado-Escueta A, editors. Jasper's basic mechanisms of the epilepsies. 4th ed. New York: Oxford University Press; 2012. p. 702-13.
  • Goldman A. Basic mechanisms of SUDEP. In: Chapman D, Panelli R, Hanna J, Jeffs T, editors. Sudden unexpected death in epilepsy: continuing the global conversation. Camberwell, Australia: Epilepsy Australia, Epilepsy Bereaved & SUDEP Aware; 2011.
  • Noebels JL. Genes and the biology of complex epilepsy phenotypes. In: Avanzini G, Noebels J, editors. Genetics of epilepsy and genetic epilepsies. Montrouge, France: John Libbey Eurotext; 2009. p. 23-30.
  • Noebels JL. Spontaneous epileptic mutations in the mouse. In: Pitkanen A, Schwartzkroin PA, Moshe SL, editors. Models of seizures and epilepsy. Boston: Elsevier Academic Press; 2006. p. 223-232.
  • Noebels JL. Sodium channel gene expression and epilepsy. In: Novartis Foundation , editor. Sodium channels and neuronal hyperexcitability. New York: John Wiley & Sons, LTD.; 2002. p. 109-123.
  • Noebels JL. Genetic and phenotypic heterogeneity of inherited spike-and-wave epilepsies. In: Malafosse A, Genton P, Hirsch E, Marescaux C, Broglin D, Bernasconi R, editors. Idiopathic generalized epilepsies: Clinical, experimental and genetic aspects. London: John Libbey; 1994. p. 215-225.